Molecular biology of renal cell carcinoma
Clin. transl. oncol. (Print)
; 8(10): 706-710, oct. 2006. ilus, tab
Artigo
em Inglês
| IBECS
| ID: ibc-125317
Biblioteca responsável:
ES1.1
Localização: BNCS
ABSTRACT
Recent developments in molecular biology have lead to an increased understanding of the events involved in renal cell carcinoma (RCC) carcinogenesis. In this field, basic molecular pathways important to oncogenic transformation secondary to Von Hippel-Lindau (VHL) tumor suppression gene inactivation, associated to clear-cell RCC, have been elucidated. Loss of function of VHL results in the high-expression of pro-angiogenic growth factors, such as vascular endothelial growth factor (VEGF) and platelet derived growth factor (PDGF). New therapies against specific targets in RCC have demonstrated significant clinical activity in patients. These therapeutic approaches are based on the VEGF inhibition by using anti-VEGF monoclonal antibodies (bevacizumab) or multi-kinase inhibitors, that also target PDGF and c-kit tyrosine kinases (sorafenib, sunitinib); or by the inhibition of the mammalian target of rapamycin (mTOR) pathway (temsirolimus). This article reviews current knowledge of molecular pathogenesis of inherited and sporadic RCC (AU)
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Coleções:
Bases de dados nacionais
/
Espanha
Base de dados:
IBECS
Assunto principal:
Benzenossulfonatos
/
Carcinoma de Células Renais
/
Transdução de Sinais
/
Inibidores da Angiogênese
/
Anticorpos Monoclonais Humanizados
/
Neoplasias Renais
/
Anticorpos Monoclonais
/
Antineoplásicos
Limite:
Humanos
Idioma:
Inglês
Revista:
Clin. transl. oncol. (Print)
Ano de publicação:
2006
Tipo de documento:
Artigo
Instituição/País de afiliação:
Hospital Clinic/Spain