Por favor, use este identificador para citar o enlazar este ítem: http://hdl.handle.net/10201/52373

Título: BAG3: a new therapeutic target of human cancers?
Fecha de publicación: 2012
Editorial: F. Hernandez y JuanF. Madrid. Universidad de Murcia. Departamento de Biología Celular e Histología.
Cita bibliográfica: Histology and Hispathology, vol. 27, n. 3, 2012
ISSN: 2013-3911
1699-5848
Materias relacionadas: CDU::5 - Ciencias puras y naturales::57 - Biología
Palabras clave: Cancer
Apoptosis
Resumen: Bcl-2-associated athanogene (BAG) family proteins share the BAG domain, which is characterized by their interaction with a variety of partners (heat shock proteins, steroid hormone receptors, Raf-1 and others) and is involved in regulating a number of cellular processes. BAG3, also known as CAIR-1 or Bis, mediates protein delivery to proteasome and modulates apoptosis by interfering with cytochrome c release, apoptosome assembly and other events in the cellular death program. Moreover, it takes part in the processes of cell adhesion and migration. It has been shown that, in human cancer cells, including lymphocytic and myeloblastic leukemic cells, BAG3 sustains cell survival and underlies resistance to chemotherapy, through down-modulation of apoptosis. BAG3 knocking down could enhance the effectiveness of chemotherapy. This review summarizes the physiological and pathological roles of BAG3 in cancer cells and its potential as a therapeutic target of human malignancies.
Autor/es principal/es: Huayuan, Zhu
Peng, Liu
Jianyong, Li
URI: http://hdl.handle.net/10201/52373
Tipo de documento: info:eu-repo/semantics/article
Número páginas / Extensión: 5
Derechos: info:eu-repo/semantics/openAccess
Aparece en las colecciones:Vol.27, nº 3 (2012)

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