Cargando…
Involvement of PBRM1 in VHL disease-associated clear cell renal cell carcinoma and its putative relationship with the HIF pathway
Von Hippel-Lindau (VHL) disease is the main cause of inherited clear-cell renal cell carcinoma (ccRCC) and is caused by germline mutations in the VHL tumor suppressor gene. Bi-allelic VHL alterations lead to inactivation of pVHL, which plays a major role by downstream activation of the hypoxia induc...
Autores principales: | Gad, Sophie, Le Teuff, Gwenaël, Nguyen, Baptiste, Verkarre, Virginie, Duchatelle, Veronique, Molinie, Vincent, Posseme, Katia, Grandon, Benjamin, Da Costa, Melanie, Job, Bastien, Meurice, Guillaume, Droin, Nathalie, Mejean, Arnaud, Couve, Sophie, Renaud, Flore, Gardie, Betty, Teh, Bin Tean, Richard, Stephane, Ferlicot, Sophie |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8548775/ https://www.ncbi.nlm.nih.gov/pubmed/34712359 http://dx.doi.org/10.3892/ol.2021.13096 |
Ejemplares similares
-
Integrative analysis of dysregulated microRNAs and mRNAs in multiple recurrent synchronized renal tumors from patients with von Hippel-Lindau disease
por: Gattolliat, Charles-Henry, et al.
Publicado: (2018) -
Trichloroethylene exposure and somatic mutations of the VHL gene in patients with Renal Cell Carcinoma
por: Charbotel, Barbara, et al.
Publicado: (2007) -
Loss of PBRM1 rescues VHL dependent replication stress to promote renal carcinogenesis
por: Espana-Agusti, Judit, et al.
Publicado: (2017) -
The Most Common VHL Point Mutation R167Q in Hereditary VHL Disease Interferes with Cell Plasticity Regulation
por: Buart, Stéphanie, et al.
Publicado: (2021) -
Renal cell tumour characteristics in patients with the Birt-Hogg-Dubé cancer susceptibility syndrome: a retrospective, multicentre study
por: Benusiglio, Patrick R, et al.
Publicado: (2014)