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Carcinoma de células renais
ORPHA:217071CID-10 · C64CID-11 · 2C90.0DOENÇA RARA
Esta doença tem causa genética. Recomendamos procurar um médico geneticista para diagnóstico, exames genéticos e aconselhamento familiar.
Visão / ocularInício adultaHerança Unknown
Também conhecida comoCarcinoma de célula renalCarcinoma das células renaisCâncer no rimCâncer de rimRCC

Carcinoma que surge das células epiteliais glandulares do rim

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Introdução

O que você precisa saber de cara

💬
EM LINGUAGEM SIMPLES

O carcinoma de células renais é um tipo de câncer que se desenvolve nas células epiteliais dos rins, afetando principalmente pessoas adultas. Além do tumor renal, o quadro pode vir acompanhado de pressão alta, palpitações, fraqueza nos músculos, suor excessivo e alterações hormonais ou na visão. Diversas alterações genéticas podem estar associadas à doença, como alterações nos genes VHL, FLCN e TERT. No Brasil, o tratamento pelo SUS é conduzido conforme a autonomia de cada serviço de saúde credenciado, seguindo as diretrizes diagnósticas estabelecidas.

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Informacoes curadas por IA — podem conter imprecisoes

Carcinoma que surge das células epiteliais glandulares do rim

Pesquisas ativas
495 ensaios
1998 total registrados no ClinicalTrials.gov
Publicações científicas
53.101 artigos
Último publicado: 2026
Medicamentos
3 com registro
Everolimus (EVEROLIMUS), Sunitinib Malate (SUNITINIB MALATE), KEYTRUDA QLEX (PEMBROLIZUMAB AND BERAHYALURONIDASE ALFA-PMPH)

Tem tratamento?

✓ 3 medicamentos específicos desta doença (registro ANVISA, FDA ou SUS/CEAF)
Ver detalhes, fases e interações →
EVEROLIMUS (EVEROLIMUS)SUNITINIB MALATE (SUNITINIB MALATE)KEYTRUDA QLEX (PEMBROLIZUMAB AND BERAHYALURONIDASE ALFA-PMPH)

Escala de raridade

CLASSIFICAÇÃO ORPHANET · BRASIL 2024
1-5 / 10 000
Ultra-rara
<1/50k
Muito rara
1/20k
Rara
1/10k
Pouco freq.
1/5k
Incomum
1/2k
Prevalência
42.0
Europe
Início
Adult
🏥
SUS: Sem cobertura SUSScore: 0%
CID-10: C64
Você se identifica com essa condição?
O Raras está aqui pra te apoiar — com ou sem diagnóstico

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Entender a doença

Do básico ao detalhe, leia no seu ritmo

Preparando trilha educativa...

Sinais e sintomas

O que aparece no corpo e com que frequência cada sintoma acontece

Partes do corpo afetadas

👁️
Olhos
12 sintomas
🫘
Rins
4 sintomas
📏
Crescimento
3 sintomas
🧠
Neurológico
2 sintomas
🫁
Pulmão
1 sintomas
💪
Músculos
1 sintomas

+ 24 sintomas em outras categorias

Características mais comuns

—
Acuidade visual reduzida
—
Catarata
—
Aumento do nível urinário de cortisol
—
Aumento do estradiol sérico
—
Nistagmo congênito
—
Palpitações
49sintomas
Sem dados (49)

Os sintomas variam de pessoa para pessoa. Abaixo estão as 49 características clínicas mais associadas, ordenadas por frequência.

Acuidade visual reduzidaReduced visual acuity
CatarataCataract
Aumento do nível urinário de cortisolIncreased urinary cortisol level
Aumento do estradiol séricoIncreased serum estradiol
Nistagmo congênitoCongenital nystagmus

Linha do tempo da pesquisa

Publicações por ano — veja quando o interesse científico cresceu
Anos de pesquisa1desde 2026
Total histórico53.101PubMed
Últimos 10 anos200publicações
Pico2026199 papers
Linha do tempo
2026Hoje · 2026🧪 1990Primeiro ensaio clínico
Publicações por ano (últimos 10 anos)

Encontrou um erro ou informação desatualizada? Sugira uma correção →

Genética e causas

O que está alterado no DNA e como passa nas famílias

Genes associados

30 genes identificados com associação a esta condição. Padrão de herança: Not applicable.

Curadoria gene-doença

fontes oficiais
BAP1SDHBVHL
TERTTelomerase reverse transcriptaseCandidate gene tested inRestrito
VIAS BIOLÓGICAS (3)
Telomere Extension By TelomeraseFormation of the beta-catenin:TCF transactivating complexRegulation of MITF-M-dependent genes involved in DNA replication, damage repair and senescence
EXPRESSÃO TECIDUAL(Baixa expressão)
Testículo
2.7 TPM
Intestino delgado
0.7 TPM
Brain Caudate basal ganglia
0.6 TPM
Cólon transverso
0.5 TPM
Brain Nucleus accumbens basal ganglia
0.5 TPM
OUTRAS DOENÇAS (13)
dyskeratosis congenita, autosomal dominant 2pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1adrenal cortex carcinomaclear cell sarcoma of kidney
HGNC:11730UniProt:O14746
CLTCClathrin heavy chain 1Candidate gene tested inAltamente restrito
VIAS BIOLÓGICAS (10)
Gap junction degradationFormation of annular gap junctionsEPH-ephrin mediated repulsion of cellsEntry of Influenza Virion into Host Cell via EndocytosisRetrograde neurotrophin signalling
MECANISMO DE DOENÇA

Intellectual developmental disorder, autosomal dominant 56

A form of intellectual disability, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period.

OUTRAS DOENÇAS (5)
intellectual disability, autosomal dominant 56inflammatory myofibroblastic tumorMIT family translocation renal cell carcinomaundetermined early-onset epileptic encephalopathy
HGNC:2092UniProt:Q00610
HNF1AHepatocyte nuclear factor 1-alphaDisease-causing germline mutation(s) inAltamente restrito
VIAS BIOLÓGICAS (1)
Regulation of gene expression in beta cells
MECANISMO DE DOENÇA

Hepatic adenomas familial

Rare benign liver tumors of presumable epithelial origin that develop in an otherwise normal liver. Hepatic adenomas may be single or multiple. They consist of sheets of well-differentiated hepatocytes that contain fat and glycogen and can produce bile. Bile ducts or portal areas are absent. Kupffer cells, if present, are reduced in number and are non-functional. Conditions associated with adenomas are insulin-dependent diabetes mellitus and glycogen storage diseases (types 1 and 3).

EXPRESSÃO TECIDUAL(Tecido-específico)
Fígado
8.7 TPM
Intestino delgado
6.3 TPM
Rim - Córtex
5.3 TPM
Cólon transverso
4.3 TPM
Estômago
4.1 TPM
OUTRAS DOENÇAS (11)
maturity-onset diabetes of the young type 3nonpapillary renal cell carcinomahepatic adenomas, familialtype 1 diabetes mellitus 20
HGNC:11621UniProt:P20823
OGG1N-glycosylase/DNA lyaseDisease-causing germline mutation(s) inTolerante
VIAS BIOLÓGICAS (6)
Cleavage of the damaged purineRecognition and association of DNA glycosylase with site containing an affected purineCleavage of the damaged pyrimidine APEX1-Independent Resolution of AP Sites via the Single Nucleotide Replacement PathwayDisplacement of DNA glycosylase by APEX1
MECANISMO DE DOENÇA

Renal cell carcinoma

Renal cell carcinoma is a heterogeneous group of sporadic or hereditary carcinoma derived from cells of the proximal renal tubular epithelium. It is subclassified into clear cell renal carcinoma (non-papillary carcinoma), papillary renal cell carcinoma, chromophobe renal cell carcinoma, collecting duct carcinoma with medullary carcinoma of the kidney, and unclassified renal cell carcinoma. Clear cell renal cell carcinoma is the most common subtype.

EXPRESSÃO TECIDUAL(Ubíquo)
Ovário
23.6 TPM
Útero
23.3 TPM
Cervix Endocervix
22.6 TPM
Cervix Ectocervix
21.7 TPM
Nervo tibial
19.6 TPM
OUTRAS DOENÇAS (2)
nonpapillary renal cell carcinomahereditary clear cell renal cell carcinoma
HGNC:8125UniProt:O15527
CTNNB1Catenin beta-1Candidate gene tested inAltamente restrito
VIAS BIOLÓGICAS (10)
Formation of the nephric ductSpecification of the neural plate borderSynthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1)TCF dependent signaling in response to WNTTranscriptional Regulation by VENTX
MECANISMO DE DOENÇA

Colorectal cancer

A complex disease characterized by malignant lesions arising from the inner wall of the large intestine (the colon) and the rectum. Genetic alterations are often associated with progression from premalignant lesion (adenoma) to invasive adenocarcinoma. Risk factors for cancer of the colon and rectum include colon polyps, long-standing ulcerative colitis, and genetic family history.

EXPRESSÃO TECIDUAL(Ubíquo)
Cervix Endocervix
297.5 TPM
Cervix Ectocervix
257.8 TPM
Artéria tibial
233.5 TPM
Ovário
201.9 TPM
Cérebro - Hemisfério cerebelar
201.3 TPM
OUTRAS DOENÇAS (17)
hepatocellular carcinomasevere intellectual disability-progressive spastic diplegia syndromeovarian cancerpilomatrixoma
HGNC:2514UniProt:P35222
DIRC3Candidate gene tested inDesconhecido
OUTRAS DOENÇAS (2)
differentiated thyroid carcinomahereditary clear cell renal cell carcinoma
HGNC:17805
VHLvon Hippel-Lindau disease tumor suppressorDisease-causing germline mutation(s) inTolerante
VIAS BIOLÓGICAS (6)
Antigen processing: Ubiquitination & Proteasome degradationOxygen-dependent proline hydroxylation of Hypoxia-inducible Factor AlphaNeddylationReplication of the SARS-CoV-1 genomeReplication of the SARS-CoV-2 genome
MECANISMO DE DOENÇA

Pheochromocytoma

A catecholamine-producing tumor of chromaffin tissue of the adrenal medulla or sympathetic paraganglia. The cardinal symptom, reflecting the increased secretion of epinephrine and norepinephrine, is hypertension, which may be persistent or intermittent.

