Evidence map›Paper›PMID 40227166›Full record

ArticleJournal of medicinal chemistry2025

Efficacy and Toxicity Analysis of Selective BET Bromodomain Inhibitors in Models of Inflammatory Liver Disease.

Luke C Doskey, Cole R Scholtz, Nora R Vail, Shalil Khanal, Amani L Lee, Sai Giridhar Sarma Kandanur, Zachariah J Hoell, Amelia M Huehls, Mohamed R Issa, Enis Kostallari and 5 more

Abstract read
In one paragraph

Article in Journal of medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
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

15 authors.

Luke C DoskeyDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota 55905, United States.
Cole R ScholtzDepartment of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Nora R VailDepartment of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Shalil KhanalDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota 55905, United States.
Amani L LeeDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota 55905, United States.
Sai Giridhar Sarma KandanurDepartment of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.ORCID 0000-0003-2761-4355
Zachariah J HoellDepartment of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.
Amelia M HuehlsMayo Clinic Comprehensive Cancer Center, Rochester, Minnesota 55905, United States.
Mohamed R IssaMayo Clinic Comprehensive Cancer Center, Rochester, Minnesota 55905, United States.ORCID 0009-0003-1251-9627
Enis KostallariDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota 55905, United States.
Sheng CaoDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota 55905, United States.
Joel M ReidMayo Clinic Comprehensive Cancer Center, Rochester, Minnesota 55905, United States.ORCID 0000-0003-2872-3123
Vijay H ShahDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota 55905, United States.
Harmeet MalhiDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota 55905, United States.
William C K PomerantzDepartment of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.ORCID 0000-0002-0163-4078

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Lila J. Rutten · 1985 to 2026
$151.3M
TRAINING FOR FUTURE BIOTECHNOLOGY DEVELOPMENTT32GM008347 · NIGMS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI SCHMIDT-DANNERT, CLAUDIA · 1990 to 2021
$11.0M
Chemical Probe Development for Epigenetic Complexes Enabled by Protein-Observed 19F NMRR35GM140837 · NIGMS · UNIVERSITY OF MINNESOTA · PI William Charles Krause Pomerantz · 2021 to 2026
$2.5M
NCI NIH HHS P30 CA015083NIGMS NIH HHS R35 GM140837NIGMS NIH HHS T32 GM008347
6 · The paper itself

Abstract

BET bromodomain inhibitors demonstrate significant promise as anti-inflammatory agents. However, clinical data demonstrated that nonselective BET bromodomain inhibitors led to significant dose-limiting toxicity in clinical settings. Here, we use three orally bioavailable inhibitors,

Indexed as

Anti-Inflammatory AgentsLiver DiseasesTranscription FactorsAnimalsBromodomain Containing ProteinsCell Cycle ProteinsDisease Models, AnimalHumansInflammationMaleMiceStructure-Activity RelationshipAnti-Inflammatory AgentsBRD4 protein, humanBromodomain Containing ProteinsCell Cycle ProteinsTranscription Factors

Identifiers

PMID40227166
PMCPMC12731298

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.