Evidence map›Paper›PMID 28007615›Full record

ReviewBiotechnology advances

Human iPSC-derived cardiomyocytes and tissue engineering strategies for disease modeling and drug screening.

Alec S T Smith, Jesse Macadangdang, Winnie Leung, Michael A Laflamme, Deok-Ho Kim

Open access · greenAbstract readReview
In one paragraph

Review in Biotechnology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed
7.7field-weighted citation impact, top 2% 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

78 citing papers in PubMed, 153 citations in OpenAlex.

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18 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 2 countries.

Alec S T SmithDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Jesse MacadangdangDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Winnie LeungDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA.
Michael A LaflammeToronto General Research Institute, McEwen Centre for Regenerative Medicine, University Health Network, Toronto, ON, Canada.
Deok-Ho KimDepartment of Bioengineering, University of Washington, Seattle, WA 98195, USA; Center for Cardiovascular Biology, University of Washington, Seattle, WA 98109, USA; Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA 98109, USA. Electronic address: deokho@uw.edu.
University of Washington · USUniversity Health Network · CA

Funding

EXPERIMENTAL PATHOLOGY OF CARDIOVASCULAR DISEASET32HL007312 · NHLBI · UNIVERSITY OF WASHINGTON · PI MAJESKY, MARK W., SCHWARTZ, STEPHEN MARK · 1985 to 2019
$11.8M
Bioengineering Cardiovascular Training GrantT32EB001650 · NIBIB · UNIVERSITY OF WASHINGTON · PI REGNIER, MICHAEL · 2004 to 2019
$3.6M
Integration and Arrhythmia Suppression with hESC-Derived Cardiomyocyte GraftsR01HL117991 · NHLBI · UNIVERSITY OF WASHINGTON · PI LAFLAMME, MICHAEL ALAN · 2013 to 2015
$1.2M
Injectable myocardial matrix-grapheme composite hydrogels for functional cardiac tissue engineeringR21EB020132 · NIBIB · UNIVERSITY OF WASHINGTON · PI KIM, DEOK-HO · 2016 to 2017
$435k
American Heart Association-American Stroke Association 13SDG14560076NHLBI NIH HHS R01 HL117991NHLBI NIH HHS T32 HL007312NIBIB NIH HHS R21 EB020132NIBIB NIH HHS T32 EB001650
6 · The paper itself

Abstract

Improved methodologies for modeling cardiac disease phenotypes and accurately screening the efficacy and toxicity of potential therapeutic compounds are actively being sought to advance drug development and improve disease modeling capabilities. To that end, much recent effort has been devoted to the development of novel engineered biomimetic cardiac tissue platforms that accurately recapitulate the structure and function of the human myocardium. Within the field of cardiac engineering, induced pluripotent stem cells (iPSCs) are an exciting tool that offer the potential to advance the current state of the art, as they are derived from somatic cells, enabling the development of personalized medical strategies and patient specific disease models. Here we review different aspects of iPSC-based cardiac engineering technologies. We highlight methods for producing iPSC-derived cardiomyocytes (iPSC-CMs) and discuss their application to compound efficacy/toxicity screening and in vitro modeling of prevalent cardiac diseases. Special attention is paid to the application of micro- and nano-engineering techniques for the development of novel iPSC-CM based platforms and their potential to advance current preclinical screening modalities.

Indexed as

Drug Evaluation, PreclinicalInduced Pluripotent Stem CellsModels, BiologicalMyocytes, CardiacTissue EngineeringHumansCardiac differentiationDisease modelingDrug screeningInduced pluripotent stem cellsTissue engineering

Identifiers

PMID28007615
PMCPMC5237393
OpenAlexW2564219428

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.