Abstract 711: Repurposing 2ndgeneration androgen receptor antagonist Proxalutamide to treat COVID-19

Liandong Ma, Y. Tong, Q. Guo, Yifeng Zhou, Qianxiang Zhou, H. Yan
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Abstract

To date, as of 17 November 2020, there have been 55 million confirmed cases of COVID-19, including 1,4 million deaths globally, as reported to WHO. It is, therefore, very critical to discovery and development of the available treatment options for COVID-19. We here discuss the repurposing 2nd generation androgen receptor antagonist Proxalutaminde to treat COVID19. We analyzed the gender disparity of disease severity and progression in 1339 patients with COVID-19 and investigated the mechanism of gender disparity in male vs female patients with COVID 19. As androgen-androgen receptor pathway may contribute to the difference in severity and disease progression in male and female patients with COVID-19, we used cell lines derived from lung, prostate cancer and normal lung epithelial cells to determine the effect of androgen and androgen receptor antagonist Proxalutamide on the expression of two key proteins for SARS-CoV-2 to infect and enter the host cells. Angiotensin converting enzyme 2 (ACE2), a host transmembrane protein provides the binding sites for SARS-CoV-2 on the host cell surface, transmembrane protease serine 2 (TMPRSS2), a cellular serine protease, prims the S protein of SARS-Cov-2 to facilitate the viral entry into the host cells. As cytokine store plays a major role in the disease progression of COVID-19, we examined the effect of GT0918 on inducible nitric oxide synthase (iNOS) and Tumor necrosis factor-alpha (TNF-α), the macrophage polarization/activation markers, in mouse macrophage cells. In this study, we demonstrated higher rates of disease progression and mortality of male COVID-19 patients than female patients. Furthermore, we revealed that androgen-AR activation induced the expression of ACE2 and TMPRSS2 under the androgen-dependent condition in cells derived from prostate and lung cancer, which was inhibited by the blockage of AR signaling with Proxalutamide. Importantly, Proxalutamide also inhibited the expression of iNOS and TNF-α, the biomarkers for macrophage polarization/activation. These results support the role of androgen-AR signaling in the disease progression and mortality in male patients with COVID-19. We are currently conducting clinical study in COVID-19 patients with Proxalutamide in Brazil (NCT04446429). Citation Format: Liandong Ma, Youzhi Tong, Qiang Guo, Yifeng Zhou, Qianxiang Zhou, Honghua Yan. Repurposing 2nd generation androgen receptor antagonist Proxalutamide to treat COVID-19 [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2021; 2021 Apr 10-15 and May 17-21. Philadelphia (PA): AACR; Cancer Res 2021;81(13_Suppl):Abstract nr 711.
摘要:第二代雄激素受体拮抗剂Proxalutamide治疗COVID-19
据向世卫组织报告,截至2020年11月17日,全球已有5500万例COVID-19确诊病例,包括140万例死亡。因此,这对于发现和开发COVID-19的现有治疗方案至关重要。我们在这里讨论重新利用第二代雄激素受体拮抗剂proxalutamine治疗covid - 19。我们分析了1339例COVID-19患者疾病严重程度和进展的性别差异,探讨了男女COVID-19患者性别差异的机制。由于雄激素-雄激素受体通路可能与男性和女性COVID-19患者严重程度和疾病进展的差异有关,我们利用来自肺癌、前列腺癌和正常肺上皮细胞的细胞系,研究雄激素和雄激素受体拮抗剂Proxalutamide对SARS-CoV-2感染和进入宿主细胞的两种关键蛋白表达的影响。血管紧张素转换酶2 (ACE2)是一种宿主跨膜蛋白,为SARS-CoV-2在宿主细胞表面提供结合位点;细胞丝氨酸蛋白酶TMPRSS2 (TMPRSS2)引物SARS-CoV-2的S蛋白,促进病毒进入宿主细胞。由于细胞因子储存在COVID-19疾病进展中起重要作用,我们研究了GT0918对小鼠巨噬细胞诱导型一氧化氮合酶(iNOS)和肿瘤坏死因子-α (TNF-α)的影响,这些标志物是巨噬细胞极化/激活的标志物。在这项研究中,我们证实了男性COVID-19患者的疾病进展率和死亡率高于女性患者。此外,我们发现雄激素-AR激活可诱导前列腺癌和肺癌细胞在雄激素依赖条件下ACE2和TMPRSS2的表达,而Proxalutamide阻断AR信号通路可抑制ACE2和TMPRSS2的表达。重要的是,Proxalutamide还抑制巨噬细胞极化/激活的生物标志物iNOS和TNF-α的表达。这些结果支持雄激素- ar信号在男性COVID-19患者疾病进展和死亡率中的作用。我们目前正在巴西对使用Proxalutamide (NCT04446429)的COVID-19患者进行临床研究。引用格式:马连东,童友志,郭强,周一峰,周倩祥,闫宏华。第二代雄激素受体拮抗剂Proxalutamide治疗COVID-19[摘要]。见:美国癌症研究协会2021年年会论文集;2021年4月10日至15日和5月17日至21日。费城(PA): AACR;癌症杂志,2021;81(13 -增刊):摘要第711期。
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