Evidence map›Paper›PMID 30334384›Full record

ReviewKorean circulation journal2018

Cardiac Regeneration with Human Pluripotent Stem Cell-Derived Cardiomyocytes.

Misun Park, Young Sup Yoon

Open access · hybridAbstract readReview
In one paragraph

Review in Korean circulation journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Engineered combinatorial cell device for wound healing and bone regeneration.Frontiers in bioengineering and biotechnology · 2023
    Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Update on heart failure management and future directions.The Korean journal of internal medicine · 2019
    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

2 authors at 2 institutions in 2 countries.

Misun ParkBiomedical Science Institute, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-9858-4408
Young Sup YoonBiomedical Science Institute, Yonsei University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-0051-0935
Emory University · USYonsei University · KR

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Effects of reprogrammed and engineered MSCs on diabetic complicationsDP3DK108245 · NIDDK · EMORY UNIVERSITY · PI YOON, YOUNG-SUP · 2015 to 2016
$2.6M
Prohealing multifunctional endothelium nanomatrix coated stentR01HL125391 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI JUN, HO-WOOK · 2015 to 2019
$1.8M
Stem Cell-based therapy for LymphedemaR01HL127759 · NHLBI · EMORY UNIVERSITY · PI YOON, YOUNG-SUP · 2015 to 2018
$1.6M
Cardiac Regeneration with Bioengineered Human Stem CellsR01HL129511 · NHLBI · EMORY UNIVERSITY · PI YOON, YOUNG-SUP · 2016 to 2019
$1.6M
Ministry of Health and Welfare HI15C2782Ministry of Health and Welfare HI16C2211National Heart, Lung, and Blood Institute R01HL127759National Heart, Lung, and Blood Institute R01HL129511National Institute of Diabetes and Digestive and Kidney Diseases DP3-DK108245National Institutes of Health 1R01HL125391-01National Institutes of Health P30CA013148National Research Foundation of Korea 2015M3A9C6031514National Research Foundation of Korea 2018R1D1A1B07046955NCI NIH HHS P30 CA013148NHLBI NIH HHS R01 HL125391NHLBI NIH HHS R01 HL127759NHLBI NIH HHS R01 HL129511NIDDK NIH HHS DP3 DK108245
6 · The paper itself

Abstract

Embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs), which are collectively called pluripotent stem cells (PSCs), have emerged as a promising source for regenerative medicine. Particularly, human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) have shown robust potential for regenerating injured heart. Over the past two decades, protocols to differentiate hPSCs into CMs at high efficiency have been developed, opening the door for clinical application. Studies further demonstrated therapeutic effects of hPSC-CMs in small and large animal models and the underlying mechanisms of cardiac repair. However, gaps remain in explanations of the therapeutic effects of engrafted hPSC-CMs. In addition, bioengineering technologies improved survival and therapeutic effects of hPSC-CMs in vivo. While most of the original concerns associated with the use of hPSCs have been addressed, several issues remain to be resolved such as immaturity of transplanted cells, lack of electrical integration leading to arrhythmogenic risk, and tumorigenicity. Cell therapy with hPSC-CMs has shown great potential for biological therapy of injured heart; however, more studies are needed to ensure the therapeutic effects, underlying mechanisms, and safety, before this technology can be applied clinically.

Indexed as

BiomaterialsCardiomyocytesCell- and tissue-based therapyPluripotent stem cellsRegeneration

Identifiers

PMID30334384
PMCPMC6196153
OpenAlexW2896654287

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.