Evidence map›Paper›PMID 37158107›Full record

ArticleCirculation2023

Polycomb Group Protein CBX7 Represses Cardiomyocyte Proliferation Through Modulation of the TARDBP/RBM38 Axis.

Kyu-Won Cho, Mark Andrade, Seongho Bae, Sangsung Kim, Jin Eyun Kim, Er Yearn Jang, Sangho Lee, Ahsan Husain, Roy L Sutliff, John W Calvert and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Circulation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
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  7. Review
  8. Article
  9. Sirt4 Deficiency Promotes Cardiomyocyte Proliferation and Cardiac Repair.Journal of cellular and molecular medicine · 2025
    Article
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  12. Article
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  16. Glycation in the cardiomyocyte.Vitamins and hormones · 2024
    Review
  17. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 2 institutions in 3 countries.

Kyu-Won ChoDivision of Cardiology (K.-W.C., M.A., S.B., S.K., J.E.K., E.Y.J., S.L., A.H., Y.-s.Y.), Emory University School of Medicine, Atlanta, GA.
Mark AndradeDivision of Cardiology (K.-W.C., M.A., S.B., S.K., J.E.K., E.Y.J., S.L., A.H., Y.-s.Y.), Emory University School of Medicine, Atlanta, GA.ORCID 0000-0002-5194-578X
Seongho BaeDivision of Cardiology (K.-W.C., M.A., S.B., S.K., J.E.K., E.Y.J., S.L., A.H., Y.-s.Y.), Emory University School of Medicine, Atlanta, GA.ORCID 0000-0002-3624-6649
Sangsung KimDivision of Cardiology (K.-W.C., M.A., S.B., S.K., J.E.K., E.Y.J., S.L., A.H., Y.-s.Y.), Emory University School of Medicine, Atlanta, GA.ORCID 0000-0001-9192-2614
Jin Eyun KimDivision of Cardiology (K.-W.C., M.A., S.B., S.K., J.E.K., E.Y.J., S.L., A.H., Y.-s.Y.), Emory University School of Medicine, Atlanta, GA.ORCID 0000-0002-6297-3292
Er Yearn JangDivision of Cardiology (K.-W.C., M.A., S.B., S.K., J.E.K., E.Y.J., S.L., A.H., Y.-s.Y.), Emory University School of Medicine, Atlanta, GA.
Sangho LeeDivision of Cardiology (K.-W.C., M.A., S.B., S.K., J.E.K., E.Y.J., S.L., A.H., Y.-s.Y.), Emory University School of Medicine, Atlanta, GA.ORCID 0000-0003-3771-7761
Ahsan HusainDivision of Cardiology (K.-W.C., M.A., S.B., S.K., J.E.K., E.Y.J., S.L., A.H., Y.-s.Y.), Emory University School of Medicine, Atlanta, GA.
Roy L SutliffDivision of Pulmonary, Allergy, Critical Care and Sleep Medicine (R.L.S.), Emory University School of Medicine, Atlanta, GA.
John W CalvertDepartment of Medicine, Division of Cardiothoracic Surgery, Department of Surgery, Carlyle Fraser Heart Center (J.W.C.), Emory University School of Medicine, Atlanta, GA.ORCID 0000-0001-6858-6042
Changwon ParkDepartment of Molecular and Cellular Physiology, Louisiana State University Health Science Center, Shreveport (C.P.).
Young-Sup YoonDivision of Cardiology (K.-W.C., M.A., S.B., S.K., J.E.K., E.Y.J., S.L., A.H., Y.-s.Y.), Emory University School of Medicine, Atlanta, GA.ORCID 0000-0003-0051-0935
Emory University · USLouisiana State University Health Sciences Center Shreveport · US

Funding

Mechanisms of ER71/ETV2-regulated VascularizationR01HL119291 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PARK, CHANGWON · 2013 to 2022
$3.2M
Vascular Regeneration with Direct Reprogramming and Engineering StrategiesR01HL157242 · NHLBI · EMORY UNIVERSITY · PI YOON, YOUNG-SUP · 2022 to 2025
$2.1M
Physiology and Biophysics of Cardiac Slo2.1 ChannelsR01HL103877 · NHLBI · UNIVERSITY OF UTAH · PI SANGUINETTI, MICHAEL CRAIG, ZAITSEV, ALEXEY V · 2011 to 2015
$2.1M
Vascular Regeneration with Human Pluripotent Stem Cell-derived Vascular Cells and Engineering ApproachesR01HL156008 · NHLBI · EMORY UNIVERSITY · PI YOON, YOUNG-SUP · 2022 to 2025
$2.0M
Cardiac Revascularization with Direct Reprogramming ApproachesR01HL150887 · NHLBI · EMORY UNIVERSITY · PI YOON, YOUNG-SUP · 2020 to 2023
$1.8M
Human iPSC-derived endothelial cells as Vascular TherapeuticsR33HL154116 · NHLBI · EMORY UNIVERSITY · PI YOON, YOUNG-SUP · 2022 to 2022
$546k
NHLBI NIH HHS R01 HL103877NHLBI NIH HHS R01 HL119291NHLBI NIH HHS R01 HL150887NHLBI NIH HHS R01 HL156008NHLBI NIH HHS R01 HL157242NHLBI NIH HHS R33 HL154116
6 · The paper itself

Abstract

backgroundShortly after birth, cardiomyocytes exit the cell cycle and cease proliferation. At present, the regulatory mechanisms for this loss of proliferative capacity are poorly understood. CBX7 (chromobox 7), a polycomb group (PcG) protein, regulates the cell cycle, but its role in cardiomyocyte proliferation is unknown.

methodsWe profiled CBX7 expression in the mouse hearts through quantitative real-time polymerase chain reaction, Western blotting, and immunohistochemistry. We overexpressed CBX7 in neonatal mouse cardiomyocytes through adenoviral transduction. We knocked down CBX7 by using constitutive and inducible conditional knockout mice (

resultsWe explored

conclusionsOur results demonstrate that CBX7 directs the cell cycle exit of cardiomyocytes during the postnatal period by regulating its downstream targets TARDBP and RBM38. This is the first study to demonstrate the role of CBX7 in regulation of cardiomyocyte proliferation, and CBX7 could be an important target for cardiac regeneration.

Indexed as

DNA-Binding ProteinsMyocytes, CardiacAnimalsAnimals, NewbornCell ProliferationMiceMice, KnockoutPolycomb-Group ProteinsPolycomb Repressive Complex 1RNA-Binding ProteinsCbx7 protein, mouseDNA-Binding ProteinsPolycomb-Group ProteinsPolycomb Repressive Complex 1Rbm38 protein, mouseRNA-Binding ProteinsTardbp protein, mouseCBX7 proteincell cyclecell proliferationguided tissue regenerationhumanmyocytes, cardiacpolycomb-group proteins

Identifiers

PMID37158107
PMCPMC10330362
OpenAlexW4375949575

What OpenQuestion holds

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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.