Evidence map›Paper›PMID 34657219›Full record

ReviewArchives of toxicology2021

Recent progress of iPSC technology in cardiac diseases.

Shunsuke Funakoshi, Yoshinori Yoshida

Abstract readReview
In one paragraph

Review in Archives of toxicology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
–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

24 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  15. Overcoming the challenges of scalable iPSC generation in translation medicine.Journal of the Chinese Medical Association : JCMA · 2024
    Article
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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

2 authors.

Shunsuke FunakoshiCenter for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan.
Yoshinori YoshidaCenter for iPS Cell Research and Application, Kyoto University, Kyoto, 606-8507, Japan. yoshinor@cira.kyoto-u.ac.jp.ORCID http://orcid.org/0000-0001-5511-9090

Funding

Fondation Leducq 18CVD05Japan Agency for Medical Research and Development JP19bk0104095Japan Agency for Medical Research and Development JP19bm0104001Japan Agency for Medical Research and Development JP19bm0204003Japan Agency for Medical Research and Development JP19bm0804008Japan Agency for Medical Research and Development JP19mk0104117Japan Agency for Medical Research and Development JP20bm0804022Japan Society for the Promotion of Science 17H04176Japan Society for the Promotion of Science 21H02912
6 · The paper itself

Abstract

It has been nearly 15 years since the discovery of human-induced pluripotent stem cells (iPSCs). During this time, differentiation methods to targeted cells have dramatically improved, and many types of cells in the human body can be currently generated at high efficiency. In the cardiovascular field, the ability to generate human cardiomyocytes in vitro with the same genetic background as patients has provided a great opportunity to investigate human cardiovascular diseases at the cellular level to clarify the molecular mechanisms underlying the diseases and discover potential therapeutics. Additionally, iPSC-derived cardiomyocytes have provided a powerful platform to study drug-induced cardiotoxicity and identify patients at high risk for the cardiotoxicity; thus, accelerating personalized precision medicine. Moreover, iPSC-derived cardiomyocytes can be sources for cardiac cell therapy. Here, we review these achievements and discuss potential improvements for the future application of iPSC technology in cardiovascular diseases.

Indexed as

AnimalsCardiotoxicityCardiovascular DiseasesCell- and Tissue-Based TherapyCell DifferentiationHumansInduced Pluripotent Stem CellsMyocytes, CardiacTechnologyCardiomyocyteDifferentiation into subtypesDisease modelingInduced pluripotent stem cellsMaturation

Identifiers

PMID34657219
PMCPMC8522114

What OpenQuestion holds

Textmetadata
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.