Olivia Newton-John Cancer Research Institute and School of Cancer Medicine, La Trobe University, Heidelberg, VIC, 3084, Australia.
Walter and Eliza Hall Institute of Medical Research (WEHI), Parkville, VIC, 3010, Australia.
Cell Death Dis. 2024 Apr 10;15(4):255. doi: 10.1038/s41419-024-06631-8.
Excessive STAT3 signalling via gp130, the shared receptor subunit for IL-6 and IL-11, contributes to disease progression and poor survival outcomes in patients with colorectal cancer. Here, we provide evidence that bazedoxifene inhibits tumour growth via direct interaction with the gp130 receptor to suppress IL-6 and IL-11-mediated STAT3 signalling. Additionally, bazedoxifene combined with chemotherapy synergistically reduced cell proliferation and induced apoptosis in patient-derived colon cancer organoids. We elucidated that the primary mechanism of anti-tumour activity conferred by bazedoxifene treatment occurs via pro-apoptotic responses in tumour cells. Co-treatment with bazedoxifene and the SMAC-mimetics, LCL161 or Birinapant, that target the IAP family of proteins, demonstrated increased apoptosis and reduced proliferation in colorectal cancer cells. Our findings provide evidence that bazedoxifene treatment could be combined with SMAC-mimetics and chemotherapy to enhance tumour cell apoptosis in colorectal cancer, where gp130 receptor signalling promotes tumour growth and progression.
通过 gp130(IL-6 和 IL-11 的共同受体亚基)过度激活 STAT3 信号通路会促进结直肠癌患者的疾病进展和预后不良。本研究提供了证据表明,巴泽多昔芬通过与 gp130 受体直接相互作用抑制 IL-6 和 IL-11 介导的 STAT3 信号通路,从而抑制肿瘤生长。此外,巴泽多昔芬联合化疗可协同减少患者来源的结肠癌类器官中的细胞增殖并诱导细胞凋亡。我们阐明了巴泽多昔芬治疗赋予的抗肿瘤活性的主要机制是通过肿瘤细胞中的促凋亡反应。与 SMAC 模拟物 LCL161 或 Birinapant(靶向 IAP 蛋白家族)联合治疗时,可观察到结直肠癌细胞中的凋亡增加和增殖减少。我们的研究结果提供了证据表明,巴泽多昔芬治疗可与 SMAC 模拟物和化疗联合使用,以增强结直肠癌中 gp130 受体信号促进肿瘤生长和进展的肿瘤细胞凋亡。