Institute for Developmental Immunology, Biocenter, Medical University of Innsbruck, Austria.
Institute for Medical Biochemistry, Biocenter, Medical University of Innsbruck, Austria.
Mol Oncol. 2022 Aug;16(15):2771-2787. doi: 10.1002/1878-0261.13264. Epub 2022 Jul 7.
Checkpoint kinase 1 (CHK1; encoded by CHEK1) is an essential gene that monitors DNA replication fidelity and prevents mitotic entry in the presence of under-replicated DNA or exogenous DNA damage. Cancer cells deficient in p53 tumor suppressor function reportedly develop a strong dependency on CHK1 for proper cell cycle progression and maintenance of genome integrity, sparking interest in developing kinase inhibitors. Pharmacological inhibition of CHK1 triggers B-Cell CLL/Lymphoma 2 (BCL2)-regulated cell death in malignant cells largely independently of p53, and has been suggested to kill p53-deficient cancer cells even more effectively. Next to p53 status, our knowledge about factors predicting cancer cell responsiveness to CHK1 inhibitors is limited. Here, we conducted a genome-wide CRISPR/Cas9-based loss-of-function screen to identify genes defining sensitivity to chemical CHK1 inhibitors. Next to the proapoptotic BCL2 family member, BCL2 Binding Component 3 (BBC3; also known as PUMA), the F-box protein S-phase Kinase-Associated Protein 2 (SKP2) was validated to tune the cellular response to CHK1 inhibition. SKP2 is best known for degradation of the Cyclin-dependent Kinase Inhibitor 1B (CDKN1B; also known as p27), thereby promoting G1-S transition and cell cycle progression in response to mitogens. Loss of SKP2 resulted in the predicted increase in p27 protein levels, coinciding with reduced DNA damage upon CHK1-inhibitor treatment and reduced cell death in S-phase. Conversely, overexpression of SKP2, which consequently results in reduced p27 protein levels, enhanced cell death susceptibility to CHK1 inhibition. We propose that assessing SKP2 and p27 expression levels in human malignancies will help to predict the responsiveness to CHK1-inhibitor treatment.
细胞周期检查点激酶 1(CHK1;由 CHEK1 编码)是一种必需基因,可监测 DNA 复制保真度,并在存在未复制 DNA 或外源性 DNA 损伤的情况下阻止有丝分裂进入。据报道,缺乏抑癌基因 p53 功能的癌细胞对 CHK1 有很强的依赖性,以正确进行细胞周期进程并维持基因组完整性,这激发了开发激酶抑制剂的兴趣。CHK1 的药理学抑制在很大程度上独立于 p53 触发 B 细胞慢性淋巴细胞白血病/淋巴瘤 2(BCL2)调节的细胞死亡,并被认为可以更有效地杀死 p53 缺失的癌细胞。除了 p53 状态外,我们对预测癌细胞对 CHK1 抑制剂反应的因素的了解有限。在这里,我们进行了基于全基因组 CRISPR/Cas9 的功能丧失筛选,以鉴定定义对化学 CHK1 抑制剂敏感性的基因。除了促凋亡的 BCL2 家族成员 BCL2 结合成分 3(BBC3;也称为 PUMA)外,F-box 蛋白 S 期激酶相关蛋白 2(SKP2)也被验证可调节细胞对 CHK1 抑制的反应。SKP2 最著名的是降解细胞周期蛋白依赖性激酶抑制剂 1B(CDKN1B;也称为 p27),从而促进细胞周期从 G1 期向 S 期过渡和细胞周期进程,以响应有丝分裂原。SKP2 的缺失导致预测的 p27 蛋白水平增加,同时在 CHK1 抑制剂治疗时减少 DNA 损伤,并在 S 期减少细胞死亡。相反,SKP2 的过表达会导致 p27 蛋白水平降低,从而增强对 CHK1 抑制剂的细胞死亡敏感性。我们提出,评估人类恶性肿瘤中的 SKP2 和 p27 表达水平将有助于预测对 CHK1 抑制剂治疗的反应性。