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BET 抑制剂 I-BET762 与 PARP 抑制剂他拉唑帕尼在小细胞肺癌细胞中的协同作用。

BET-Inhibitor I-BET762 and PARP-Inhibitor Talazoparib Synergy in Small Cell Lung Cancer Cells.

机构信息

Department of Biomedical Science, and National Institute of Biostructures and Biosystems, University of Sassari, 07100 Sassari, Italy.

Kitos Biotech Srls, Porto Conte Ricerche, 07041 Alghero, Italy.

出版信息

Int J Mol Sci. 2020 Dec 16;21(24):9595. doi: 10.3390/ijms21249595.

Abstract

Small cell lung cancer (SCLC) is an aggressive type of lung cancer with high mortality that is caused by frequent relapses and acquired resistance. Despite that several target-based approaches with potential therapeutic impact on SCLC have been identified, numerous targeted drugs have not been successful in providing improvements in cancer patients when used as single agents. A combination of targeted therapies could be a strategy to induce maximum lethal effects on cancer cells. As a starting point in the development of new drug combination strategies for the treatment of SCLC, we performed a mid-throughput screening assay by treating a panel of SCLC cell lines with BETi or AKi in combination with PARPi or EZH2i. We observed drug synergy between I-BET762 and Talazoparib, BETi and PARPi, respectively, in SCLC cells. Combinatorial efficacy was observed in -amplified and -wt SCLC cells over SCLC cells with impaired MYC signaling pathway or non-tumor cells. We indicate that drug synergy between I-BET762 and Talazoparib is associated with the attenuation HR-DSBR process and the downregulation of various players of DNA damage response by BET inhibition, such as CHEK2, PTEN, NBN, and FANCC. Our results provide a rationale for the development of new combinatorial strategies for the treatment of SCLC.

摘要

小细胞肺癌(SCLC)是一种侵袭性肺癌,死亡率高,其频繁复发和获得性耐药是导致这一现象的主要原因。尽管已经确定了几种基于靶点的方法对 SCLC 具有潜在的治疗作用,但许多靶向药物作为单一药物在癌症患者中并未成功改善病情。联合使用靶向治疗可能是一种策略,可以对癌细胞产生最大的致死作用。作为开发用于治疗 SCLC 的新药联合策略的起点,我们通过用 BETi 或 AKi 联合 PARPi 或 EZH2i 处理一组 SCLC 细胞系进行了中通量筛选试验。我们观察到 BETi 和 PARPi 分别在 SCLC 细胞中 I-BET762 和 Talazoparib 之间存在药物协同作用。在 SCLC 细胞中,观察到在 MYC 信号通路受损或非肿瘤细胞中,-扩增和 -wt SCLC 细胞的组合疗效。我们表明,I-BET762 和 Talazoparib 之间的药物协同作用与 HR-DSBR 过程的衰减以及 BET 抑制下调各种 DNA 损伤反应的参与者有关,例如 CHEK2、PTEN、NBN 和 FANCC。我们的结果为开发治疗 SCLC 的新联合策略提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc6/7766292/5136467cf467/ijms-21-09595-g001.jpg

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