Evidence map›Paper›PMID 37744352›Full record

ArticleFrontiers in immunology2023

Elucidating the direct effects of the novel HDAC inhibitor bocodepsin (OKI-179) on T cells to rationally design regimens for combining with immunotherapy.

Nisha Holay, Alexander Somma, Mark Duchow, Milad Soleimani, Anna Capasso, Srividya Kottapalli, Joshua Rios, Uma Giri, Jennifer Diamond, Anna Schreiber and 4 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

14 authors.

Nisha HolayInterdisciplinary Life Sciences Graduate Programs, The University of Texas at Austin, Austin, TX, United States.
Alexander SommaLivestrong Cancer Institutes, Department of Oncology, Dell Medical School, The University of Texas at Austin, Austin, TX, United States.
Mark DuchowLivestrong Cancer Institutes, Department of Oncology, Dell Medical School, The University of Texas at Austin, Austin, TX, United States.
Milad SoleimaniInterdisciplinary Life Sciences Graduate Programs, The University of Texas at Austin, Austin, TX, United States.
Anna CapassoLivestrong Cancer Institutes, Department of Oncology, Dell Medical School, The University of Texas at Austin, Austin, TX, United States.
Srividya KottapalliLivestrong Cancer Institutes, Department of Oncology, Dell Medical School, The University of Texas at Austin, Austin, TX, United States.
Joshua RiosLivestrong Cancer Institutes, Department of Oncology, Dell Medical School, The University of Texas at Austin, Austin, TX, United States.
Uma GiriLivestrong Cancer Institutes, Department of Oncology, Dell Medical School, The University of Texas at Austin, Austin, TX, United States.
Jennifer DiamondOnKure Therapeutics, Boulder, CO, United States.
Anna SchreiberUniversity of Colorado Cancer Center, University of Colorado Anschutz Medical Campus, Denver, CO, United States.
Anthony D PiscopioOnKure Therapeutics, Boulder, CO, United States.
Carla Van Den BergInterdisciplinary Life Sciences Graduate Programs, The University of Texas at Austin, Austin, TX, United States.
S Gail EckhardtInterdisciplinary Life Sciences Graduate Programs, The University of Texas at Austin, Austin, TX, United States.
Todd A TriplettLivestrong Cancer Institutes, Department of Oncology, Dell Medical School, The University of Texas at Austin, Austin, TX, United States.

Funding

Porosity and tensioning: Critical factors to consider when choosing a prolapse meshR01HD083383 · NICHD · MAGEE-WOMEN'S RES INST AND FOUNDATION · PI ABRAMOWITCH, STEVEN D, MOALLI, PAMELA A. · 2016 to 2025
$5.5M
NICHD NIH HHS R01 HD083383
6 · The paper itself

Abstract

Histone deacetylase inhibitors (HDACi) are currently being explored for the treatment of both solid and hematological malignancies. Although originally thought to exert cytotoxic responses through tumor-intrinsic mechanisms by increasing expression of tumor suppressor genes, several studies have demonstrated that therapeutic responses depend on an intact adaptive immune system: particularly CD8 T cells. It is therefore critical to understand how HDACi directly affects T cells in order to rationally design regimens for combining with immunotherapy. In this study, we evaluated T cell responses to a novel class-selective HDACi (OKI-179, bocodepsin) by assessing histone acetylation levels, which revealed rapid responsiveness accompanied by an increase in CD4 and CD8 T cell frequencies in the blood. However, these rapid responses were transient, as histone acetylation and frequencies waned within 24 hours. This contrasts with

Indexed as

Histone Deacetylase InhibitorsHistonesCD8-Positive T-LymphocytesClinical ProtocolsHumansImmunotherapyHistone Deacetylase InhibitorsHistonescancercolorectal cancerHDACHDAC inhibitorsimmunologyimmunotherapyT cell

Identifiers

PMID37744352
PMCPMC10513502

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.