Evidence map›Paper›PMID 35722872›Full record

ArticleCirculation research2022

Epicardial HDAC3 Promotes Myocardial Growth Through a Novel MicroRNA Pathway.

Jihyun Jang, Guang Song, Sarah M Pettit, Qinshan Li, Xiaosu Song, Chen-Leng Cai, Sunjay Kaushal, Deqiang Li

Open access · bronzeAbstract read
In one paragraph

Article in Circulation research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 38 citations in OpenAlex.

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  10. mExperimental & molecular medicine · 2025
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  17. Epicardium-myocardium crosstalk orchestrates heart development.Frontiers in cell and developmental biology · 2025
    Review
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  19. Epicardial EMT and cardiac repair: an update.Stem cell research & therapy · 2024
    Review
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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

8 authors at 3 institutions in 1 country.

Jihyun JangCenter for Vascular and Inflammation Diseases (J.J., G.S., S.M.P., Q.L., X.S., D.L.), University of Maryland School of Medicine, Baltimore' MD.ORCID 0000-0002-4548-2037
Guang SongCenter for Vascular and Inflammation Diseases (J.J., G.S., S.M.P., Q.L., X.S., D.L.), University of Maryland School of Medicine, Baltimore' MD.ORCID 0000-0002-5459-6247
Sarah M PettitCenter for Vascular and Inflammation Diseases (J.J., G.S., S.M.P., Q.L., X.S., D.L.), University of Maryland School of Medicine, Baltimore' MD.
Qinshan LiCenter for Vascular and Inflammation Diseases (J.J., G.S., S.M.P., Q.L., X.S., D.L.), University of Maryland School of Medicine, Baltimore' MD.
Xiaosu SongCenter for Vascular and Inflammation Diseases (J.J., G.S., S.M.P., Q.L., X.S., D.L.), University of Maryland School of Medicine, Baltimore' MD.
Chen-Leng CaiDepartment of Pediatrics, Herman Wells Center for Pediatric Research, Indiana University School of Medicine, Indianapolis' IN (C.-l.C.).ORCID 0000-0001-6900-4737
Sunjay KaushalDivision of Cardiovascular-Thoracic Surgery, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago' IL (S.K.).
Deqiang LiCenter for Vascular and Inflammation Diseases (J.J., G.S., S.M.P., Q.L., X.S., D.L.), University of Maryland School of Medicine, Baltimore' MD.ORCID 0000-0002-4603-2855
University of Maryland, Baltimore · USIndiana University – Purdue University Indianapolis · USLurie Children's Hospital · US

Funding

Cardiac regeneration by histone deacetylasesR01HL153406 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI LI, DEQIANG · 2020 to 2024
$1.9M
Deciphering the mechanisms of c-kit+ cells in heart repairR01HL137036 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI SHOU, WEINIAN · 2018 to 2021
$1.6M
NHLBI NIH HHS R01 HL137036NHLBI NIH HHS R01 HL153406
6 · The paper itself

Abstract

backgroundEstablishment of the myocardial wall requires proper growth cues from nonmyocardial tissues. During heart development, the epicardium and epicardium-derived cells instruct myocardial growth by secreting essential factors including FGF (fibroblast growth factor) 9 and IGF (insulin-like growth factor) 2. However, it is poorly understood how the epicardial secreted factors are regulated, in particular by chromatin modifications for myocardial formation. The current study is to investigate whether and how HDAC (histone deacetylase) 3 in the developing epicardium regulates myocardial growth.

methodsVarious cellular and mouse models in conjunction with biochemical and molecular tools were employed to study the role of HDAC3 in the developing epicardium.

resultsWe deleted

conclusionsOur findings reveal a critical signaling pathway in which epicardial HDAC3 promotes compact myocardial growth by stimulating FGF9 and IGF2 through repressing miR-322 or miR-503, providing novel insights in elucidating the etiology of congenital heart defects and conceptual strategies to promote myocardial regeneration.

Indexed as

MicroRNAsAnimalsHeartMiceMyocardiumMyocytes, CardiacPericardiumSignal TransductionMicroRNAschromatincuesfetal heartpericardiumtranscriptome

Identifiers

PMID35722872
PMCPMC9308743
OpenAlexW4283164605

What OpenQuestion holds

Textmetadata
LicenceTDM
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.