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