EXPRESSÃO TECIDUAL(Ubíquo)
Linfócitos
47.6 TPM
Fibroblastos
30.1 TPM
Cérebro - Hemisfério cerebelar
29.8 TPM
Baço
24.1 TPM
Cervix Endocervix
22.7 TPM
OUTRAS DOENÇAS (6)
pheochromocytomavon Hippel-Lindau diseasenonpapillary renal cell carcinomaChuvash polycythemia
HGNC:12687UniProt:P40337
FHITBis(5'-adenosyl)-triphosphataseCandidate gene tested inTolerante
EXPRESSÃO TECIDUAL(Ubíquo)
Glândula adrenal
7.7 TPM
Tireoide
7.4 TPM
Rim - Medula
6.1 TPM
Brain Spinal cord cervical c-1
5.5 TPM
Rim - Córtex
5.0 TPM
OUTRAS DOENÇAS (1)
hereditary clear cell renal cell carcinoma
HGNC:3701UniProt:P49789
SLC49A4Solute carrier family 49 member 4Candidate gene tested inTolerante
INTERAÇÕES PROTEICAS (3)
OUTRAS DOENÇAS (1)
hereditary clear cell renal cell carcinoma
HGNC:16628UniProt:Q96SL1
ELP4Elongator complex protein 4Disease-causing germline mutation(s) inTolerante
VIAS BIOLÓGICAS (1)
HATs acetylate histones
MECANISMO DE DOENÇA

Aniridia 2

A form of aniridia, a congenital, bilateral, panocular disorder characterized by complete absence of the iris or extreme iris hypoplasia. Aniridia is not just an isolated defect in iris development but it is associated with macular and optic nerve hypoplasia, cataract, corneal changes, nystagmus. Visual acuity is generally low but is unrelated to the degree of iris hypoplasia. Glaucoma is a secondary problem causing additional visual loss over time.

VIAS REACTOME (1)
EXPRESSÃO TECIDUAL(Baixa expressão)
Cérebro - Hemisfério cerebelar
4.8 TPM
Cerebelo
4.1 TPM
Linfócitos
2.8 TPM
Nervo tibial
2.4 TPM
Artéria tibial
2.3 TPM
OUTRAS DOENÇAS (1)
aniridia 2
HGNC:HGNC:1171UniProt:Q96EB1
PRKAR1AcAMP-dependent protein kinase type I-alpha regulatory subunitCandidate gene tested inAltamente restrito
VIAS BIOLÓGICAS (10)
PKA activationGPER1 signalingCREB1 phosphorylation through the activation of Adenylate CyclaseDARPP-32 eventsHigh laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells
MECANISMO DE DOENÇA

Carney complex 1

CNC is a multiple neoplasia syndrome characterized by spotty skin pigmentation, cardiac and other myxomas, endocrine tumors, and psammomatous melanotic schwannomas.

EXPRESSÃO TECIDUAL(Ubíquo)
Artéria tibial
152.7 TPM
Ovário
151.5 TPM
Aorta
138.6 TPM
Útero
138.3 TPM
Tecido adiposo
129.4 TPM
OUTRAS DOENÇAS (9)
familial atrial myxomapigmented nodular adrenocortical disease, primary, 1Acrodysostosis 1 with or without hormone resistanceCarney complex, type 1
HGNC:9388UniProt:P10644
FLCNFolliculinDisease-causing germline mutation(s) inAltamente restrito
VIAS BIOLÓGICAS (1)
Amino acids regulate mTORC1
MECANISMO DE DOENÇA

Birt-Hogg-Dube syndrome 1

A form of Birt-Hogg-Dube syndrome, a rare genodermatosis usually manifesting in adulthood and characterized by multiple fibrofolliculomas, trichodiscomas, and acrochordons. Patients with this syndrome have an increased susceptibility to develop renal cell carcinoma, lung cysts, and spontaneous pneumothorax. Inheritance is autosomal dominant.

EXPRESSÃO TECIDUAL(Ubíquo)
Cerebelo
123.5 TPM
Cervix Ectocervix
117.5 TPM
Cérebro - Hemisfério cerebelar
109.7 TPM
Cervix Endocervix
83.8 TPM
Cólon sigmoide
69.3 TPM
OUTRAS DOENÇAS (5)
nonpapillary renal cell carcinomacolorectal cancerBirt-Hogg-Dube syndrome 1familial spontaneous pneumothorax
HGNC:27310UniProt:Q8NFG4
PBRM1Protein polybromo-1Disease-causing germline mutation(s) inAltamente restrito
VIAS BIOLÓGICAS (3)
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not knownRMTs methylate histone argininesFormation of the polybromo-BAF (pBAF) complex
MECANISMO DE DOENÇA

Renal cell carcinoma

Renal cell carcinoma is a heterogeneous group of sporadic or hereditary carcinoma derived from cells of the proximal renal tubular epithelium. It is subclassified into clear cell renal carcinoma (non-papillary carcinoma), papillary renal cell carcinoma, chromophobe renal cell carcinoma, collecting duct carcinoma with medullary carcinoma of the kidney, and unclassified renal cell carcinoma. Clear cell renal cell carcinoma is the most common subtype.

EXPRESSÃO TECIDUAL(Ubíquo)
Ovário
28.1 TPM
Útero
27.0 TPM
Fibroblastos
26.9 TPM
Artéria tibial
26.8 TPM
Nervo tibial
25.1 TPM
OUTRAS DOENÇAS (2)
nonpapillary renal cell carcinomaclear cell papillary renal cell carcinoma
HGNC:30064UniProt:Q86U86
MITFMicrophthalmia-associated transcription factorCandidate gene tested inAltamente restrito
VIAS BIOLÓGICAS (2)
Transcriptional and post-translational regulation of MITF-M expression and activitySUMOylation of transcription factors
MECANISMO DE DOENÇA

Waardenburg syndrome 2A

WS2 is a genetically heterogeneous, autosomal dominant disorder characterized by sensorineural deafness, pigmentary disturbances, and absence of dystopia canthorum. The frequency of deafness is higher in WS2 than in WS1.

EXPRESSÃO TECIDUAL(Ubíquo)
Cervix Ectocervix
70.8 TPM
Cervix Endocervix
58.0 TPM
Útero
57.6 TPM
Músculo esquelético
25.9 TPM
Esôfago - Muscular
24.4 TPM
OUTRAS DOENÇAS (9)
Waardenburg syndrome type 2ATietz syndromecoloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafnesspapillary renal cell carcinoma
HGNC:7105UniProt:O75030
HNF1BHepatocyte nuclear factor 1-betaCandidate gene tested inAltamente restrito
VIAS BIOLÓGICAS (6)
Nephron developmentRegulation of gene expression in early pancreatic precursor cellsRegulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cellsDevelopmental Lineage of Multipotent Pancreatic Progenitor CellsDevelopmental Lineage of Pancreatic Ductal Cells
MECANISMO DE DOENÇA

Renal cysts and diabetes syndrome

An autosomal dominant disorder comprising non-diabetic renal disease resulting from abnormal renal development, and diabetes, which in some cases occurs earlier than age 25 years and is thus consistent with a diagnosis of maturity-onset diabetes of the young (MODY5). The renal disease is highly variable and includes renal cysts, glomerular tufts, aberrant nephrogenesis, primitive tubules, irregular collecting systems, oligomeganephronia, enlarged renal pelves, abnormal calyces, small kidney, single kidney, horseshoe kidney, and hyperuricemic nephropathy. Affected individuals may also have abnormalities of the genital tract.

EXPRESSÃO TECIDUAL(Tecido-específico)
Rim - Medula
90.4 TPM
Rim - Córtex
53.5 TPM
Linfócitos
43.7 TPM
Pâncreas
23.0 TPM
Cólon transverso
14.9 TPM
OUTRAS DOENÇAS (11)
type 2 diabetes mellitusrenal cysts and diabetes syndromechromosome 17q12 deletion syndromerenal dysplasia, unilateral
HGNC:11630UniProt:P35680
CDKN2ACyclin-dependent kinase inhibitor 2ACandidate gene tested inRestrito
VIAS BIOLÓGICAS (8)
Regulation of TP53 DegradationOncogene Induced SenescenceOxidative Stress Induced SenescenceStabilization of p53Regulation of RUNX3 expression and activity
OUTRAS DOENÇAS (10)
B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)familial melanomaLi-Fraumeni syndromefamilial atypical multiple mole melanoma syndrome
HGNC:1787UniProt:P42771
ASPSCR1Tether containing UBX domain for GLUT4Candidate gene tested inTolerante
VIAS BIOLÓGICAS (1)
Translocation of SLC2A4 (GLUT4) to the plasma membrane
OUTRAS DOENÇAS (2)
alveolar soft part sarcomaMIT family translocation renal cell carcinoma
HGNC:13825UniProt:Q9BZE9
HSPBAP1HSPB1-associated protein 1Candidate gene tested inTolerante
EXPRESSÃO TECIDUAL(Ubíquo)
Baço
16.6 TPM
Tireoide
11.4 TPM
Testículo
10.5 TPM
Sangue
10.2 TPM
Cervix Endocervix
9.8 TPM
OUTRAS DOENÇAS (1)
hereditary clear cell renal cell carcinoma
HGNC:16389UniProt:Q96EW2
PAX6Paired box protein Pax-6Disease-causing germline mutation(s) inAltamente restrito
VIAS BIOLÓGICAS (5)
Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1)Regulation of gene expression in beta cellsActivation of anterior HOX genes in hindbrain development during early embryogenesisFormation of the anterior neural plateSynthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP)
MECANISMO DE DOENÇA

Aniridia 1

A congenital, bilateral, panocular disorder characterized by complete absence of the iris or extreme iris hypoplasia. Aniridia is not just an isolated defect in iris development but it is associated with macular and optic nerve hypoplasia, cataract, corneal changes, nystagmus. Visual acuity is generally low but is unrelated to the degree of iris hypoplasia. Glaucoma is a secondary problem causing additional visual loss over time.

