PRMT阻塞诱导了缺陷的DNA复制应激反应,并与PARP抑制产生协同作用
Yang Li1, Lacey E Dobrolecki2, Christina Sallas2
1Department of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Cell reports. Medicine
|December 20, 2023
概括
用抑制剂向蛋白质阿尔金因甲基转移酶 (PRMTs) 抑制ATR,这是一个关键的DNA修复蛋白. 将PRMT5抑制与PARP抑制剂的结合显示为癌症治疗的前景.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 在多种癌症中观察到PRMT1,PRMT4和PRMT5的异常蛋白质氨酸甲基化.
- 在细胞过程中,PRMTs起着至关重要的作用,包括DNA修复和应激反应.
研究的目的:
- 研究抑制PRMT1,PRMT4和PRMT5对癌细胞系的影响.
- 为了确定将PRMT抑制与PARP抑制剂相结合的治疗潜力.
主要方法:
- 针对性蛋白质组学用于分析12个癌症细胞系中PRMT抑制后的蛋白质水平.
- 该研究评估了PRMT抑制对ATR水平和DNA复制应激反应的影响.
- PRMT和PARP抑制剂的协同效应在体外和体内被评估.
主要成果:
- 抑制I型和II型PRMTs导致酸化和总ATR的抑制.
- 抑制PRMT导致缺陷的DNA复制应激反应激活,增强PARP抑制剂的有效性.
- PRMT5和PARP抑制剂的联合治疗证明了患者衍生异体移植的改善生存率,没有观察到毒性.
结论:
- 抑制PRMT,特别是PRMT5,可以使瘤对PARP抑制剂敏感.
- PRMT5和PARP抑制的组合代表了对各种癌症的潜在耐受性良好和有效的治疗策略,无论同源重组状态如何.
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