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合成致死性在抗癌治疗药物研发中的应用与研究进展

Application and research progress of synthetic lethality in the development of anticancer therapeutic drugs.

作者信息

Gong Xiaoliang, Liu Chunxi, Tang Haoyang, Wu Song, Yang Qingyun

机构信息

State Key Laboratory of Bioactive Substance and Function of Natural Medicines, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.

出版信息

Front Oncol. 2024 Nov 25;14:1460412. doi: 10.3389/fonc.2024.1460412. eCollection 2024.

Abstract

With the tremendous success of the PARP inhibitor olaparib in clinical practice, synthetic lethality has become an important field for the discovery and development of anticancer drugs. More and more synthetic lethality targets have been discovered with the rapid development of biotechnology in recent years. Currently, many drug candidates that were designed and developed on the basis of the concept of synthetic lethality have entered clinical trials. Taking representative synthetic lethal targets Poly ADP-ribose polymerase 1 (PARP1), Werner syndrome helicase (WRN) and protein arginine methyltransferase 5 (PRMT5) as examples, this article briefly discusses the application and research progress of synthetic lethality in the development of anticancer drugs.

摘要

随着聚(ADP - 核糖)聚合酶抑制剂奥拉帕尼在临床实践中取得巨大成功,合成致死性已成为抗癌药物发现与开发的一个重要领域。近年来,随着生物技术的快速发展,越来越多的合成致死性靶点被发现。目前,许多基于合成致死性概念设计和开发的候选药物已进入临床试验阶段。本文以具有代表性的合成致死性靶点聚(ADP - 核糖)聚合酶1(PARP1)、沃纳综合征解旋酶(WRN)和蛋白质精氨酸甲基转移酶5(PRMT5)为例,简要探讨合成致死性在抗癌药物开发中的应用及研究进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eef6/11625670/c304502778a5/fonc-14-1460412-g001.jpg

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