EXPRESSÃO TECIDUAL(Tecido-específico)
Cérebro - Hemisfério cerebelar
40.8 TPM
Cerebelo
36.9 TPM
Córtex cerebral
3.5 TPM
Brain Caudate basal ganglia
3.4 TPM
Brain Anterior cingulate cortex BA24
3.3 TPM
OUTRAS DOENÇAS (17)
coloboma, ocular, autosomal dominantisolated optic nerve hypoplasiaautosomal dominant keratitisfoveal hypoplasia 1
HGNC:8620UniProt:P26367
ZNRF3E3 ubiquitin-protein ligase ZNRF3Candidate gene tested inAltamente restrito
VIAS BIOLÓGICAS (1)
Regulation of FZD by ubiquitination
EXPRESSÃO TECIDUAL(Ubíquo)
Cérebro - Hemisfério cerebelar
15.1 TPM
Cerebelo
15.1 TPM
Aorta
13.1 TPM
Artéria tibial
12.4 TPM
Córtex cerebral
11.3 TPM
OUTRAS DOENÇAS (1)
adrenal cortex carcinoma
HGNC:18126UniProt:Q9ULT6
NONONon-POU domain-containing octamer-binding proteinCandidate gene tested inAltamente restrito
EXPRESSÃO TECIDUAL(Ubíquo)
Linfócitos
238.9 TPM
Ovário
222.1 TPM
Fibroblastos
181.7 TPM
Útero
171.6 TPM
Cervix Endocervix
164.9 TPM
OUTRAS DOENÇAS (2)
syndromic X-linked intellectual disability 34MIT family translocation renal cell carcinoma
HGNC:7871UniProt:Q15233
SFPQSplicing factor, proline- and glutamine-richCandidate gene tested inAltamente restrito
VIAS BIOLÓGICAS (1)
PTK6 Regulates Proteins Involved in RNA Processing
EXPRESSÃO TECIDUAL(Ubíquo)
Ovário
224.7 TPM
Nervo tibial
185.7 TPM
Cérebro - Hemisfério cerebelar
181.1 TPM
Linfócitos
173.0 TPM
Útero
167.4 TPM
OUTRAS DOENÇAS (1)
MIT family translocation renal cell carcinoma
HGNC:10774UniProt:P23246
TFEBTranscription factor EBCandidate gene tested inAltamente restrito
VIAS BIOLÓGICAS (2)
Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock genesTranscriptional and post-translational regulation of MITF-M expression and activity
EXPRESSÃO TECIDUAL(Ubíquo)
Linfócitos
58.4 TPM
Sangue
36.1 TPM
Baço
34.6 TPM
Brain Spinal cord cervical c-1
26.0 TPM
Músculo esquelético
25.8 TPM
OUTRAS DOENÇAS (1)
MIT family translocation renal cell carcinoma
HGNC:11753UniProt:P19484
TP53Cellular tumor antigen p53Candidate gene tested inAltamente restrito
VIAS BIOLÓGICAS (10)
TP53 Regulates Metabolic GenesRegulation of TP53 ExpressionRegulation of TP53 DegradationOncogene Induced SenescenceOxidative Stress Induced Senescence
EXPRESSÃO TECIDUAL(Ubíquo)
Linfócitos
73.0 TPM
Skin Sun Exposed Lower leg
37.0 TPM
Skin Not Sun Exposed Suprapubic
35.2 TPM
Fibroblastos
32.9 TPM
Ovário
32.4 TPM
OUTRAS DOENÇAS (29)
Li-Fraumeni syndromenasopharyngeal carcinoma, susceptibility to, 1hepatocellular carcinomafamilial pancreatic carcinoma
HGNC:11998UniProt:P04637
PRCCProline-rich protein PRCCDisease-causing germline mutation(s) inAltamente restrito
VIAS BIOLÓGICAS (2)
mRNA Splicing - Major PathwayDengue Virus-Host Interactions
EXPRESSÃO TECIDUAL(Ubíquo)
Linfócitos
73.8 TPM
Cérebro - Hemisfério cerebelar
72.8 TPM
Útero
72.8 TPM
Cerebelo
71.1 TPM
Cervix Endocervix
70.9 TPM
OUTRAS DOENÇAS (2)
hereditary papillary renal cell carcinomaMIT family translocation renal cell carcinoma
HGNC:9343UniProt:Q92733
METHepatocyte growth factor receptorDisease-causing germline mutation(s) inAltamente restrito
VIAS BIOLÓGICAS (7)
MET Receptor ActivationDrug-mediated inhibition of MET activationSema4D mediated inhibition of cell attachment and migrationNegative regulation of MET activityMECP2 regulates neuronal receptors and channels
EXPRESSÃO TECIDUAL(Ubíquo)
Nervo tibial
21.3 TPM
Fibroblastos
18.5 TPM
Tireoide
16.7 TPM
Adipose Visceral Omentum
16.2 TPM
Mama
15.4 TPM
OUTRAS DOENÇAS (8)
hepatocellular carcinomahereditary papillary renal cell carcinomaarthrogryposis, distal, IIa 11autosomal recessive nonsyndromic hearing loss 97
HGNC:7029UniProt:P08581
TRIM44Tripartite motif-containing protein 44Disease-causing germline mutation(s) inRestrito
MECANISMO DE DOENÇA

Aniridia 3

A form of aniridia, a congenital, bilateral, panocular disorder characterized by complete absence of the iris or extreme iris hypoplasia. Aniridia is not just an isolated defect in iris development but it is associated with macular and optic nerve hypoplasia, cataract, corneal changes, nystagmus. Visual acuity is generally low but is unrelated to the degree of iris hypoplasia. Glaucoma is a secondary problem causing additional visual loss over time.

EXPRESSÃO TECIDUAL(Ubíquo)
Cérebro - Hemisfério cerebelar
53.8 TPM
Cerebelo
52.3 TPM
Fibroblastos
33.5 TPM
Linfócitos
32.5 TPM
Nervo tibial
30.5 TPM
INTERAÇÕES PROTEICAS (5)
OUTRAS DOENÇAS (2)
aniridia 3isolated aniridia
HGNC:19016UniProt:Q96DX7
RNF139E3 ubiquitin-protein ligase RNF139Disease-causing germline mutation(s) inAltamente restrito
VIAS BIOLÓGICAS (1)
ER Quality Control Compartment (ERQC)
MECANISMO DE DOENÇA

Renal cell carcinoma

Renal cell carcinoma is a heterogeneous group of sporadic or hereditary carcinoma derived from cells of the proximal renal tubular epithelium. It is subclassified into clear cell renal carcinoma (non-papillary carcinoma), papillary renal cell carcinoma, chromophobe renal cell carcinoma, collecting duct carcinoma with medullary carcinoma of the kidney, and unclassified renal cell carcinoma. Clear cell renal cell carcinoma is the most common subtype.

EXPRESSÃO TECIDUAL(Ubíquo)
Testículo
111.7 TPM
Fibroblastos
43.0 TPM
Fallopian Tube
42.1 TPM
Ovário
40.0 TPM
Útero
37.8 TPM
OUTRAS DOENÇAS (2)
nonpapillary renal cell carcinomahereditary clear cell renal cell carcinoma
HGNC:17023UniProt:Q8WU17
TFE3Transcription factor E3Disease-causing germline mutation(s) inAltamente restrito
VIAS BIOLÓGICAS (1)
Transcriptional and post-translational regulation of MITF-M expression and activity
MECANISMO DE DOENÇA

Intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies

A disorder characterized by severe developmental delay with impaired intellectual development and poor speech, coarse facial dysmorphisms, and Blaschkoid pigmentary mosaicism. Additional clinical features may include epilepsy, orthopedic abnormalities, hypotonia, and growth abnormalities. The disorder affects both males and females.

EXPRESSÃO TECIDUAL(Ubíquo)
Fallopian Tube
116.0 TPM
Útero
109.4 TPM
Nervo tibial
107.4 TPM
Cervix Ectocervix
103.1 TPM
Sangue
102.7 TPM
OUTRAS DOENÇAS (5)
intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse faciesrenal cell carcinoma, Xp11-associatedalveolar soft part sarcomaMIT family translocation renal cell carcinoma
HGNC:11752UniProt:P19532
TMEM127Transmembrane protein 127Candidate gene tested inTolerante
MECANISMO DE DOENÇA

Pheochromocytoma

A catecholamine-producing tumor of chromaffin tissue of the adrenal medulla or sympathetic paraganglia. The cardinal symptom, reflecting the increased secretion of epinephrine and norepinephrine, is hypertension, which may be persistent or intermittent.

