Evidence map›Paper›PMID 30989696›Full record

ArticleJournal of medical virology2019

Curaxin CBL0137 has the potential to reverse HIV-1 latency.

Maxime J Jean, Dawei Zhou, Guillaume Fiches, Weili Kong, Huachao Huang, Andrei Purmal, Katerina Gurova, Netty G Santoso, Jian Zhu

Abstract read
In one paragraph

Article in Journal of medical virology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. A nucleosome switch primes Hepatitis B Virus infection.bioRxiv : the preprint server for biology · 2024
    Article
  6. Review
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Maxime J JeanDepartment of Microbiology and Immunology, University of Rochester Medical Center, Rochester, New York.
Dawei ZhouDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, Ohio.
Guillaume FichesDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, Ohio.
Weili KongDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, Ohio.
Huachao HuangDepartment of Medicine, Columbia University Medical Center, New York, New York.
Andrei PurmalDivision of Chemistry, Incuron LLC, Buffalo, New York.
Katerina GurovaDepartment of Cell Stress Biology, Roswell Park Cancer Institute, Buffalo, New York.
Netty G SantosoDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, Ohio.
Jian ZhuDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, Ohio.ORCID 0000-0001-9856-8320

Funding

University of Rochester Mentoring Environment: Nurturing Training Opportunities in Research (UR-MENTOR)T32GM007356 · NIGMS · UNIVERSITY OF ROCHESTER · PI O'BANION, M. KERRY · 1985 to 2023
$15.1M
Virology/Immunology CoreP30AI078498 · NIAID · UNIVERSITY OF ROCHESTER · PI DEWHURST, STEPHEN · 2008 to 2018
$14.6M
The T32 Predoctoral Training Program in Immunology (PTPI)T32AI007285 · NIAID · UNIVERSITY OF ROCHESTER · PI Scott Andrew Gerber, JACQUES Robert · 1986 to 2026
$7.6M
Training in Cellular, Biochemical and Molecular SciencesT32GM068411 · NIGMS · UNIVERSITY OF ROCHESTER · PI MAQUAT, LYNNE E · 2005 to 2019
$3.9M
Investigation of Latency Promoting Genes (LPGs) in HIV Oral Reservoir CellsR01DE025447 · NIDCR · UNIVERSITY OF ROCHESTER · PI ZHU, JIAN · 2015 to 2019
$1.9M
Role of FACT Proteins in Regulating HIV Transcription and LatencyR01GM117838 · NIGMS · UNIVERSITY OF ROCHESTER · PI ZHU, JIAN · 2015 to 2018
$1.2M
Cooperation of BRD4 and TAT Associated Proteins in HIV Transcription and LatencyR33AI116180 · NIAID · UNIVERSITY OF ROCHESTER · PI ZHU, JIAN · 2016 to 2018
$1.2M
NIAID NIH HHS P30 AI078498NIAID NIH HHS R33 AI116180NIAID NIH HHS T32 AI007285NIDCR NIH HHS R01 DE025447NIGMS NIH HHS R01 GM117838NIGMS NIH HHS T32 GM007356NIGMS NIH HHS T32 GM068411
6 · The paper itself

Abstract

A cure for human immunodeficiency virus type-1 (HIV-1) has been hampered by the limitation of current combination antiretroviral therapy (cART) to address the latent reservoirs in HIV-1 patients. One strategy proposed to eradicate these reservoirs is the "shock and kill" approach, where latency-reversing agents (LRAs) are used to reactivate and promote viral cell death and/or immune killing of reactivated cells. Here, we report that curaxin CBL0137, an antitumor compound, can potentiate tumor necrosis factor-α-mediated reactivation of latently infected HIV-1cell lines. Additionally, the single use of CBL0137 is sufficient to reactivate HIV-1 latent reservoirs in peripheral mononuclear cells (PBMCs) isolated from HIV-1 positive, cART-treated, aviremic patients. Thus, CBL0137 possesses capabilities as a LRA and could be considered for the "shock and kill" approach.

Indexed as

Virus LatencyCarbazolesCells, CulturedHIV-1HIV InfectionsHumansLeukocytes, MononuclearTumor Necrosis Factor-alphaVirus ActivationCarbazolesCBLC137Tumor Necrosis Factor-alphacuraxinsfacilitates chromatin transcription complexHIV-1 latencyhuman immunodeficiency virus type 1latency-reversing agents

Identifiers

PMID30989696
PMCPMC6599568

What OpenQuestion holds

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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.