Evidence map›Paper›PMID 37293110›Full record

ArticlebioRxiv : the preprint server for biology2024

NSC95397 is a Novel HIV-1 Latency Reversing Agent.

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

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Randilea Nichols DoyleDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, California, USA.
Vivian YangDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, California, USA.
Yetunde I KayodeDepartment of Microbiology and Immunology, State University of New York (SUNY) Upstate Medical University, Syracuse, NY.
Robert DamoiseauxCalifornia NanoSystems Institute, University of California, Los Angeles, California, USA.
Harry E TaylorDepartment of Microbiology and Immunology, State University of New York (SUNY) Upstate Medical University, Syracuse, NY.
Oliver I FregosoDepartment of Microbiology, Immunology, and Molecular Genetics, University of California, Los Angeles, California, USA.ORCID 0000-0003-3087-3374
University of California, Los Angeles · USSUNY Upstate Medical University · USCalifornia NanoSystems Institute · US

Funding

UCLA-CDU CFARP30AI152501 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SCOTT G KITCHEN · 2022 to 2026
$15.6M
NIAID NIH HHS P30 AI152501
6 · The paper itself

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.

Identifiers

PMID37293110
PMCPMC10245985
OpenAlexW4378211575

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.