EXPRESSÃO TECIDUAL(Ubíquo)
Aorta
52.3 TPM
Bladder
48.8 TPM
Artéria tibial
48.4 TPM
Cervix Endocervix
47.4 TPM
Skin Sun Exposed Lower leg
47.0 TPM
OUTRAS DOENÇAS (3)
hereditary pheochromocytoma-paragangliomaclear cell papillary renal cell carcinomapheochromocytoma
HGNC:26038UniProt:O75204

Medicamentos aprovados (FDA)

3 medicamentos encontrados nos registros da FDA americana.

💊 Everolimus (EVEROLIMUS)
💊 Sunitinib Malate (SUNITINIB MALATE)
💊 KEYTRUDA QLEX (PEMBROLIZUMAB AND BERAHYALURONIDASE ALFA-PMPH)
Ver no DailyMed/FDA

Variantes genéticas (ClinVar)

1.376 variantes patogênicas registradas no ClinVar.

🧬 TERT: GRCh38/hg38 5p15.33-15.32(chr5:113462-5578808)x1 ()
🧬 TERT: NM_198253.3(TERT):c.3221G>A (p.Cys1074Tyr) ()
🧬 TERT: NM_198253.3(TERT):c.262del (p.Leu88fs) ()
🧬 TERT: NM_198253.3(TERT):c.198_207dup (p.Ser70fs) ()
🧬 TERT: NM_198253.3(TERT):c.11_27dup (p.Val10fs) ()
Ver todas no ClinVar

Classificação de variantes (ClinVar)

Distribuição de 32.171 variantes classificadas pelo ClinVar.

24128
8043
VUS (75.0%)
Benigna (25.0%)
VARIANTES MAIS SIGNIFICATIVAS
MET: NM_000245.4(MET):c.3467T>G (p.Val1156Gly) [Uncertain significance]
MET: NM_000245.4(MET):c.1595C>T (p.Ala532Val) [Uncertain significance]
MET: NM_000245.4(MET):c.2539C>G (p.Pro847Ala) [Uncertain significance]
MET: NM_000245.4(MET):c.935A>T (p.Glu312Val) [Uncertain significance]
MET: NM_000245.4(MET):c.2512A>G (p.Asn838Asp) [Uncertain significance]

Vias biológicas (Reactome)

165 vias biológicas associadas aos genes desta condição.

Telomere Extension By Telomerase Formation of the beta-catenin:TCF transactivating complex Regulation of MITF-M-dependent genes involved in DNA replication, damage repair and senescence Entry of Influenza Virion into Host Cell via Endocytosis Retrograde neurotrophin signalling Gap junction degradation Formation of annular gap junctions MHC class II antigen presentation EPH-ephrin mediated repulsion of cells Lysosome Vesicle Biogenesis Golgi Associated Vesicle Biogenesis Recycling pathway of L1 WNT5A-dependent internalization of FZD4 WNT5A-dependent internalization of FZD2, FZD5 and ROR2 Cargo recognition for clathrin-mediated endocytosis Clathrin-mediated endocytosis VLDLR internalisation and degradation LDL clearance RHOU GTPase cycle RHOV GTPase cycle ALK mutants bind TKIs Signaling by ALK fusions and activated point mutants Regulation of gene expression in beta cells Recognition and association of DNA glycosylase with site containing an affected pyrimidine Cleavage of the damaged pyrimidine Recognition and association of DNA glycosylase with site containing an affected purine Cleavage of the damaged purine Displacement of DNA glycosylase by APEX1 APEX1-Independent Resolution of AP Sites via the Single Nucleotide Replacement Pathway Defective OGG1 Substrate Binding Defective OGG1 Substrate Processing Defective OGG1 Localization Degradation of beta-catenin by the destruction complex Beta-catenin phosphorylation cascade TCF dependent signaling in response to WNT LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production Apoptotic cleavage of cell adhesion proteins Deactivation of the beta-catenin transactivating complex Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) Ca2+ pathway Adherens junctions interactions Binding of TCF/LEF:CTNNB1 to target gene promoters Disassembly of the destruction complex and recruitment of AXIN to the membrane VEGFR2 mediated vascular permeability Myogenesis Signaling by GSK3beta mutants CTNNB1 S33 mutants aren't phosphorylated CTNNB1 S37 mutants aren't phosphorylated CTNNB1 S45 mutants aren't phosphorylated CTNNB1 T41 mutants aren't phosphorylated RHO GTPases activate IQGAPs Transcriptional Regulation by VENTX InlA-mediated entry of Listeria monocytogenes into host cells RUNX3 regulates WNT signaling Cardiogenesis Germ layer formation at gastrulation Regulation of CDH11 function Regulation of CDH19 Expression and Function Regulation of CDH1 Function Degradation of CDH1 Regulation of CDH1 posttranslational processing and trafficking to plasma membrane Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha SUMOylation of ubiquitinylation proteins Neddylation Replication of the SARS-CoV-1 genome Replication of the SARS-CoV-2 genome RHOBTB3 ATPase cycle Antigen processing: Ubiquitination & Proteasome degradation Transcriptional regulation by RUNX3 HATs acetylate histones PKA activation PKA activation in glucagon signalling DARPP-32 events Glucagon-like Peptide-1 (GLP1) regulates insulin secretion Vasopressin regulates renal water homeostasis via Aquaporins CREB1 phosphorylation through the activation of Adenylate Cyclase Hedgehog 'off' state GPER1 signaling ADORA2B mediated anti-inflammatory cytokines production FCGR3A-mediated IL10 synthesis Factors involved in megakaryocyte development and platelet production High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells Amino acids regulate mTORC1 RMTs methylate histone arginines RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known Formation of the polybromo-BAF (pBAF) complex SUMOylation of transcription factors Regulation of MITF-M-dependent genes involved in pigmentation Regulation of MITF-M-dependent genes involved in apoptosis Regulation of MITF-M-dependent genes involved in cell cycle and proliferation Regulation of MITF-M dependent genes involved in metabolism Regulation of MITF-M dependent genes involved in invasion Transcriptional and post-translational regulation of MITF-M expression and activity Regulation of MITF-M-dependent genes involved in lysosome biogenesis and autophagy Regulation of MITF-M-dependent genes involved in extracellular matrix, focal adhesion and epithelial-to-mesenchymal transition Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells Regulation of gene expression in early pancreatic precursor cells Nephron development Developmental Lineage of Pancreatic Acinar Cells Developmental Lineage of Pancreatic Ductal Cells Developmental Lineage of Multipotent Pancreatic Progenitor Cells Oxidative Stress Induced Senescence Senescence-Associated Secretory Phenotype (SASP) Oncogene Induced Senescence Cyclin D associated events in G1 Evasion of Oncogene Induced Senescence Due to Defective p16INK4A binding to CDK4 Evasion of Oncogene Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6 Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4 Evasion of Oxidative Stress Induced Senescence Due to Defective p16INK4A binding to CDK4 and CDK6 Translocation of SLC2A4 (GLUT4) to the plasma membrane Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) Activation of anterior HOX genes in hindbrain development during early embryogenesis Formation of the anterior neural plate Regulation of FZD by ubiquitination PTK6 Regulates Proteins Involved in RNA Processing Suppression of apoptosis Phosphorylated BMAL1:CLOCK (ARNTL:CLOCK) activates expression of core clock genes Activation of NOXA and translocation to mitochondria Activation of PUMA and translocation to mitochondria Pre-NOTCH Transcription and Translation Formation of Senescence-Associated Heterochromatin Foci (SAHF) DNA Damage/Telomere Stress Induced Senescence Autodegradation of the E3 ubiquitin ligase COP1 Association of TriC/CCT with target proteins during biosynthesis Pyroptosis TP53 Regulates Metabolic Genes Ub-specific processing proteases Ovarian tumor domain proteases Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks Interleukin-4 and Interleukin-13 signaling TP53 Regulates Transcription of DNA Repair Genes TP53 Regulates Transcription of Genes Involved in Cytochrome C Release TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain TP53 Regulates Transcription of Caspase Activators and Caspases TP53 Regulates Transcription of Death Receptors and Ligands TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest TP53 regulates transcription of additional cell cycle genes whose exact role in the p53 pathway remain uncertain TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest Regulation of TP53 Expression Regulation of TP53 Activity through Phosphorylation Regulation of TP53 Degradation Regulation of TP53 Activity through Acetylation Regulation of TP53 Activity through Association with Co-factors Regulation of TP53 Activity through Methylation mRNA Splicing - Major Pathway Dengue Virus-Host Interactions PIP3 activates AKT signaling Constitutive Signaling by Aberrant PI3K in Cancer Sema4D mediated inhibition of cell attachment and migration RAF/MAP kinase cascade MET Receptor Activation Negative regulation of MET activity PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling MET activates RAS signaling MET activates PI3K/AKT signaling MET activates PTPN11 MET activates PTK2 signaling InlB-mediated entry of Listeria monocytogenes into host cell MET interacts with TNS proteins MET activates RAP1 and RAC1 MET receptor recycling MET activates STAT3 MECP2 regulates neuronal receptors and channels Drug-mediated inhibition of MET activation ER Quality Control Compartment (ERQC)

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2Fase 243
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·Pré-clínico26
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Publicações mais relevantes

🥉Melhor nível de evidência: Relato de caso
Timeline de publicações
29.695 papers (10 anos)

Mostrando amostra de 200 publicações de um total de 29.695

#1

ODF3B Promotes the Progression of Clear Cell Renal Cell Carcinoma via the JAK/STAT Signaling Pathway.

