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p38丝裂原活化蛋白激酶作为肿瘤抑制因子的新作用。

p38 MAP kinase's emerging role as a tumor suppressor.

作者信息

Bulavin Dmitry V, Fornace Albert J

机构信息

Institute of Cellular and Molecular Biology, Singapore.

出版信息

Adv Cancer Res. 2004;92:95-118. doi: 10.1016/S0065-230X(04)92005-2.

Abstract

The p38 proteins are an evolutionally conserved family of mitogen-activated protein kinases (MAPK). Recent studies have led to progress in our understanding the roles of p38 MAPK in regulation of tumorigenesis through key cellular growth-control mechanisms. Along with the previously well-characterized proapoptotic functions, new data highlight the critical contributions of p38 MAPK in the negative regulation of cell cycle progression. This review will focus on the ability of p38 MAPK to positively regulate several tumor suppressor (p53- and Rb-dependent) pathways and to attenuate oncogenic (Cdc25A and Cdc25B phosphatases) signals. The concept of p38 MAPK as a potential tumor suppressor will be developed.

摘要

p38蛋白是丝裂原活化蛋白激酶(MAPK)家族中进化保守的成员。最近的研究使我们在理解p38 MAPK通过关键细胞生长控制机制在肿瘤发生调控中的作用方面取得了进展。除了之前已充分了解的促凋亡功能外,新数据突出了p38 MAPK在细胞周期进程负调控中的关键作用。本综述将聚焦于p38 MAPK正向调控几种肿瘤抑制(依赖p53和Rb)途径以及减弱致癌(Cdc25A和Cdc25B磷酸酶)信号的能力。p38 MAPK作为潜在肿瘤抑制因子的概念将得到深入探讨。

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