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癌症中的突变型p53:积累、功能获得与治疗

Mutant p53 in Cancer: Accumulation, Gain-of-Function, and Therapy.

作者信息

Yue Xuetian, Zhao Yuhan, Xu Yang, Zheng Min, Feng Zhaohui, Hu Wenwei

机构信息

Rutgers Cancer Institute of New Jersey, Rutgers, the State University of New Jersey, New Brunswick, NJ 08903, USA.

Department of Hematology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, China.

出版信息

J Mol Biol. 2017 Jun 2;429(11):1595-1606. doi: 10.1016/j.jmb.2017.03.030. Epub 2017 Apr 6.

Abstract

Tumor suppressor p53 plays a central role in tumor suppression. p53 is the most frequently mutated gene in human cancer, and over half of human cancers contain p53 mutations. Majority of p53 mutations in cancer are missense mutations, leading to the expression of full-length mutant p53 (mutp53) protein. While the critical role of wild-type p53 in tumor suppression has been firmly established, mounting evidence has demonstrated that many tumor-associated mutp53 proteins not only lose the tumor-suppressive function of wild-type p53 but also gain new activities to promote tumorigenesis independently of wild-type p53, termed gain-of-function. Mutant p53 protein often accumulates to very high levels in tumors, contributing to malignant progression. Recently, mutp53 has become an attractive target for cancer therapy. Further understanding of the mechanisms underlying mutp53 protein accumulation and gain-of-function will accelerate the development of targeted therapies for human cancer harboring mutp53. In this review, we summarize the recent advances in the studies on mutp53 protein accumulation and gain-of-function and targeted therapies for mutp53 in human cancer.

摘要

肿瘤抑制因子p53在肿瘤抑制中发挥核心作用。p53是人类癌症中最常发生突变的基因,超过半数的人类癌症含有p53突变。癌症中大多数p53突变是错义突变,导致全长突变型p53(mutp53)蛋白的表达。虽然野生型p53在肿瘤抑制中的关键作用已得到确凿证实,但越来越多的证据表明,许多肿瘤相关的mutp53蛋白不仅丧失了野生型p53的肿瘤抑制功能,还获得了独立于野生型p53促进肿瘤发生的新活性,即功能获得。突变型p53蛋白在肿瘤中常积累到非常高的水平,促进恶性进展。最近,mutp53已成为癌症治疗的一个有吸引力的靶点。进一步了解mutp53蛋白积累和功能获得的潜在机制将加速针对携带mutp53的人类癌症的靶向治疗的发展。在这篇综述中,我们总结了关于mutp53蛋白积累、功能获得以及人类癌症中mutp53靶向治疗研究的最新进展。

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