Medical science monitor : international medical journal of experimental and clinical research2026 Mar 25

BACKGROUND Clear cell renal cell carcinoma (ccRCC) is the most common renal malignancy, often associated with poor prognosis due to metastasis and treatment resistance. The Janus kinase/signal transducer and activator of transcription (JAK/STAT) pathway is a major oncogenic driver in ccRCC, but its upstream regulators remain unclear. Outer dense fiber of sperm tails 3B (ODF3B), initially identified in sperm flagella, shows aberrant expression in a subset of human malignancies, and emerging transcriptomic data suggest notable dysregulation of ODF3B in ccRCC, although its functional role in this tumor type remains unknown. MATERIAL AND METHODS ODF3B expression was analyzed using data from The Cancer Genome Atlas (TCGA) and validated in ccRCC cell lines. Prognostic significance was evaluated through clinicopathological and survival analyses. Functional assays, including Cell Counting Kit 8, colony formation, wound healing, Transwell assay, and flow cytometry, were performed after ODF3B knockdown in 786-O and OSRC-2 cells. Pathway enrichment analyses and Western blotting were used to explore mechanisms, and rescue experiments were conducted with the STAT3 agonist Colivelin TFA. RESULTS ODF3B was markedly upregulated in ccRCC tissues and cells, with high expression correlating with advanced stage, metastasis, and poor survival. ODF3B silencing suppressed proliferation, migration, and invasion while enhancing apoptosis, accompanied by reduced BCL2 and increased cleaved caspase-3. Bioinformatics revealed strong enrichment of JAK/STAT signaling in tumors with high expression of ODF3B. Mechanistically, ODF3B knockdown decreased phosphorylation of JAK1/2/3 and STAT3, whereas STAT3 activation rescued proliferative and anti-apoptotic effects. CONCLUSIONS ODF3B acts as a novel oncogenic driver in ccRCC by activating JAK/STAT signaling. Its overexpression predicts aggressive features and poor prognosis, highlighting ODF3B as a potential therapeutic target.

#2

MAGI3 deficiency unleashes β-catenin conformational change to drive metastatic progression and mTOR inhibitor resistance in ccRCC.

Cell death &amp; disease2026 Mar 24

Metastatic clear cell renal cell carcinoma (ccRCC) remains lethal due to therapy resistance, and while dysregulated Wnt/β-catenin signaling drives progression, its post-translational regulation is poorly understood. Through multi-omics analysis of TCGA/GEO datasets, we identified MAGI3 as a key metastasis suppressor in ccRCC. Functional validation revealed that MAGI3 loss enhances invasion, migration and metastatic potential in vitro and in vivo. Mechanistically, MAGI3 binds β-catenin's C-terminus via PDZ domains, disrupting intramolecular N-terminus-ARM domain interactions to expose phosphorylation sites, thereby enabling GSK-3β-mediated β-catenin phosphorylation and ubiquitin-dependent degradation. Critically, low MAGI3 hyperactivates β-catenin and drives mTOR inhibitor resistance. Combining Everolimus with the Wnt inhibitor XAV-939 slashed viability and invasion in resistant cells. Clinically, patients whose tumors exhibited high MAGI3 and low β-catenin expression demonstrated significantly improved response to Everolimus therapy. In conclusion, MAGI3 is a critical gatekeeper of β-catenin destruction in ccRCC. Its loss defines a metastatic, therapy-resistant subtype targetable by dual mTOR/Wnt blockade. Therefore, MAGI3 expression may stratify patients for personalized therapy.

#3

DR5/WDR12 balances p65 stability promoting sunitinib resistance in renal cell carcinoma.

Cell death and differentiation2026 Mar 23

Although the use of tyrosine kinase inhibitors (TKIs), such as sunitinib, has led to impressive advancements in the treatment of clear cell renal cell carcinoma (ccRCC), primary or acquired resistance to sunitinib remains elusive. Here, we report that death receptor 5 (DR5) is upregulated in ccRCC tissues and sunitinib-resistant cells, and is associated with poor outcomes and sunitinib resistance. Gain- and loss-of-function experiments revealed that DR5 promotes sunitinib resistance both in vitro and in vivo. Mechanistically, DR5 enhances the activation of NF-κB signalling by reducing the ubiquitin-mediated proteasomal degradation of p65 via competitive binding to the CUL4B-DDB1 E3 ligase complex linker protein WDR12, leading to the transcriptional upregulation of DR5 and BCL2. The positive feedback loop between DR5 and p65 contributes to the upregulation of BCL2 expression, which in turn modulates sunitinib resistance in ccRCC. Notably, targeting the DR5/NF-κB/BCL2 axis sensitizes ccRCC cells to sunitinib both in vitro and in vivo. Clinically, ccRCC patients with high DR5 expression show decreased responsiveness to TKI-based therapy. Collectively, these results highlight the importance of the positive feedback loop involving the DR5/NF-κB axis in sunitinib resistance and provide an effective therapeutic strategy for overcoming resistance.

#4

TRIM21-Mediated ubiquitination of FBL suppresses PI3K/AKT signaling and tumor progression in clear cell renal cell carcinoma.

Cellular and molecular life sciences : CMLS2026 Mar 21

Clear cell renal cell carcinoma (ccRCC) frequently exhibits transcriptional reprogramming driven by oncogenic C-Myc. Fibrillarin (FBL), a nucleolar C-Myc target, is markedly upregulated in ccRCC, correlating with poor prognosis and essential for tumor cell survival. Integrated single-cell RNA sequencing, bulk transcriptomics, and proteomics were used to identify FBL as a key target. Functional assays, immunoprecipitation-mass spectrometry, and molecular docking were performed to investigate FBL's oncogenic mechanisms and interaction with TRIM21. FBL promotes ccRCC cell proliferation, migration, and tumor growth via PI3K/AKT pathway activation. TRIM21 was identified as a novel FBL-binding E3 ubiquitin ligase that catalyzes K48-linked polyubiquitination of FBL at lysine 292, accelerating its proteasomal degradation. TRIM21 overexpression reduces FBL levels, inhibits PI3K/AKT signaling, and reverses FBL-induced oncogenic phenotypes. TRIM21 is downregulated in ccRCC tissues and associated with unfavorable prognosis. The TRIM21-FBL axis regulates ccRCC progression by modulating PI3K/AKT signaling, providing mechanistic insight and potential therapeutic targets for ribosome biogenesis and oncogenic signaling.

#5

ZBED6-IGF2-PIK3C3 autophagy axis drives ccRCC progression: A multi-omics integration study.

iScience2026 Mar 20

Autophagy supports clear cell renal cell carcinoma (ccRCC) progression, yet its upstream regulatory mechanisms remain to be fully defined. Integrating bulk, single-cell, and spatial transcriptomics, we identify a regulatory axis wherein the transcription factor ZBED6 activates the expression of the autophagy-initiating kinase PIK3C3 via the repression of IGF2, thereby driving pro-tumorigenic autophagy. Spatial analysis confirms the co-localization of ZBED6 and PIK3C3 in tumor tissues. Using genes associated with this axis, we develop a six-gene prognostic signature that stratifies patients with distinct survival outcomes and differential responses to immunotherapy and targeted therapy. Functional assays show that ZBED6 promotes ccRCC cell proliferation, migration, and invasion. This work elucidates a pathway governing autophagy in ccRCC and provides a framework for prognostic assessment and precision therapy.

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2026

Intra-arterial infusion of bevacizumab for the treatment of peritoneal metastatic high-grade renal cell carcinoma: a case report.

Frontiers in immunology
2026

Whole-body magnetic resonance imaging for cancer screening in asymptomatic adults: a multicenter study.

European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP)
2026

ODF3B Promotes the Progression of Clear Cell Renal Cell Carcinoma via the JAK/STAT Signaling Pathway.

Medical science monitor : international medical journal of experimental and clinical research
2026

Preoperative assessment of split renal function in patients with renal cell carcinoma by APTw driven multiparameter MRI.

BMC medical imaging
2026

MAGI3 deficiency unleashes β-catenin conformational change to drive metastatic progression and mTOR inhibitor resistance in ccRCC.

Cell death &amp; disease
2026

Genome-wide CRISPR screen identifies a cytokine-enhancer circuit driving HIF-2α activation in renal cancer.

The Journal of clinical investigation
2026

Unclear territory: navigating metastatic nonclear cell renal cell carcinoma.

Current opinion in oncology
2026

Short and Long Non-Coding RNAs in Renal Cell Carcinoma.

Non-coding RNA
2026

Pulmonary Metastases From Undiagnosed Prostate Cancer Mimicking Late Recurrence of Renal Cell Carcinoma: Diagnosis Confirmed by Thoracoscopic Biopsy.

Cureus
2026

Epigenetic activation of VEGFA by SMARCD1 mediates tumor progression and bevacizumab resistance in clear cell renal cell carcinoma.

BMC cancer
2026

SETD2 methyltransferase activity promotes correct transcription initiation and termination.

EMBO reports
2026

DR5/WDR12 balances p65 stability promoting sunitinib resistance in renal cell carcinoma.

Cell death and differentiation
2026

Patient-derived organoids in renal cell carcinoma: A review of methodologies and applications.

Urologic oncology
2026

Society for Immunotherapy of Cancer (SITC) clinical practice guideline on immunotherapy for the treatment of renal cell carcinoma, version 3.0.

Journal for immunotherapy of cancer
2026

The role of spinal stereotactic radiosurgery in the treatment of renal cell carcinoma spinal metastases.

Journal of neurosurgery. Spine
2026

Rare renal tumor: a case report of collecting duct carcinoma and literature review.

Frontiers in oncology
2026

A Life-Threatening Metastasis of Renal Cell Carcinoma: An Endotracheal Metastasis.

Cureus
2026

Identification of risk factors for the development and prognosis of bone metastases in renal cell carcinoma: development and validation of a predictive model.

American journal of cancer research
2026

Metastatic renal cell carcinoma to the thyroid gland with tracheal invasion: A case report.

