Medical Proteomics Research Center, KRIBB, Daejeon 305-806; Department of Bio-Analytical Science, University of Science and Technology, Daejeon 305-350, Korea.
BMB Rep. 2014 Mar;47(3):167-72. doi: 10.5483/bmbrep.2014.47.3.261.
Reactivating the p53 pathway in tumors is an important strategy for anticancer therapy. In response to diverse cellular stresses, the tumor suppressor p53 mediates apoptosis in a transcription-independent and transcription-dependent manner. Although extensive studies have focused on the transcription-dependent apoptotic pathway of p53, the transcription-independent apoptotic pathway of p53 has only recently been discovered. Molecular interactions between p53 and Bcl-2 family proteins in the mitochondria play an essential role in the transcription-independent apoptosis of p53. This review describes the structural basis for the transcription-independent apoptotic pathway of p53 and discusses its potential application to anticancer therapy.
激活肿瘤中的 p53 通路是抗癌治疗的一个重要策略。p53 作为肿瘤抑制因子,可通过转录依赖和非依赖两种方式介导细胞凋亡以应对各种细胞应激。尽管大量研究集中于 p53 的转录依赖型凋亡途径,但 p53 的非转录依赖型凋亡途径直到最近才被发现。p53 与线粒体中 Bcl-2 家族蛋白之间的分子相互作用对于 p53 的非转录依赖型凋亡起着至关重要的作用。本综述描述了 p53 非转录依赖型凋亡途径的结构基础,并讨论了其在抗癌治疗中的潜在应用。