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p53介导c-Myc诱导的细胞凋亡。

Mediation of c-Myc-induced apoptosis by p53.

作者信息

Hermeking H, Eick D

机构信息

Institut für Klinische Molekularbiologie und Tumorgenetik Forschungszentrum für Umwelt und Gesundheit, GSF, München, Germany.

出版信息

Science. 1994 Sep 30;265(5181):2091-3. doi: 10.1126/science.8091232.

Abstract

The cellular proto-oncogene c-myc is involved in cell proliferation and transformation but is also implicated in the induction of programmed cell death (apoptosis). The same characteristics have been described for the tumor suppressor gene p53, the most commonly mutated gene in human cancer. In quiescent mouse fibroblasts expressing wild-type p53 protein, activation of c-Myc was found to induce apoptosis and cell cycle reentry, preceded by stabilization of p53. In contrast, in quiescent p53-null fibroblasts, activation of c-Myc induced cell cycle reentry but not apoptosis. These results suggest that p53 mediates apoptosis as a safeguard mechanism to prevent cell proliferation induced by oncogene activation.

摘要

细胞原癌基因c-myc参与细胞增殖和转化,但也与程序性细胞死亡(凋亡)的诱导有关。肿瘤抑制基因p53也具有相同的特性,它是人类癌症中最常发生突变的基因。在表达野生型p53蛋白的静止小鼠成纤维细胞中,发现c-Myc的激活会诱导凋亡和细胞周期重新进入,这之前p53会稳定。相反,在静止的p53基因缺失的成纤维细胞中,c-Myc的激活诱导细胞周期重新进入,但不诱导凋亡。这些结果表明,p53作为一种保护机制介导凋亡,以防止癌基因激活诱导的细胞增殖。

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