Abstract 713: Inhibition of pseudo SARS-CoV-2 binding activity of a anti-cancer polypharmacological agent analogs

R. Papineni, A. Adhikary, R. Tandon, Dipanwita Mitra
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引用次数: 2

Abstract

Severe acute respiratory syndrome coronavirus (SARS-CoV-2), a single-stranded RNA virus with largest genomes (∼ 29,800 bases) of all viruses, causes the infectious disease, COVID-19. SARS-CoV-2 is a zoonotic betacoronavirus transmitted through airborne and fecal-oral routes infecting nasal, lung, and intestinal tissues causing over 26 million confirmed coronavirus disease 2019 (COVID-19) cases and nearly 900,000 associated deaths worldwide as of September 2020. The surface of SARS-CoV-2 is covered with copies of spike glycoprotein (SGP) that plays a pivotal role in virus entry in host cells utilizing angiotensin-converting enzyme 2 (ACE2) as an attachment and entry receptor. We have successfully made a high titer replication-incompetent third-generation lentiviral vector pseudotyped with SARS-2-CoV SGP (pLV-S). Upon successful attachment and entry, the lentiviral vector causes enhanced green fluorescent protein (eGFP) to be expressed in the infected cell. Here, we show how the polypharmacological agent, 2-Deoxy-D-glucose (2-DG), a glucose mimic, and well characterized anti-cancer drug, and its analogs inhibit spike protein binding to the ACE2 receptors. This is as suggested from the 2DG and two analogs inhibition, with a low micromolar affinity, the pLV-S attachment and entry resulting in reduced cell fluorescence of infected HEK293 cells. In addition, we describe 2DG and analogs has the potential to deliver polypharmacological effects on the COVID-through inhibition of glycolysis (at energy status), modulation of inflammatory responses (cytokine storm) and alterations in glycosylation of viral proteins. A unique class of adjuvants and mitigants in the anti-SARS-CoV-2 activity is presented here. Citation Format: Rao V. Papineni, Amitava Adhikary, Ritesh Tandon, Dipanwita Mitra. Inhibition of pseudo SARS-CoV-2 binding activity of a anti-cancer polypharmacological agent analogs [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 713.
摘要:一种抗癌多药理学类似物对伪SARS-CoV-2结合活性的抑制作用
严重急性呼吸综合征冠状病毒(SARS-CoV-2)是一种单链RNA病毒,具有所有病毒中最大的基因组(约29,800个碱基),可引起COVID-19传染病。SARS-CoV-2是一种人畜共患的乙型冠状病毒,通过空气传播和粪口途径传播,感染鼻腔、肺部和肠道组织,截至2020年9月,在全球范围内造成2600多万例新冠状病毒(COVID-19)确诊病例和近90万例相关死亡。SARS-CoV-2表面覆盖着刺突糖蛋白(SGP)拷贝,该蛋白利用血管紧张素转换酶2 (ACE2)作为附着和进入受体,在病毒进入宿主细胞中起关键作用。我们成功地用SARS-2-CoV SGP (pLV-S)假型制备了高滴度复制能力不强的第三代慢病毒载体。在成功附着和进入后,慢病毒载体引起增强的绿色荧光蛋白(eGFP)在感染细胞中表达。在这里,我们展示了多药理学剂,2-脱氧- d -葡萄糖(2-DG),一种葡萄糖模拟物,以及表征良好的抗癌药物,及其类似物如何抑制刺突蛋白与ACE2受体的结合。这可以从2DG和两种类似物的低微摩尔亲和力抑制,pLV-S的附着和进入导致感染HEK293细胞的细胞荧光降低中得到证明。此外,我们描述了2DG和类似物有可能通过抑制糖酵解(能量状态)、调节炎症反应(细胞因子风暴)和改变病毒蛋白的糖基化,对covid - 19产生多药理学作用。本文介绍了一类具有抗sars - cov -2活性的独特佐剂和缓释剂。引文格式:Rao V. Papineni, Amitava Adhikary, Ritesh Tandon, Dipanwita Mitra。一种抗癌多药理学类似物抑制伪SARS-CoV-2结合活性的研究[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713期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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