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甲基化合成致死性:利用选择性药物靶点进行癌症治疗。

Methylation synthetic lethality: Exploiting selective drug targets for cancer therapy.

机构信息

Clinical Medicine, The Fourth Affiliated Hospital of China Medical University, Shenyang 110032, China.

Central Laboratory, The Fourth Affiliated Hospital of China Medical University, Shenyang 110032, China.

出版信息

Cancer Lett. 2024 Aug 10;597:217010. doi: 10.1016/j.canlet.2024.217010. Epub 2024 Jun 6.

Abstract

In cancer, synthetic lethality refers to the drug-induced inactivation of one gene and the inhibition of another in cancer cells by a drug, resulting in the death of only cancer cells; however, this effect is not present in normal cells, leading to targeted killing of cancer cells. Recent intensive epigenetic research has revealed that aberrant epigenetic changes are more frequently observed than gene mutations in certain cancers. Recently, numerous studies have reported various methylation synthetic lethal combinations involving DNA damage repair genes, metabolic pathway genes, and paralogs with significant results in cellular models, some of which have already entered clinical trials with promising results. This review systematically introduces the advantages of methylation synthetic lethality and describes the lethal mechanisms of methylation synthetic lethal combinations that have recently demonstrated success in cellular models. Furthermore, we discuss the future opportunities and challenges of methylation synthetic lethality in targeted anticancer therapies.

摘要

在癌症中,合成致死性是指药物诱导的一种基因失活和另一种基因在癌细胞中的抑制,导致只有癌细胞死亡;然而,这种效应在正常细胞中并不存在,从而导致对癌细胞的靶向杀伤。最近密集的表观遗传学研究表明,在某些癌症中,异常的表观遗传变化比基因突变更为常见。最近,许多研究报告了涉及 DNA 损伤修复基因、代谢途径基因和具有显著细胞模型结果的同源基因的各种甲基化合成致死组合,其中一些已经进入临床试验并取得了有希望的结果。本综述系统地介绍了甲基化合成致死性的优势,并描述了最近在细胞模型中成功证明的甲基化合成致死组合的致死机制。此外,我们还讨论了在靶向抗癌治疗中甲基化合成致死性的未来机遇和挑战。

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