Evidence map›Paper›PMID 39586652›Full record

ReviewCurrent opinion in genetics & development2024

Control of cell fate upon transcription factor-driven cardiac reprogramming.

Huitong Shi, Brian M Spurlock, Jiandong Liu, Li Qian

Abstract readReview
In one paragraph

Review in Current opinion in genetics & development, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. [Systemic Reprogramming of Cellular Senescence: Coordinated Regulation of Metabolism, Epigenetics, and Proteostasis].Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition · 2026
    Review
  2. 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

4 authors.

Huitong ShiThe McAllister Heart Institute, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; Department of Pathology and Laboratory Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Brian M SpurlockThe McAllister Heart Institute, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; Department of Pathology and Laboratory Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA. Electronic address: https://twitter.com/@brineshrimp2.
Jiandong LiuThe McAllister Heart Institute, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; Department of Pathology and Laboratory Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Li QianThe McAllister Heart Institute, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA; Department of Pathology and Laboratory Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA. Electronic address: li_qian@med.unc.edu.

Funding

Altering Cardiac Cell Fate for Heart RepairR35HL155656 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Li Qian · 2021 to 2026
$5.5M
Macrophage functional dynamics in adult heart regenerationR01HL164933 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Jiandong Liu · 2023 to 2026
$2.4M
The role of RNA-binding protein Lin28a in hypertrophic cardiomyopathyR01HL139976 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIU, JIANDONG · 2019 to 2022
$2.1M
Molecular regulation of ventricular chamber maturationR01HL139880 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIU, JIANDONG · 2018 to 2022
$2.0M
Role of RBP in programming and reprogramming of cardiac fibroblastsR01HL174774 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Jiandong Liu · 2024 to 2026
$2.0M
Studying Mitochondrial Dynamics and Energetics During Cardiac ReprogrammingF32HL176045 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SPURLOCK, BRIAN M · 2024 to 2025
$162k
American Heart Association-American Stroke Association 24POST1199447NHLBI NIH HHS F32 HL176045NHLBI NIH HHS R01 HL139880NHLBI NIH HHS R01 HL139976NHLBI NIH HHS R01 HL164933NHLBI NIH HHS R01 HL174774NHLBI NIH HHS R35 HL155656
6 · The paper itself

Abstract

Adult mammals are susceptible to substantial cardiomyocyte (CM) loss following various cardiac diseases due to the limited capacity of CM proliferation and regeneration. Recently, direct cardiac reprogramming, converting fibroblasts into induced CMs, has been achieved both in vitro and in vivo through forced expression of transcription factors (TFs). This review encapsulates the advancements made in enhancing reprogramming efficiency and underlying molecular mechanisms. It covers the optimization of TF-based reprogramming cocktails and in vivo delivery platform and recently identified regulators in enhancing reprogramming efficiency. In addition, we discuss recent insights into the molecular mechanisms of direct cardiac reprogramming from single-cell omics analyses. Finally, we briefly touch on remaining challenges and prospective direction of this field.

Indexed as

Cellular ReprogrammingMyocytes, CardiacTranscription FactorsAnimalsCell DifferentiationFibroblastsHumansTranscription Factors

Identifiers

PMID39586652
PMCPMC11894758

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.