Drug discovery targeting Chk1 and Chk2 kinases.

Progress in cell cycle research Pub Date : 2003-01-01
Bin-Bing S Zhou, Edward A Sausville
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Abstract

The DNA damage response includes not only checkpoint and apoptosis, but also direct activation of DNA repair networks. Downstream in the DNA damage response pathway are Chk1, an essential checkpoint kinase, and Chk2, which plays a critical role in p53-dependent apoptosis. Chk1 inhibition is expected to lead to chemosensitization of tumors, while Chk2 inhibition could protect normal sensitive tissues from some chemotherapeutic agents. Drugs targeting Chk1 and Chk2 have the potential to significantly improve the therapeutic window of DNA damaging agents available in the clinic.

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靶向Chk1和Chk2激酶的药物发现。
DNA损伤反应不仅包括检查点和细胞凋亡,还包括DNA修复网络的直接激活。DNA损伤反应通路的下游是Chk1,一种必需的检查点激酶,Chk2在p53依赖性细胞凋亡中起关键作用。Chk1抑制有望导致肿瘤的化学致敏,而Chk2抑制可以保护正常的敏感组织免受某些化疗药物的影响。靶向Chk1和Chk2的药物有可能显著改善临床可用的DNA损伤药物的治疗窗口。
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