Your browser doesn't support javascript.
loading
Regulation mechanism of Fbxw7-related signaling pathways (Review).
Zhou, Zhenyu; He, Chuanchao; Wang, Jie.
Afiliación
  • Zhou Z; Department of Hepatobiliary Surgery, Sun Yat-sen Memorial Hospital, Sun Yat­sen University, Guangzhou, Guangdong 510120, P.R. China.
  • He C; Department of Hepatobiliary Surgery, Sun Yat-sen Memorial Hospital, Sun Yat­sen University, Guangzhou, Guangdong 510120, P.R. China.
  • Wang J; Department of Hepatobiliary Surgery, Sun Yat-sen Memorial Hospital, Sun Yat­sen University, Guangzhou, Guangdong 510120, P.R. China.
Oncol Rep ; 34(5): 2215-24, 2015 Nov.
Article en En | MEDLINE | ID: mdl-26324296
ABSTRACT
F-box and WD repeat domain-containing 7 (Fbxw7), the substrate-recognition component of SCFFbxw7 complex, is thought to be a tumor suppressor involved in cell growth, proliferation, differentiation and survival. Although an increasing number of ubiquitin substrates of Fbxw7 have been identified, the best characterized substrates are cyclin E and c-Myc. Fbxw7/cyclin E and Fbxw7/c-Myc pathways are tightly regulated by multiple regulators. Fbxw7 has been identified as a tumor suppressor in hepatocellular carcinoma. This review focused on the regulation of Fbxw7/cyclin E and Fbxw7/c-Myc pathways and discussed findings to gain a better understanding of the role of Fbxw7 in hepatocellular carcinoma.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transducción de Señal / Proteínas de Ciclo Celular / Ubiquitina-Proteína Ligasas / Proteínas F-Box Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Oncol Rep Asunto de la revista: NEOPLASIAS Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Transducción de Señal / Proteínas de Ciclo Celular / Ubiquitina-Proteína Ligasas / Proteínas F-Box Tipo de estudio: Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Oncol Rep Asunto de la revista: NEOPLASIAS Año: 2015 Tipo del documento: Article