药学学报, 2021, 56(4): 983-995
引用本文:
王继超, 杨采彬, 卓伊琳, 梁冲, 王俊钢, 董升, 李博腾, 张淑华, 张国刚*. MDM2-p53抑制剂的研究进展[J]. 药学学报, 2021, 56(4): 983-995.
WANG Ji-chao, YANG Cai-bin, ZHUO Yi-lin, LIANG Chong, WANG Jun-gang, DONG Sheng, LI Bo-teng, ZHANG Shu-hua, ZHANG Guo-gang*. Recent advances of MDM2-p53 inhibitors[J]. Acta Pharmaceutica Sinica, 2021, 56(4): 983-995.

MDM2-p53抑制剂的研究进展
王继超, 杨采彬, 卓伊琳, 梁冲, 王俊钢, 董升, 李博腾, 张淑华, 张国刚*
沈阳药科大学中药学院, 辽宁 沈阳 110016
摘要:
蛋白-蛋白相互作用(protein-protein interaction,PPI)参与包括细胞间的相互作用以及代谢和发育控制等多种生物学过程。PPI的错误调控、翻译后修饰和干扰与多种人类疾病有关,使得这些相互作用的调节成为药物发现的一个非常有吸引力的领域。其中,MDM2-p53蛋白与蛋白的相互作用是近年来的研究热点,在肿瘤的治疗中发挥着重要的作用,但遗憾的是国内外都没有该抑制剂上市。本文综述了近年来有关MDM2-p53抑制剂的研究进展并讨论了临床上有应用前景的MDM2-p53抑制剂。
关键词:    蛋白-蛋白相互作用      MDM2-p53      抑制剂      研究进展      临床应用     
Recent advances of MDM2-p53 inhibitors
WANG Ji-chao, YANG Cai-bin, ZHUO Yi-lin, LIANG Chong, WANG Jun-gang, DONG Sheng, LI Bo-teng, ZHANG Shu-hua, ZHANG Guo-gang*
School of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang 110016, China
Abstract:
Protein-protein interactions (PPI) are involved in a variety of biological processes, including cell-to-cell interactions, metabolism and development control. The misregulation, post-translational modification and interference of PPI are related to a variety of human diseases, making the regulation of these interactions a very attractive field of drug discovery. In recent years, the interaction between MDM2 and p53 has become a research hotspot, which plays an important role in the treatment of tumors. But unfortunately there are no such inhibitors approved all over the world. In this view, recent advances of MDM2-p53 inhibitors were briefly described and its inhibitors with potential therapeutic activities in clinical studies were introduced.
Key words:    protein-protein interaction    MDM2-p53    inhibitor    recent advance    clinical study   
收稿日期: 2020-09-04
DOI: 10.16438/j.0513-4870.2020-1454
基金项目: 沈阳药科大学大学生创新创业训练计划国家级项目(202010163023).
通讯作者: 张国刚,Tel:86-24-23986511,E-mail:zggth@163.com
Email: zggth@163.com
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