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在哺乳动物正呼肠孤病毒感染的早期阶段,前列腺癌细胞中 HIF-1α 的积累被抑制。

Inhibition of HIF-1α accumulation in prostate cancer cells is initiated during early stages of mammalian orthoreovirus infection.

机构信息

Department of Veterinary Microbiology and Preventive Medicine, College of Veterinary Medicine, Iowa State University, Ames, IA, 50011, USA.

Department of Veterinary Microbiology and Preventive Medicine, College of Veterinary Medicine, Iowa State University, Ames, IA, 50011, USA.

出版信息

Virology. 2021 Jun;558:38-48. doi: 10.1016/j.virol.2021.02.014. Epub 2021 Mar 7.

Abstract

Mammalian orthoreovirus (MRV) is a safe and effective cancer killing virus that has completed Phase I-III clinical trials against numerous cancer types. While many patients experience benefit from MRV therapy, pre-defined set points necessary for FDA approval have not been reached. Therefore, additional research into MRV biology and the effect of viral therapy on different tumor genetic subtypes and microenvironments is necessary to identify tumors most amenable to MRV virotherapy. In this work we analyzed the stage of viral infection necessary to inhibit HIF-1α, an aggressive cancer activator induced by hypoxia. We demonstrated that two viral capsid proteins were not necessary and that a step parallel with virus core movement across the endosomal membrane was required for this inhibition. Altogether, this work clarifies the mechanisms of MRV-induced HIF-1α inhibition and provides biological relevance for using MRV to inhibit the devastating effects of tumor hypoxia.

摘要

哺乳动物正呼肠孤病毒(MRV)是一种安全有效的杀癌病毒,已完成针对多种癌症类型的 I-III 期临床试验。虽然许多患者从 MRV 治疗中获益,但尚未达到 FDA 批准所需的预设标准。因此,需要对 MRV 生物学和病毒治疗对不同肿瘤遗传亚型和微环境的影响进行更多研究,以确定最适合 MRV 病毒治疗的肿瘤。在这项工作中,我们分析了抑制 HIF-1α所需的病毒感染阶段,HIF-1α是一种由缺氧诱导的侵袭性癌症激活因子。我们证明了两种病毒外壳蛋白不是必需的,并且在病毒核心穿过内体膜的运动过程中需要一个平行的步骤来抑制 HIF-1α。总的来说,这项工作阐明了 MRV 诱导的 HIF-1α抑制的机制,并为使用 MRV 抑制肿瘤缺氧的破坏性影响提供了生物学相关性。

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