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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.

机构信息

Department of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, CA 90095, USA.

Molecular Biology Institute, University of California, Los Angeles, CA 90095, USA.

出版信息

Viruses. 2024 Nov 16;16(11):1783. doi: 10.3390/v16111783.

Abstract

The latent viral reservoir represents one of the major barriers to curing HIV-1. Focus on the "kick and kill" (also called "shock and kill") approach, in which virus expression is reactivated, and 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 that 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, shows potential for synergy with known LRAs, and may act through novel pathways not previously recognized for their ability to modulate HIV-1 latency.

摘要

潜伏的病毒库是治愈 HIV-1 的主要障碍之一。关注“踢和杀”(也称为“冲击和杀伤”)方法,其中病毒表达被重新激活,然后选择性地耗尽产生病毒的细胞,这导致发现了许多潜伏逆转剂(LRAs),进一步加深了我们对驱动 HIV-1 潜伏和潜伏逆转的机制的理解。到目前为止,单个化合物还没有强大到足以作为一种治疗方法,这凸显了确定靶向新途径并与已知 LRA 协同作用的新化合物的重要性。在这项研究中,我们从大约 4250 种化合物的筛选中发现了一种有前途的 LRA,NSC95397。我们验证了 NSC95397 可重新激活具有独特整合事件和不同潜伏模型的细胞中的潜伏病毒转录和蛋白表达。在标准常氧和生理低氧条件下,将 NSC95397 与已知的 LRA 共同治疗细胞,证明 NSC95397 与不同药物具有协同作用。NSC95397 不会全局增加开放染色质,并且批量 RNA 测序表明 NSC95397 不会大大增加细胞转录。相反,NSC95397 下调代谢、细胞生长和 DNA 修复途径的关键途径-突出了这些途径在调节 HIV-1 潜伏中的潜在作用。总体而言,我们确定 NSC95397 是一种新型的 LRA,它不会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被认为能够调节 HIV-1 潜伏的新途径发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd36/11599149/1a4a67072615/viruses-16-01783-g001.jpg

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