Evidence map›Paper›PMID 25980938›Full record

ReviewAdvanced drug delivery reviews2016

Human pluripotent stem cells: Prospects and challenges as a source of cardiomyocytes for in vitro modeling and cell-based cardiac repair.

Matthew E Hartman, Dao-Fu Dai, Michael A Laflamme

Abstract readReview
In one paragraph

Review in Advanced drug delivery reviews, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing 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

58 citing papers in PubMed.

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  20. Treatment of Oxidative Stress with Exosomes in Myocardial Ischemia.International journal of molecular sciences · 2021
    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

3 authors.

Matthew E HartmanDivision of Cardiology, Department of Medicine, USA; Department of Genome Sciences, USA; Institute for Stem Cell and Regenerative Medicine, USA; Center for Cardiovascular Biology, USA.
Dao-Fu DaiInstitute for Stem Cell and Regenerative Medicine, USA; Center for Cardiovascular Biology, USA; Department of Pathology, University of Washington, Seattle, WA, USA.
Michael A LaflammeInstitute for Stem Cell and Regenerative Medicine, USA; Center for Cardiovascular Biology, USA; Department of Pathology, University of Washington, Seattle, WA, USA. Electronic address: laflamme@u.washington.edu.

Funding

Vascularization and Growth of Human Myocardial GraftsP01HL094374 · NHLBI · UNIVERSITY OF WASHINGTON · PI MINAMI, ELINA · 2010 to 2014
$14.5M
A Comprehensive Catalog of Dnasel Hypersensitive SitesU54HG007010 · NHGRI · UNIVERSITY OF WASHINGTON · PI STAMATOYANNOPOULOS, JOHN A · 2012 to 2016
$12.4M
Engineered Cardiac Morphogenesis-Stem Cells and ScaffoldsR01HL064387 · NHLBI · UNIVERSITY OF WASHINGTON · PI RATNER, BUDDY D · 2006 to 2010
$10.2M
Expansion of cardiac and hematopoietic progenitors by Wnt and NotchU01HL100405 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI EPSTEIN, JONATHAN A., MORRISEY, EDWARD E · 2009 to 2015
$8.1M
Integration and Arrhythmia Suppression with hESC-Derived Cardiomyocyte GraftsR01HL117991 · NHLBI · UNIVERSITY OF WASHINGTON · PI LAFLAMME, MICHAEL ALAN · 2013 to 2015
$1.2M
NHGRI NIH HHS U54 HG007010NHGRI NIH HHS U54-HG007010NHLBI NIH HHS P01 HL094374NHLBI NIH HHS P01-HL094374NHLBI NIH HHS R01 HL064387NHLBI NIH HHS R01-HL064387NHLBI NIH HHS R01 HL117991NHLBI NIH HHS R01-HL117991NHLBI NIH HHS U01 HL100405NHLBI NIH HHS U01-HL100405
6 · The paper itself

Abstract

Human pluripotent stem cells (PSCs) represent an attractive source of cardiomyocytes with potential applications including disease modeling, drug discovery and safety screening, and novel cell-based cardiac therapies. Insights from embryology have contributed to the development of efficient, reliable methods capable of generating large quantities of human PSC-cardiomyocytes with cardiac purities ranging up to 90%. However, for human PSCs to meet their full potential, the field must identify methods to generate cardiomyocyte populations that are uniform in subtype (e.g. homogeneous ventricular cardiomyocytes) and have more mature structural and functional properties. For in vivo applications, cardiomyocyte production must be highly scalable and clinical grade, and we will need to overcome challenges including graft cell death, immune rejection, arrhythmogenesis, and tumorigenic potential. Here we discuss the types of human PSCs, commonly used methods to guide their differentiation into cardiomyocytes, the phenotype of the resultant cardiomyocytes, and the remaining obstacles to their successful translation.

Indexed as

Models, BiologicalAnimalsCell DifferentiationCell SeparationEmbryonic Stem CellsEndodermHeart DiseasesHumansMesodermMyocytes, CardiacPluripotent Stem CellsTissue EngineeringCardiac regenerationCardiac repairCardiovascular diseaseDisease modelingDrug discoveryEmbryonic stem cellsHeart failureInduced pluripotent stem cells

Identifiers

PMID25980938
PMCPMC4644514

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.