Tetramer Formation of Tumor Suppressor Protein p53: Structure, Function, and Applications

被引:88
|
作者
Kamada, Rui [1 ]
Toguchi, Yu [1 ]
Nomura, Takao [2 ]
Imagawa, Toshiaki [1 ]
Sakaguchi, Kazuyasu [1 ]
机构
[1] Hokkaido Univ, Biol Chem Lab, Dept Chem, Fac Sci, Sapporo, Hokkaido 0600810, Japan
[2] Hokkaido Univ, Ctr Res & Educ Drug Discovery, Fac Pharmaceut Sci, Sapporo, Hokkaido 0600812, Japan
关键词
cancer; tumor suppressor; oligomerization; structure; bio-nanomaterials; LI-FRAUMENI-SYNDROME; DNA-BINDING DOMAIN; CANCER-ASSOCIATED MUTANT; TP53 MUTATION DATABASE; S-ALKYL THIOESTER; C-TERMINAL DOMAIN; WILD-TYPE P53; OLIGOMERIZATION DOMAIN; CRYSTAL-STRUCTURE; NUCLEAR EXPORT;
D O I
10.1002/bip.22772
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tetramer formation of p53 is essential for its tumor suppressor function. p53 not only acts as a tumor suppressor protein by inducing cell cycle arrest and apoptosis in response to genotoxic stress, but it also regulates other cellular processes, including autophagy, stem cell self-renewal, and reprogramming of differentiated cells into stem cells, immune system, and metastasis. More than 50% of human tumors have TP53 gene mutations, and most of them are missense mutations that presumably reduce tumor suppressor activity of p53. This review focuses on the role of the tetramerization (oligomerization), which is modulated by the protein concentration of p53, posttranslational modifications, and/or interactions with its binding proteins, in regulating the tumor suppressor function of p53. Functional control of p53 by stabilizing or inhibiting oligomer formation and its bio-applications are also discussed. (C) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:598 / 612
页数:15
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