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肿瘤抑制因子p53及其癌症相关突变体的结构生物学

Structural biology of the tumor suppressor p53 and cancer-associated mutants.

作者信息

Joerger Andreas C, Fersht Alan R

机构信息

MRC Centre for Protein Engineering, Cambridge CB2 2QH, United Kingdom.

出版信息

Adv Cancer Res. 2007;97:1-23. doi: 10.1016/S0065-230X(06)97001-8.

Abstract

The tumor suppressor protein p53 is a transcription factor that plays a key role in the prevention of cancer development. In response to oncogenic or other stresses, the p53 protein is activated and regulates the expression of a variety of target genes, resulting in cell cycle arrest, senescence, or apoptosis. Mutation of the p53 gene is the most common genetic alteration in human cancer, affecting more than 50% of human tumors. Most of these mutations inactivate the DNA-binding domain of the protein. In this chapter, we describe the structure of the wild-type p53 protein and present structural and functional data that provide the molecular basis for understanding the effects of common cancer mutations. Further, we assess novel therapeutic strategies that aim to rescue the function of p53 cancer mutants.

摘要

肿瘤抑制蛋白p53是一种转录因子,在预防癌症发展中起关键作用。响应致癌或其他应激,p53蛋白被激活并调节多种靶基因的表达,导致细胞周期停滞、衰老或凋亡。p53基因的突变是人类癌症中最常见的基因改变,影响超过50%的人类肿瘤。这些突变大多使该蛋白的DNA结合结构域失活。在本章中,我们描述野生型p53蛋白的结构,并呈现结构和功能数据,这些数据为理解常见癌症突变的影响提供了分子基础。此外,我们评估旨在挽救p53癌症突变体功能的新型治疗策略。

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