Department of Cancer Biology. Cleveland Clinic Lerner Research Institute, Cleveland, Ohio.
Department of Translational Hematology and Oncology Research, Cleveland Clinic, Cleveland, Ohio.
Cancer Res. 2018 May 1;78(9):2396-2406. doi: 10.1158/0008-5472.CAN-17-1920. Epub 2018 Feb 13.
Traditional treatments of small-cell lung cancer (SCLC) with cisplatin, a standard-of-care therapy, spare the tumor-initiating cells (TIC) that mediate drug resistance. Here we report a novel therapeutic strategy that preferentially targets TICs in SCLC, in which cisplatin is combined with CBL0137, an inhibitor of the histone chaperone facilitates chromatin transcription (FACT), which is highly expressed in TICs. Combination of cisplatin and CBL0137 killed patient-derived and murine SCLC cell lines synergistically. In response to CBL0137 alone, TICs were more sensitive than non-TICs, in part, because CBL0137 increased expression of the tumor suppressor by abrogating the binding of negative regulator SP3 to the NOTCH1 promoter, and in part because treatment decreased the high expression of stem cell transcription factors. The combination of cisplatin and CBL0137 greatly reduced the growth of a patient-derived xenograft in mice and also the growth of a syngeneic mouse SCLC tumor. Thus, CBL0137 can be a highly effective drug against SCLC, especially in combination with cisplatin. These findings reveal a novel therapeutic regimen for SCLC, combining cisplatin with an inhibitor that preferentially targets tumor-initiating cells. .
传统的小细胞肺癌 (SCLC) 治疗方法是使用顺铂作为标准治疗药物,但这种方法会保留介导耐药性的肿瘤起始细胞 (TIC)。在这里,我们报告了一种新的治疗策略,该策略优先针对 SCLC 中的 TIC,其中顺铂与 CBL0137 联合使用,CBL0137 是组蛋白伴侣促进染色质转录 (FACT) 的抑制剂,在 TIC 中高度表达。顺铂和 CBL0137 的联合使用对患者来源和鼠源 SCLC 细胞系具有协同杀伤作用。单独使用 CBL0137 时,TIC 比非 TIC 更敏感,部分原因是 CBL0137 通过消除负调节因子 SP3 与 NOTCH1 启动子的结合,增加了肿瘤抑制因子 的表达,部分原因是治疗降低了干细胞转录因子的高表达。顺铂和 CBL0137 的联合使用大大减少了患者来源的异种移植小鼠肿瘤的生长,也减少了同基因小鼠 SCLC 肿瘤的生长。因此,CBL0137 可以成为一种非常有效的 SCLC 治疗药物,尤其是与顺铂联合使用时。这些发现揭示了一种针对 SCLC 的新治疗方案,将顺铂与一种优先针对肿瘤起始细胞的抑制剂联合使用。