Evidence map›Paper›PMID 30089714›Full record

ArticleJCI insight2018

HDAC11 suppresses the thermogenic program of adipose tissue via BRD2.

Rushita A Bagchi, Bradley S Ferguson, Matthew S Stratton, Tianjing Hu, Maria A Cavasin, Lei Sun, Ying-Hsi Lin, Dianxin Liu, Pilar Londono, Kunhua Song and 7 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
5.7field-weighted citation impact, top 3% of its field
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

69 citing papers in PubMed, 106 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. HDAC11 Regulates RNA Splicing via De-Fatty Acylation of SF3B2.bioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Targeting Histone Deacetylase 11 with a Highly Selective Inhibitor for the Treatment of MASLD.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  17. Article
  18. Review
  19. Article
  20. Energy metabolism in health and diseases.Signal transduction and targeted therapy · 2025
    Review

9 more citing papers are in PubMed but not listed here.

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

17 authors at 5 institutions in 1 country.

Rushita A BagchiDepartment of Medicine, Division of Cardiology, and.
Bradley S FergusonDepartment of Medicine, Division of Cardiology, and.
Matthew S StrattonDepartment of Medicine, Division of Cardiology, and.
Tianjing HuDepartment of Medicine, Division of Cardiology, and.
Maria A CavasinDepartment of Medicine, Division of Cardiology, and.
Lei SunGeorge Washington University Cancer Center, Washington, DC, USA.
Ying-Hsi LinDepartment of Medicine, Division of Cardiology, and.
Dianxin LiuIntegrative Metabolism Program, Sanford Burnham Prebys Medical Discovery Institute, Orlando, Florida, USA.
Pilar LondonoDepartment of Medicine, Division of Cardiology, and.
Kunhua SongDepartment of Medicine, Division of Cardiology, and.
Maria F PinoTranslational Research Institute for Metabolism and Diabetes, Florida Hospital, Orlando, Florida, USA.
Lauren M SparksTranslational Research Institute for Metabolism and Diabetes, Florida Hospital, Orlando, Florida, USA.
Steven R SmithTranslational Research Institute for Metabolism and Diabetes, Florida Hospital, Orlando, Florida, USA.
Philipp E SchererTouchstone Diabetes Center, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Sheila CollinsIntegrative Metabolism Program, Sanford Burnham Prebys Medical Discovery Institute, Orlando, Florida, USA.
Edward SetoGeorge Washington University Cancer Center, Washington, DC, USA.
Timothy A McKinseyDepartment of Medicine, Division of Cardiology, and.
University of Colorado Anschutz Medical Campus · USTranslational Research Institute for Metabolism and Diabetes · USGeorge Washington University · USSanford Burnham Prebys Medical Discovery Institute · USThe University of Texas Southwestern Medical Center · US

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Edward L Melanson · 1995 to 2026
$32.6M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Regulation of Chromatin Signaling in Heart Failure by the BRD4 Bromodomain Protein.R01HL127240 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MCKINSEY, TIMOTHY, SRIVASTAVA, DEEPAK · 2015 to 2022
$6.4M
POSTGRADUATE TRAINING IN CARDIOVASCULAR RESEARCHT32HL007822 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI BUTTRICK, PETER N., LEINWAND, LESLIE ANNE · 1996 to 2023
$6.2M
Mechanisms for cell signaling in the control of cardiomyogenesisR01HL133230 · NHLBI · UNIVERSITY OF SOUTH FLORIDA · PI Kunhua Song · 2016 to 2026
$4.2M
Regulation of Cardiac Signaling by Class I Histone DeacetylasesR01HL116848 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MCKINSEY, TIMOTHY · 2013 to 2021
$3.1M
Natriuretic peptide receptors, adipose browning and energy expenditureR01DK103056 · NIDDK · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI COLLINS, SHEILA · 2014 to 2017
$1.7M
Isoform-Selective HDAC Inhibitors for Age-Associated Diastolic DysfunctionR21AG043822 · NIA · UNIVERSITY OF COLORADO DENVER · PI MCKINSEY, TIMOTHY · 2012 to 2013
$414k
Role of BET proteins in cardiac remodelingF32HL126354 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI STRATTON, MATTHEW · 2015 to 2015
$54k
NHLBI NIH HHS F32 HL126354NHLBI NIH HHS R01 HL116848NHLBI NIH HHS R01 HL127240NHLBI NIH HHS R01 HL133230NHLBI NIH HHS T32 HL007822NIA NIH HHS R21 AG043822NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R01 DK103056
6 · The paper itself

Abstract

Little is known about the biological function of histone deacetylase 11 (HDAC11), which is the lone class IV HDAC. Here, we demonstrate that deletion of HDAC11 in mice stimulates brown adipose tissue (BAT) formation and beiging of white adipose tissue (WAT). Consequently, HDAC11-deficient mice exhibit enhanced thermogenic potential and, in response to high-fat feeding, attenuated obesity, improved insulin sensitivity, and reduced hepatic steatosis. Ex vivo and cell-based assays revealed that HDAC11 catalytic activity suppresses the BAT transcriptional program, in both the basal state and in response to β-adrenergic receptor signaling, through a mechanism that is dependent on physical association with BRD2, a bromodomain and extraterminal (BET) acetyl-histone-binding protein. These findings define an epigenetic pathway for the regulation of energy homeostasis and suggest the potential for HDAC11-selective inhibitors for the treatment of obesity and diabetes.

Indexed as

Adipose Tissue, BrownAdipose Tissue, WhiteAdultAgedAged, 80 and overAnimalsBromodomain Containing ProteinsDiet, High-FatDisease Models, AnimalEnergy MetabolismEpigenesis, GeneticFatty LiverFemaleGene Expression RegulationHistone DeacetylasesHumansBRD2 protein, humanBrd2 protein, mouseBromodomain Containing ProteinsHDAC11 protein, humanHdac11 protein, mouseHistone DeacetylasesTranscription FactorsAdipose tissueMetabolismTranscription

Identifiers

PMID30089714
PMCPMC6129125
OpenAlexW2794856460

What OpenQuestion holds

Textmetadata
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.