有丝分裂MTH1抑制剂治疗癌症。

Q2 Medicine
Thomas Helleday
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引用次数: 0

摘要

DNA损伤反应(DDR)蛋白MTH1净化氧化dNTP池,防止氧化损伤进入DNA,并在有丝分裂中发挥新作用。它是一种应激诱导蛋白,经常被发现在癌症中过度表达。有丝分裂MTH1抑制剂在有丝分裂中阻止细胞,导致氧化损伤合并到DNA和选择性杀死癌细胞。在这里,我讨论了主要的有丝分裂MTH1抑制剂TH1579 (OXC-101, karonudib),目前正在临床试验中进行评估,并描述了它对癌细胞有丝分裂和氧化DNA损伤合并的双重作用。我描述了为什么仅仅抑制酶活性的MTH1抑制剂不能杀死癌细胞,并讨论了MTH1是否是癌症治疗的有效靶点。我讨论了MTH1在调节微管蛋白聚合和有丝分裂中的新作用,以及发展基础科学见解以及转化努力的必要性。我还给出了一个关于边缘扰动如何使DDR领域的目标验证变得困难的观点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mitotic MTH1 Inhibitors in Treatment of Cancer.

The DNA damage response (DDR) protein MTH1 is sanitising the oxidized dNTP pool and preventing incorporation of oxidative damage into DNA and has an emerging role in mitosis. It is a stress-induced protein and often found to be overexpressed in cancer. Mitotic MTH1 inhibitors arrest cells in mitosis and result in incorporation of oxidative damage into DNA and selective killing of cancer cells. Here, I discuss the leading mitotic MTH1 inhibitor TH1579 (OXC-101, karonudib), now being evaluated in clinical trials, and describe its dual effect on mitosis and incorporation of oxidative DNA damage in cancer cells. I describe why MTH1 inhibitors that solely inhibits the enzyme activity fail to kill cancer cells and discuss if MTH1 is a valid target for cancer treatment. I discuss emerging roles of MTH1 in regulating tubulin polymerisation and mitosis and the necessity of developing the basic science insights along with translational efforts. I also give a perspective on how edgetic perturbation is making target validation difficult in the DDR field.

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来源期刊
Cancer treatment and research
Cancer treatment and research Medicine-Oncology
CiteScore
1.00
自引率
0.00%
发文量
11
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