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以p73为靶点的抗肿瘤药物研究进展

牟汉川 杨志宽 暴亚锋 张继虹

中国药理学通报2017,Vol.33Issue(9):1207-1210,4.
中国药理学通报2017,Vol.33Issue(9):1207-1210,4.DOI:10.3969/j.issn.1001-1978.2017.09.006

以p73为靶点的抗肿瘤药物研究进展

Advances in p73-targeting anti-tumor drugs

牟汉川 1杨志宽 1暴亚锋 1张继虹1

作者信息

  • 1. 昆明理工大学医学院衰老与肿瘤分子遗传学实验室,云南 昆明 650500
  • 折叠

摘要

Abstract

The transcription factor p73 belongs to the p53 family of tumor suppressors,and can be transcribed into different isoforms with either pro-or anti-apoptotic(TAp73 and △Np73)functions.However,the tumor suppressor activity of TAp73 is inhibited through complex formation with inhibitory proteins(e.g.△Np73,mutant p53,MDM2 and iASPP).Therefore,it is a kind of tumor therapy strategy to reactivate TAp73 through targeting these inhibitors directly or release TAp73 from the complex by targeting their interaction.This review discusses the possible strategies of targeting p73 for its reactivation and the acting mechanism of related compounds.

关键词

肿瘤抑制因子/p73/TAp73/凋亡/负调节因子/复合体

Key words

tumor suppressor/p73/TAp73/apoptosis/inhibitory proteins/complex

分类

医药卫生

引用本文复制引用

牟汉川,杨志宽,暴亚锋,张继虹..以p73为靶点的抗肿瘤药物研究进展[J].中国药理学通报,2017,33(9):1207-1210,4.

基金项目

国家自然科学基金资助项目(No 81560601) (No 81560601)

昆明理工大学分析测试基金项目(No 2016M2014236022) (No 2016M2014236022)

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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