Radiology case reports
2026

Makorin Ring Finger Protein 1 Inhibits Cell Proliferation in Renal Angiomyolipoma via the ERK/MAPK Signaling Pathway.

Kidney diseases (Basel, Switzerland)
2026

Intraventricular metastasis: A systematic review of patient demographics, clinical characteristics, and outcomes.

Neuro-Chirurgie
2026

SLAMF1 at the crossroads of immunity and disease: Biology, pathology, and therapeutic opportunities.

Cytokine
2026

An interpretable machine learning model based on habitat radiomics combined with deep learning for predicting the WHO/ISUP grade of patients with clear cell renal cell carcinoma.

BMC medical imaging
2026

Monogenic and Polygenic Risk for Kidney Cancer in Two Large Biobanks.

European urology oncology
2026

Endothelial SMAD1-MCAM axis facilitates sunitinib resistance and progression of clear cell renal cell carcinoma via LAMB1-ITGB1 signaling.

Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy
2026

Multi-omics profiling identifies ectopic olfactory receptors as putative drivers of tumor progression and prognostic indicators in clear cell renal cell carcinoma.

Clinical and experimental medicine
2026

TRIM21-Mediated ubiquitination of FBL suppresses PI3K/AKT signaling and tumor progression in clear cell renal cell carcinoma.

Cellular and molecular life sciences : CMLS
2026

PARTIAL: study protocol for a clinical and cost-effectiveness of complex PARTIAL vs radical nephrectomy for clinically localised renal cell carcinoma randomised trial.

Trials
2026

Hemoperitoneum detected by peritoneal dialysis as presenting symptom of cytomegalovirus-associated colitis: a case report.

BMC nephrology
2026

Bridging urology and palliative care: a narrative review of current practice and evolving priorities.

Current opinion in urology
2026

Renal cell carcinoma presenting with orbital metastasis as the initial symptom: A case report.

Medicine
2026

Recurrent Mental Cutaneous Metastases Secondary to Bilateral Renal Cell Carcinoma.

Cureus
2026

RAB24 maps comprehensive clinical landscapes and mediates tumor malignant progression under the epigenetic regulation of miR-30b-3p and MMP11 in clear cell renal cell carcinoma.

Genes &amp; diseases
2026

ZBED6-IGF2-PIK3C3 autophagy axis drives ccRCC progression: A multi-omics integration study.

iScience
2026

A prospective head-to-head comparison of 18F-NYM005 PET/CT and 18F-FDG PET/CT in diagnosing renal cell carcinoma.

European journal of nuclear medicine and molecular imaging
2026

FUT8 reprograms glycolytic metabolism to promote PKM2 lactylation and drive clear cell renal cell carcinoma progression.

Cell death discovery
2026

ZDHHC9 palmitoylates LAMTOR1 to promote renal cell carcinoma malignant progression.

Cell death &amp; disease
2026

A Systematic Review and Meta-Analysis of the Significance of Diabetes on Kidney Cancer Outcomes and the Role of Metformin.

Clinical genitourinary cancer
2026

[The effect of preoperative inflammatory indicators on the prognosis of patients with T1a renal cell carcinoma undergoing surgery and the construction of a predictive model].

Zhonghua yi xue za zhi
2026

Comparison of clinical characteristics between patients with single mutation and co-mutation in hereditary renal cancer: a retrospective analysis of 115 patients with von Hippel-Lindau syndrome.

Journal of medical genetics
2026

Clinical characteristics and follow-up of 77 patients with pathogenic fumarate hydratase variants.

BJU international
2026

Renal Clear Cell Carcinoma Discovered Following Pyothorax: A Case Report.

Cureus
2026

Late-Onset Normotensive Thrombotic Microangiopathy and Pyoderma Gangrenosum Following Nine Years of Sunitinib Therapy: A Case Report.

Kidney medicine
2026

Ultra-late pancreatic metastases from renal cell carcinoma after nephrectomy: two case reports and a literature review.

Journal of surgical case reports
2026

Renal sinus leiomyoma mimicking papillary renal cell carcinoma: A case report.

Radiology case reports
2026

Development of Celiac Disease After Immunotherapy: A Case Series.

Gastro hep advances
2026

TAOK3 promotes ccRCC progression by phosphorylating ASAP2.

Biochimica et biophysica acta. Molecular basis of disease
2026

Pan-cancer multi-omics profiling of gasdermins identifies GSDMD as an immune-related prognostic biomarker in kidney renal clear cell carcinoma.

Discover oncology
2026

Combinatorial immunotherapy drives exhaustion in tumor antigen-specific CD8+ T cells within the mouse renal tumor microenvironment.

Journal of immunology (Baltimore, Md. : 1950)
2026

Surgery and toceranib for renal cell carcinoma with caval thrombus in a dog.

The Canadian veterinary journal = La revue veterinaire canadienne
2026

Correlation of mRENAL score with clinical outcomes after CT-guided renal cell carcinoma cryoablation: A retrospective observational study.

Qatar medical journal
2026

Increased expression of CD36 and CD163 in clear cell renal cell carcinoma suggests an association between lipid transport and an "M2-like" macrophage phenotype.

Frontiers in immunology
2026

Survivorship after Kidney Cancer in Children, Adolescents and Young Adults- What is Causing Death and When?

Urology
2026

Oxalate induces proliferation and mitochondrial metabolism in select clear cell renal cell carcinoma cell lines.

BMC cancer
2026

Percutaneous Cryoablation of Clinical T1b Renal Tumors: A Tertiary Cancer Center Experience.

Cardiovascular and interventional radiology
2026

Initial and Repeat Metastasis-Directed Therapy in Systemic Therapy-Naïve Oligometastatic Renal Cell Carcinoma: Oncologic Outcomes and Risk-Based Stratification.

Annals of surgical oncology
2026

USP20 governs tyrosine kinase inhibitors resistance through ferroptosis evasion by targeting GPX4 in cancers.

Redox biology
2026

[Cryoablation for Renal Cell Carcinoma: Update on an Established Ablative Technique].

Aktuelle Urologie
2026

Radiotherapy Utilization Patterns Among Patients With Metastatic Renal Cell Carcinoma of the Spine: A National Claims Database Study.

American journal of clinical oncology
2026

The Cyclin C-CDK8/19 Mediator kinase module controls PRCC-TFE3 driven senescence in renal epithelium and tumorigenesis in TFE3-RCC.

Neoplasia (New York, N.Y.)
2026

A Minimum 3-Year Follow-Up of Nivolumab-Plus-Ipilimumab in Japanese Patients With Advanced or Metastatic Renal Cell Carcinoma: A Final Analysis of the J-ENCORE Study.

International journal of urology : official journal of the Japanese Urological Association
2025

Does Tumor Grade Have any Prognostic Significance in Chromophobe Renal Cell Carcinoma: A Clinicopathological Study.

Journal of cancer &amp; allied specialties
2026

A Survey of Oncologists' Perceptions and Opinions Regarding Brain Imaging in Metastatic Renal Cell Carcinoma Within the UK.

Cureus
2026

Protocol for constructing an orthotopic mouse model of metastatic renal cell carcinoma.

STAR protocols
2026

Adrenocortical Carcinoma as a Manifestation of Birt-Hogg Dubé Syndrome.

Endocrine-related cancer
2026

Recurrent spontaneous pneumothorax and surgical management in Birt-Hogg-Dubé syndrome: a case report.

International journal of surgery case reports
2026

A case report of the world's biggest renal cell carcinoma successfully removed.

International journal of surgery case reports
2026

New-onset renal impairment following radical nephrectomy for renal cell carcinoma: a retrospective cohort study of clinical, intraoperative, and postoperative risk factors.

Therapeutic advances in urology
2026

IL20RB promotes proliferation and migration in clear cell renal cell carcinoma and is associated with immune infiltration.

PeerJ
2026

Epithelial-mesenchymal transition and sunitinib resistance in renal cell carcinoma: mechanisms and therapeutic strategies.

Frontiers in pharmacology
2026

Large sarcomatoid chromophobe renal cell carcinoma with tumor thrombus extending into the inferior vena cava: a case report on the challenges and lessons from a fatal outcome.

Annals of translational medicine
2026

FloSeal® for Parenchymal Hemostasis in Robot-Assisted Partial Nephrectomy: Technical Description and a Report of Two Cases.

Cureus
2026

Surgical Resection of Abdominal Solid Organ Tumors With Inferior Vena Cava Extension: A Single-Center Experience With Long-Term Follow-Up.

Cureus
2026

Nutrient intake and renal cancer: molecular pathways and mechanistic insights into the protective role of dietary components.

Frontiers in nutrition
2026

Safety, Efficacy, and Intermediate‑Term Outcomes of CT‑Guided Cryoablation of T1 Renal Cell Carcinoma: A Retrospective Single‑Center Study.

Journal of the Belgian Society of Radiology
2026

Taraxasterol Suppresses Renal Cell Carcinoma Progression by Modulating Cell Cycle Progression and Apoptosis.

Anti-cancer agents in medicinal chemistry
2026

Predicting aggressiveness of clear cell renal cell carcinoma via mri using artificial intelligence: implications for surgical planning in a retrospective multicenter study.

Scientific reports
2026

Sterotactic ablative radiotherapy vs. thermal ablation of localized renal cell carcinoma: Is there a preferred second-line management option?

Urologic oncology
2026

Proton beam therapy versus photon therapy for multiple malignancies: An umbrella systematic review and meta-analysis.

Critical reviews in oncology/hematology
2026

Serum Chemokines CCL3 and CCL7 as Complementary Diagnostic Biomarkers Across Tumor Grades in Clear Cell Renal Cell Carcinoma.

International journal of molecular sciences
2026

Updates on Clinical Trials and Molecular Characteristics of Locally Advanced and Oligometastatic Renal Cell Carcinoma.

