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NSC95397是一种新型的HIV-1潜伏逆转剂。

NSC95397 is a Novel HIV-1 Latency Reversing Agent.

作者信息

Doyle Randilea Nichols, Yang Vivian, Kayode Yetunde I, Damoiseaux Robert, Taylor Harry E, Fregoso Oliver I

机构信息

Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, California, USA.

Molecular Biology Institute, University of California, Los Angeles, California, USA.

出版信息

bioRxiv. 2024 Aug 26:2023.05.24.542213. doi: 10.1101/2023.05.24.542213.

Abstract

The latent viral reservoir represents one of the major barriers of curing HIV-1. Focus on the "kick and kill" approach, in which virus expression is reactivated then cells producing virus are selectively depleted, has led to the discovery of many latency reversing agents (LRAs) that have furthered our understanding of the mechanisms driving HIV-1 latency and latency reversal. Thus far, individual compounds have yet to be robust enough to work as a therapy, highlighting the importance of identifying new compounds that target novel pathways and synergize with known LRAs. In this study, we identified a promising LRA, NSC95397, from a screen of ~4250 compounds. We validated that NSC95397 reactivates latent viral transcription and protein expression from cells with unique integration events and across different latency models. Co-treating cells with NSC95397 and known LRAs demonstrated that NSC95397 synergizes with different drugs under both standard normoxic and physiological hypoxic conditions. NSC95397 does not globally increase open chromatin, and bulk RNA sequencing revealed NSC95397 does not greatly increase cellular transcription. Instead, NSC95397 downregulates pathways key to metabolism, cell growth, and DNA repair - highlighting the potential of these pathways in regulating HIV-1 latency. Overall, we identified NSC95397 as a novel LRA that does not largely alter global transcription, that shows potential for synergy with known LRAs, and that may act through novel pathways not previously recognized for their ability to modulate HIV-1 latency.

摘要

潜伏性病毒储存库是治愈HIV-1的主要障碍之一。聚焦于“激活并清除”策略,即重新激活病毒表达然后选择性清除产生病毒的细胞,已促使人们发现了许多潜伏逆转剂(LRA),这些试剂加深了我们对驱动HIV-1潜伏和潜伏逆转机制的理解。到目前为止,单个化合物还不够强大,无法作为一种疗法发挥作用,这凸显了识别靶向新途径并与已知LRA协同作用的新化合物的重要性。在本研究中,我们从约4250种化合物的筛选中鉴定出一种有前景的LRA,NSC95397。我们验证了NSC95397能重新激活具有独特整合事件的细胞以及不同潜伏模型中的潜伏病毒转录和蛋白质表达。用NSC95397和已知LRA共同处理细胞表明,在标准常氧和生理性低氧条件下,NSC95397都能与不同药物协同作用。NSC95397不会全局性地增加开放染色质,大量RNA测序显示NSC95397不会大幅增加细胞转录。相反,NSC95397下调了代谢、细胞生长和DNA修复的关键途径——这凸显了这些途径在调节HIV-1潜伏方面的潜力。总体而言,我们将NSC95397鉴定为一种新型LRA,它不会在很大程度上改变全局转录,显示出与已知LRA协同作用的潜力,并且可能通过以前未因其调节HIV-1潜伏的能力而被认识的新途径发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f357/11423059/159d62304f52/nihpp-2023.05.24.542213v2-f0001.jpg

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