Department of Pediatric Surgery, Tongji Hospital.
The Research Institute at Nationwide Children's Hospital, The Ohio State University.
J Pediatr Hematol Oncol. 2024 Jan 1;46(1):8-14. doi: 10.1097/MPH.0000000000002782. Epub 2023 Nov 13.
Osteosarcoma is the most common primary bone tumor. Using the multiple ligands simultaneous docking method, we found that bazedoxifene could bind to the GP130 D1 domain. We then demonstrated that bazedoxifene can decrease cell viability and cell migration of osteosarcoma cells by inhibiting interleukin 6 (IL-6) and IL-11/GP130 signaling. Consistently, treatment with IL-6 or IL-11 antibody or knockdown of GP130 by siRNA silenced the activation of STAT3, ERK, and AKT. Similarly, recombinant IL-6 and IL-11 proteins antagonized the inhibitory effect of bazedoxifene on osteosarcoma cells. Finally, the combinational treatment of temsirolimus and bazedoxifene synergistically suppressed osteosarcoma development in vitro and in vivo. Our findings suggest that bazedoxifene directly prompts the deactivation of GP130 and inhibits the osteosarcoma progression in vitro and in vivo. Therefore, bazedoxifene could be effectively applied as a therapeutic drug for human osteosarcoma in the future.
骨肉瘤是最常见的原发性骨肿瘤。我们采用多个配体同时对接的方法发现,巴泽多昔芬可以与 GP130 D1 结构域结合。我们进一步证明,巴泽多昔芬可以通过抑制白细胞介素 6(IL-6)和 IL-11/GP130 信号通路来降低骨肉瘤细胞的活力和迁移。一致地,使用 IL-6 或 IL-11 抗体处理或通过 siRNA 敲低 GP130 可以沉默 STAT3、ERK 和 AKT 的激活。同样,重组 IL-6 和 IL-11 蛋白拮抗了巴泽多昔芬对骨肉瘤细胞的抑制作用。最后,替西罗莫司和巴泽多昔芬的联合治疗在体外和体内协同抑制骨肉瘤的发展。我们的研究结果表明,巴泽多昔芬直接促使 GP130 失活,并抑制骨肉瘤在体外和体内的进展。因此,巴泽多昔芬将来可能会被有效地应用于人类骨肉瘤的治疗药物。