International journal of molecular sciences
2026

Opportunities and Challenges of Visual Large Language Models in Imaging Diagnostics: Lessons from Brain Metastasis Detection in Clinical MRI.

Diagnostics (Basel, Switzerland)
2026

VEGF-TKI Outcomes in Metastatic Renal Cell Carcinoma According to Prior Immune Checkpoint Inhibitor or VEGF-TKI: A Scoping Review and Exploratory Analysis.

Cancers
2026

Angiogenesis-Informed Preoperative CT Radiogenomics Predicts Overall Survival in Clear Cell Renal Cell Carcinoma: Development and External Validation.

Cancers
2026

Impact of Peri-Immunotherapy Antibiotic Exposure on Survival Outcomes in Metastatic Renal Cell Carcinoma: A Real-World IMDC Risk-Stratified Analysis.

Journal of clinical medicine
2026

DPP9 inhibition boosts antitumor immunity by disrupting BRISC-mediated PD-L1 expression in clear cell renal cell carcinoma.

Cell death and differentiation
2026

Liquid-Based Cytologic Features of a Thyroid TFE3-Rearranged PEComa-Like Neoplasm: A Case Report.

Diagnostic cytopathology
2026

The Staging of High-risk And non-metastatic Renal cell carcinoma Preoperatively (SHARP) Model predicts pathologic T3 stage for neoadjuvant clinical trial enrollment.

Urology
2026

Multidisciplinary therapy managements in endometrial and renal cancer patients treated with pembrolizumab and lenvatinib: a virtuous circle between oncologists and organ specialists.

Critical reviews in oncology/hematology
2026

Targeting pH regulation in cancer: combined mild alkaline treatment and NHE1 inhibition as a potential therapy for clear cell renal cell carcinoma.

Molecular and cellular biochemistry
2026

A new cuproptosis-associated lncRNA signature predicts the prognosis of clear cell renal cell carcinoma patients.

Discover oncology
2026

Stereotactic ablative radiotherapy: an effective alternative for pancreatic metastases originating from renal cell carcinoma-experience from two European institutions.

Clinical &amp; experimental metastasis
2026

Application of carbonic anhydrase IX-targeted radiopharmaceuticals in the diagnosis and treatment of clear cell renal cell carcinoma (Review).

Oncology letters
2026

Machine learning-derived AS and AIS scores leverage BCAA metabolism and IL4I1 activity for prognosis and tailored therapy in ccRCC.

Frontiers in cell and developmental biology
2026

Functional and Survival Outcomes of Partial Versus Radical Nephrectomy in Renal Cell Carcinoma Patients With Pre-Existing Chronic Kidney Disease: A Real-World Study.

World journal of oncology
2026

Tertiary lymphoid structures in genitourinary cancers: a comprehensive review.

Frontiers in oncology
2026

The prognostic impact of systemic inflammation and nutritional indicators on targeted therapy for renal cell carcinoma: a systematic review and meta-analysis.

Frontiers in nutrition
2026

Elevated DOCK4 expression correlates with favorable prognosis and immune infiltration in clear cell renal cell carcinoma.

Annals of medicine
2026

Impact of Perioperative Proton Pump Inhibitors on Renal Cancer Progression. A Retrospective Study.

Cancer medicine
2026

Pattern and Clinical Significance of CA19-9 Expression in Human Cancer: A Tissue Microarray Study on 14,966 Tumors.

Cancer medicine
2026

Feasibility of Spectral Computed Tomography Color Overlay to Augment Tumor Visibility for Renal Cryoablation.

Cardiovascular and interventional radiology
2026

Impact of high relative dose intensity on effectiveness and treatment continuity of IO-TKI therapy in Japanese advanced renal cell carcinoma.

Scientific reports
2026

VHL synthetic lethality screens uncover CBF-β as a negative regulator of STING.

Nature communications
2026

Value of High Frame Rate Contrast-enhanced Ultrasound in Evaluating Vascular Morphology of Renal Cell Carcinoma.

Current medical imaging
2026

[rare subtype of kidney cancer - Pigmented microcystic chromophobe carcinoma].

Magyar onkologia
2026

Comprehensive immunohistochemical and molecular characterization of paratesticular clear cell papillary cystadenomas: A multi-institutional study of 14 cases.

Annals of diagnostic pathology
2026

A lactylation-related gene signature predicts prognosis and immunotherapy response in clear cell renal cell carcinoma based on machine learning and multi-omics analysis.

Discover oncology
2026

Comparative outcomes and costs of robotic assisted, laparoscopic, and open partial nephrectomy: a contemporary analysis of national inpatient sample data.

World journal of urology
2026

Anastomosing hemangioma of the renal pelvis: The first case report from Vietnam.

Urology case reports
2026

Symptomatic renal tumor in mid-pregnancy managed with nephrectomy and term vaginal delivery: a case report and literature review.

International journal of surgery case reports
2026

Renal schwannoma appears on imaging as renal cell carcinoma: a case report.

Journal of medical case reports
2026

Ultrasound-assisted diagnosis and ultrasound-guided radiofrequency ablation of renal cell carcinoma in a patient with autosomal dominant polycystic kidney disease: a case report with two-year follow-up.

BMC nephrology
2026

Baseline and three-month De Ritis ratio and gamma-glutamyltransferase as prognostic biomarkers in metastatic renal cell carcinoma treated with targeted therapy.

Scientific reports
2026

Gamma-aminobutyric acid transaminase mediates tumor suppression in renal cell carcinoma through the cGAS-STING-interferon-β axis.

Scientific reports
2026

Long non-coding RNA PSMB8-AS1 as a potential biomarker for postoperative recurrence in patients with Fuhrman grades 1-3 clear cell renal cell carcinoma.

PloS one
2026

Multi-omics integration constructs a senescence-based prognostic model and identifies EIF4EBP1 as a therapeutic target in clear cell renal cell carcinoma.

Discover oncology
2026

Barriers to Health Care Access and Use among Racial and Ethnic Minorities with Renal Cell Carcinoma.

Urology practice
2026

In vivo self-assembled siRNAs targeting VEGFR2 and mTOR for renal cell carcinoma treatment.

Asian journal of pharmaceutical sciences
2026

Why Does DNA Methylation Accumulate at CpG Loci?: Sequential Analysis of Cdkn2a/p16Ink4a Gene Methylation in a Rat Renal Tumor Model.

Acta histochemica et cytochemica
2026

Current research on the HIF-2α-EPO-Hb axis in hypoxic environments: from molecular mechanisms to clinical.

Frontiers in medicine
2026

One size does not fit all: rethinking IO-TKI use in favorable-risk metastatic ccRCC.

Frontiers in oncology
2026

Combined assessment of ERO1A expression and CD163+ tumor-associated macrophage infiltration is superior to traditional assessment methods in predicting clear cell renal cell carcinoma prognosis.

Frontiers in oncology
2026

Anticoagulant outcomes in managing tumor thrombus: a systematic review.

Frontiers in oncology
2026

Identification of prognostic factors for postoperative recurrence-free survival in T2-stage renal cell carcinoma: a retrospective cohort study.

Translational andrology and urology
2026

First report of transumbilical robotic-assisted single-port laparoscopic partial nephrectomy using a domestic Shurui® robotic system: a report of two cases.

Translational andrology and urology
2026

USP10 regulates HIF2α stability by deubiquitinating HIF2α regardless of VHL status in kidney cancer.

Translational andrology and urology
2026

Development and validation of a risk classification integrating the location index to predict renal function after robotic partial nephrectomy.

Scientific reports
2026

Baseline serum folic acid as a prognostic biomarker in metastatic renal cell carcinoma treated with targeted therapy.

Discover oncology
2026

HIF-2α Inhibitor Combinations Knock Back Kidney Cancer in Two Trials.

Cancer discovery
2026

Transcriptomic profiling of clear cell renal cell carcinoma reveals age-dependent molecular signatures and clinical stratification patterns.

PloS one
2026

Noninvasive Differentiation of Indolent from Aggressive Renal Neoplasms with MR Fingerprinting Combined with Diffusion/Perfusion MRI.

Radiology
2026

Linezolid-induced Posterior Reversible Encephalopathy Syndrome: A Case Report and Review of the Literature.

Clinical neuropharmacology
2026

MicroRNA prognostic markers for immune checkpoint inhibitor success in urologic cancers.

Immunotherapy
2026

A Case of Reactive Lymphoid Hyperplasia That Is Difficult to Differentiate From Renal Cancer With Lymph Node Metastasis.

IJU case reports
2026

Multiphase CT-based deep learning radiomics nomogram models for preoperative WHO/ISUP grading of clear cell renal cell carcinoma: a two-center validation study.

BMC medical imaging
2026

Phosphoethanolamine cytidylyltransferase 2 exerts an anti-tumor role in clear cell renal cell carcinoma by modulating the hippo/YAP1 signaling pathway in a PPP2R1A-dependent manner.

Toxicology and applied pharmacology
2026

Robot-assisted versus open surgery for multiple ipsilateral renal tumors: a multicenter matched cohort study (UroCCR-60).

Journal of robotic surgery
2026

Impact of proton pump inhibitors on immunotherapy is modulated by prior chemotherapy and linked to gut microbiome-immune cell signatures.

Cancer immunology, immunotherapy : CII
2026

Artificial intelligence in urological malignancy diagnosis and prognosis: current status and future prospects.

The Canadian journal of urology
2026

MIRit: an integrative R framework for the identification of impaired miRNA-mRNA regulatory networks in complex diseases.

Bioinformatics advances
2026

GFPT2 drives sunitinib resistance of renal cell carcinoma via enzyme-dependent and -independent manners.

