Evidence map›Paper›PMID 33015415›Full record

ArticleJACC. Basic to translational science2020

Blockade of Fibroblast YAP Attenuates Cardiac Fibrosis and Dysfunction Through MRTF-A Inhibition.

Jamie Francisco, Yu Zhang, Jae Im Jeong, Wataru Mizushima, Shohei Ikeda, Andreas Ivessa, Shinichi Oka, Peiyong Zhai, Michelle D Tallquist, Dominic P Del Re

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in JACC. Basic to translational science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 103 papers.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed
8.3field-weighted citation impact, top 1% 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

103 citing papers in PubMed, 122 citations in OpenAlex.

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  14. Mechanical interplay between adipose tissues and disease progression.Bioengineering & translational medicine · 2026
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43 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 1 country.

Jamie FranciscoDepartment of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers New Jersey Medical School, Newark, New Jersey.
Yu ZhangDepartment of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers New Jersey Medical School, Newark, New Jersey.
Jae Im JeongDepartment of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers New Jersey Medical School, Newark, New Jersey.
Wataru MizushimaDepartment of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers New Jersey Medical School, Newark, New Jersey.
Shohei IkedaDepartment of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers New Jersey Medical School, Newark, New Jersey.
Andreas IvessaDepartment of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers New Jersey Medical School, Newark, New Jersey.
Shinichi OkaDepartment of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers New Jersey Medical School, Newark, New Jersey.
Peiyong ZhaiDepartment of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers New Jersey Medical School, Newark, New Jersey.
Michelle D TallquistCenter for Cardiovascular Research, John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu, Hawaii.
Dominic P Del ReDepartment of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers New Jersey Medical School, Newark, New Jersey.
Rutgers, The State University of New Jersey · USRutgers New Jersey Medical SchoolUniversity of Hawaiʻi at Mānoa · US

Funding

Regulation of cardiac inflammation by fibroblastsR01HL144067 · NHLBI · UNIVERSITY OF HAWAII AT MANOA · PI TALLQUIST, MICHELLE D · 2018 to 2021
$2.3M
The role of NF2 in myocardial ischemia and reperfusion injuryR01HL127339 · NHLBI · RBHS-NEW JERSEY MEDICAL SCHOOL · PI DEL RE, DOMINIC P · 2015 to 2019
$2.0M
The effect of myocardial inflammation on stem cell effectiveness as “repair cell” therapyR15HL135726 · NHLBI · NEW JERSEY INSTITUTE OF TECHNOLOGY · PI LEE, EUN JUNG ALICE · 2017 to 2017
$434k
NHLBI NIH HHS R01 HL127339NHLBI NIH HHS R01 HL144067NHLBI NIH HHS R15 HL135726
6 · The paper itself

Abstract

Fibrotic remodeling of the heart in response to injury contributes to heart failure, yet therapies to treat fibrosis remain elusive. Yes-associated protein (YAP) is activated in cardiac fibroblasts by myocardial infarction, and genetic inhibition of fibroblast YAP attenuates myocardial infarction-induced cardiac dysfunction and fibrosis. YAP promotes myofibroblast differentiation and associated extracellular matrix gene expression through engagement of TEA domain transcription factor 1 and subsequent de novo expression of myocardin-related transcription factor A. Thus, fibroblast YAP is a promising therapeutic target to prevent fibrotic remodeling and heart failure.

Indexed as

AngII, angiotensin IIcardiac fibrosisheart failureHippo signalingMCM, Mer-Cre-MerMI, myocardial infarctionMkl1, megakaryoblastic leukemia 1mRNA, messenger ribonucleic acidMRTF-A, myocardin-related transcription factor Amyocardial infarctionNRCF, neonatal rat cardiac fibroblastPDGFR, platelet-derived growth factor receptorPE, phenylephrineSMA, smooth muscle actinTEAD, TEA domain transcription factorTGF, transforming growth factorYAPYAP, yes-associated protein

Identifiers

PMID33015415
PMCPMC7524792
OpenAlexW3091295206

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.