Gan Xia, Liu Yonghong, Wang Xueni
Guangxi Zhuang Yao Medicine Center of Engineering and Technology, Guangxi University of Chinese Medicine, 13 Wuhe Road, Qingxiu District, Nanning 530200, China; Guangxi key laboratory of marine drugs, Institute of marine drugs, Guangxi University of Chinese Medicine, 13 Wuhe Road, Qingxiu District, Nanning 530200, China.
Guangxi key laboratory of marine drugs, Institute of marine drugs, Guangxi University of Chinese Medicine, 13 Wuhe Road, Qingxiu District, Nanning 530200, China.
Crit Rev Oncol Hematol. 2023 Nov;191:104142. doi: 10.1016/j.critrevonc.2023.104142. Epub 2023 Sep 24.
Glioblastomas are primary brain tumors that originate from glial stem cells or progenitor cells. There is a large difference in the incidence of glioblastoma between males and females. Studies revealed that the gender differences in the tumor may be attributable to the androgen receptor signaling axis. The incidence rate of glioblastoma in men is higher than that in women. Aberrant activation of the androgen receptor signaling pathway, or interactions between the androgen receptor signaling axis and other signaling axes promote the development of glioblastoma. Therefore, targeting the androgen receptor holds promise as a therapeutic approach for glioblastoma. This review investigates the dynamics of drug research into the treatment of glioblastoma by targeting the androgen receptor. The first finding in line with expectations is that androgen receptor antagonists, represented by enzalutamide, have been studied and shown to have anti-glioblastoma effects. In addition, it was found that the combination of 5-alpha reductase inhibitors and androgen receptor antagonists resulted in better therapeutic outcomes than each of them alone. Similar results were obtained with the combination of an epidermal growth factor receptor inhibitor and an androgen receptor antagonist. In addition, four small molecule compounds have been shown to exert significant anti-glioblastoma effects by directly or indirectly targeting the androgen receptor. Expectantly, one of these small molecules, seviteronel, progressed to the phase II clinical trial stage. These findings suggest that targeting the androgen receptor for glioblastoma may be a promising therapeutic option.
胶质母细胞瘤是起源于神经胶质干细胞或祖细胞的原发性脑肿瘤。男性和女性胶质母细胞瘤的发病率存在很大差异。研究表明,肿瘤中的性别差异可能归因于雄激素受体信号轴。男性胶质母细胞瘤的发病率高于女性。雄激素受体信号通路的异常激活,或雄激素受体信号轴与其他信号轴之间的相互作用促进了胶质母细胞瘤的发展。因此,靶向雄激素受体有望成为治疗胶质母细胞瘤的一种方法。本综述研究了靶向雄激素受体治疗胶质母细胞瘤的药物研究动态。第一个符合预期的发现是,以恩杂鲁胺为代表的雄激素受体拮抗剂已被研究并显示具有抗胶质母细胞瘤作用。此外,还发现5-α还原酶抑制剂和雄激素受体拮抗剂联合使用比单独使用每种药物产生更好的治疗效果。表皮生长因子受体抑制剂和雄激素受体拮抗剂联合使用也获得了类似的结果。此外,四种小分子化合物已被证明通过直接或间接靶向雄激素受体发挥显著的抗胶质母细胞瘤作用。预期这些小分子之一,司维特罗奈,已进入II期临床试验阶段。这些发现表明,靶向雄激素受体治疗胶质母细胞瘤可能是一种有前景的治疗选择。