International journal of biological sciences
2026

Renal cell carcinoma incidence and mortality in California: a population-based study of sociodemographic patterns and temporal trends from 1988 through 2019.

Lancet regional health. Americas
2026

Ectopic adrenal nodular hyperplasia mimicking right upper polar renal cell carcinoma: a case report and literature review.

Frontiers in oncology
2026

Patients' knowledge, attitudes, preferences regarding kidney cancer screening, and factors influencing participation intentions: a qualitative study.

Frontiers in oncology
2026

IFI44 Promotes Clear Cell Renal Cell Carcinoma Progression via PRDX1 and Predicts Poor Prognosis.

Research (Washington, D.C.)
2026

Specific in vivo detection of V2R-positive metastatic ccRCC using a toxin-based PET radioligand.

Theranostics
2026

Connective tissue growth factor contributes to resistance to anti-angiogenic therapies in renal cancer.

Theranostics
2026

A Case of Bilateral Renal Cancer in a Dialysis Patient With Enlarged ACDK Treated With Staged Laparoscopic Nephrectomy.

IJU case reports
2026

Determinants of pancreatic tropism in metastatic renal cell carcinoma.

JCI insight
2026

Clear Cell Papillary Renal Cell Tumor Revisited: Comparison of Histologic and Immunohistochemical Profiles in Relation to VHL Allelic Status.

The American journal of surgical pathology
2026

Immuno-molecular features and therapeutic implications of brain metastases in clear cell renal cell carcinoma patients.

Genes and immunity
2026

The oncovascular surgeon in modern surgical oncology: A literature review.

European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology
2026

Survival outcomes after surgical treatment for non-clear cell renal cell carcinoma with tumor thrombus extension: a population-based cohort study.

World journal of urology
2026

Sarcomatoid Renal Cell Carcinoma: Biological Features and Therapeutic Implications-A Narrative Review.

Current urology reports
2026

DNA methyltransferase inhibition is a therapeutic vulnerability in VHL-deficient renal cell carcinoma cells.

Experimental &amp; molecular medicine
2026

Node Positive Resected Renal Cell Carcinoma Portends a Poor Prognosis: Results From the Canadian Kidney Cancer Collaboration.

Clinical genitourinary cancer
2026

Inhibitory effects and molecular mechanisms of Aristolochic acids on human and rat placental 3β-hydroxysteroid dehydrogenases.

Journal of ethnopharmacology
2026

Real-World Outcomes in Advanced Clear Cell Renal Cell Carcinoma: A Retrospective Analysis Comparing New Zealand and Australian Cohorts.

JCO global oncology
2026

Multi-omics analysis suggests ZDHHC18 as a potential risk factor for clear cell renal cell carcinoma linked to myeloid DC morphology.

Discover oncology
2026

ALK-Rearranged Renal Cell Carcinoma: Morphologic Spectrum and Genomic Landscape From a Multi-Institutional Cohort of 16 Cases.

The American journal of surgical pathology
2026

Emerging role of functional imaging in renal cell carcinoma: from morphology to molecular phenotyping with PET/computed tomography.

Current opinion in oncology
2026

Reliable Detection of SGLT2 Protein by Knockout-Based Antibody Characterization.

Hypertension (Dallas, Tex. : 1979)
2026

Case Report: A patient with metastatic fumarate hydratase-deficient renal cell carcinoma associated with leiomyomatosis: real-world clinical insights on systemic therapy and liver-directed SBRT.

Frontiers in oncology
2026

Study on the prediction of postoperative metastasis in renal cancer using perirenal fat CT radiomics combined with clinical features.

Frontiers in oncology
2026

Impact of bone-targeting agents on the clinical outcomes in patients with metastatic renal cell carcinoma treated with nivolumab: a sub-analysis of the Meet-URO 15 study.

Frontiers in oncology
2026

Clear cell renal cell carcinoma combined with intravascular large B-cell lymphoma: a case report and review of the literature.

Frontiers in oncology
2026

CLINICAL CASE OF COMPLEX RADICAL TREATMENT OF METASTATIC PROGRESSION TO RARE SITE OF PRIMARY ORGAN CONFINED CHROMOPHOBE RENAL CELL CARCINOMA TREATED WITH LAPAROSCOPIC PARTIAL NEPHRECTOMY.

Experimental oncology
2026

Gut microbiota modulation of epigenetic target EHMT2: Lacticaseibacillus rhamnosus Fb7-311 regulated renal cell carcinoma apoptosis and metastasis.

Experimental &amp; molecular medicine
2026

Pellino1-mTOR/S6K1 signaling axis is a key pathogenesis for the development of polycystic kidney disease.

Cell death &amp; disease
2026

Nivolumab plus ipilimumab versus sunitinib for first-line treatment of advanced renal cell carcinoma: final analysis of efficacy and safety from the phase III CheckMate 214 trial.

Annals of oncology : official journal of the European Society for Medical Oncology
2026

Outcomes after Pancreatic Resections for Secondary Tumours in the Pancreas: A Single Centre Experience.

Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract
2026

Clinical, pathologic, and molecular profiles of sarcomatoid and rhabdoid differentiated clear cell renal cell carcinoma: A series of 21 tumors.

Human pathology
2026

ICG fluorescence imaging in sentinel lymph node identification: toward a standardized protocol in paediatric renal tumour surgery.

Pediatric surgery international
2026

Citronellol potentiates sunitinib efficacy in renal cell carcinoma by targeting JAK2/STAT3 signaling pathway.

Naunyn-Schmiedeberg's archives of pharmacology
2026

Nitroimidazole-Containing [68Ga]Ga-IPM-N001 as a New CAIX-Targeting Radionuclide Tracer.

Journal of medicinal chemistry
2026

Unraveling the role of LINC02657 in clear cell renal cell carcinoma: insights into tumor aggression, immune modulation, and treatment response.

Frontiers in immunology
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HIF2 drives PTHrP-mediated cancer cachexia.

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Activation of the PI3K/AKT pathway by EDIL3 induces EMT and promotes tumor progression in clear cell renal cell carcinoma.

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Immunohistochemical expression of GPNMB in TFEB-rearranged and TFEB-amplified renal cell carcinomas.

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Influence of body composition on the efficacy of nivolumab plus ipilimumab for metastatic clear cell renal cell carcinoma.

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Modified clear cell likelihood score and a new CAT score in the assessment of indeterminate small renal masses.

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Ver todos os 35.568 no EuropePMC

Associações

Organizações que acompanham esta doença — pra ter apoio e orientação

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Doença com base genética

Um médico geneticista pode ajudar no diagnóstico de Carcinoma de células renais e no aconselhamento genético da família.

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Conselhos e sociedades

Doenças relacionadas

Doenças com sintomas parecidos — ajudam quem ainda está buscando diagnóstico

Perguntas frequentes

O que as famílias mais perguntam sobre esta doença — cada resposta com a fonte de onde saiu

Respostas geradas por IA a partir das fontes citadas

É um tumor maligno que se origina nas células epiteliais glandulares do rim, conhecido popularmente como câncer de rim. A sua prevalência é estimada em 1 a 5 pessoas a cada 10.000 e seu início habitual ocorre na idade adulta.

Referências

Fontes citadas no texto, publicações do grafo e bases de dados usadas neste verbete

10 publicações do grafo RarasNet (PubMed) · 7 bases de dados. Títulos, periódicos e PMIDs vêm direto da fonte, sem intermediação de IA.

  1. ODF3B Promotes the Progression of Clear Cell Renal Cell Carcinoma via the JAK/STAT Signaling Pathway.
    Medical science monitor : international medical journal of experimental and clinical research2026PMID 41877380
  2. ORPHA:217071
    Orphanet
  3. GARD:13215
    GARD (NIH)
  4. Q1164529
    Wikidata

Dados compilados pelo RarasNet a partir de fontes abertas (Orphanet, OMIM, MONDO, PubMed/EuropePMC, ClinicalTrials.gov, DATASUS, PCDT/MS). Este conteúdo é informativo e não substitui avaliação médica.

Citar este verbete

Raras. (s.d.). Carcinoma de células renais. Em Raras — Enciclopédia de Doenças Raras do Brasil. https://raras.org/doenca/carcinoma-de-celulas-renais

Formato APA. Conteúdo sob CC BY 4.0 — reuso livre com atribuição.

Conteúdo mantido por Agente Raras · Médicos e pesquisadores podem colaborar

Carcinoma de células renais
Compêndio · Raras BR

Carcinoma de células renais

ORPHA:217071 · MONDO:0005086
Prevalência
1-5 / 10 000
Herança
Not applicable
CID-10
C64 · Neoplasia maligna do rim, exceto pelve renal
CID-11
Ensaios
495 ativos
Início
Adult
Prevalência
42.0 (Europe)
MedGen
UMLS
C0007134
Repurposing
7 candidatos
axitinib — PDGFR tyrosine kinase receptor inhibitor|VEGFR inhibitor
everolimus — mTOR inhibitor
pazopanib — KIT inhibitor|PDGFR tyrosine kinase receptor inhibitor|VEGFR inhibitor
+4 outros
Wikidata
Wikipedia
Papers 10a
Evidência
🥉 Relato de caso

📋 Origem dos dados

Esta página agrega dados de fontes públicas e oficiais. Dados sobre cobertura no SUS (PCDT, CEAF) são verificados ativamente por agente proativo (ver badge no infobox). Demais dados têm atribuição de fonte + data da última sincronização — clique para abrir o original.

Doença rara (ontologia)
fonte: Orphanet
Identificador unificado
fonte: MONDO
Indexação biomédica
fonte: MeSH (NLM)
Dado público estruturado
fonte: Wikidata
Medicamentos aprovados FDA
fonte: FDA OpenFDA
Rara