Evidence map›Paper›PMID 31360783›Full record

ArticleHeliyon2019

Effect of ascorbic acid on differentiation of human amniotic fluid mesenchymal stem cells into cardiomyocyte-like cells.

Runchana Markmee, Sirinda Aungsuchawan, Peraphan Pothacharoen, Waleephan Tancharoen, Suteera Narakornsak, Tanongsak Laowanitwattana, Kanokkan Bumroongkit, Chaniporn Puaninta, Nathaporn Pangjaidee

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

9 citing papers in PubMed, 9 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

Runchana MarkmeeDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Sirinda AungsuchawanDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Peraphan PothacharoenDepartment of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Waleephan TancharoenDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Suteera NarakornsakDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Tanongsak LaowanitwattanaDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Kanokkan BumroongkitDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Chaniporn PuanintaDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Nathaporn PangjaideeDepartment of Anatomy, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Chiang Mai University · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to evaluate the efficiency of ascorbic acid (AA) on cell viability, cytotoxicity and the effects on cardiomyogenic differentiation of the human amniotic fluid mesenchymal stem cells (hAF-MSCs). The results of methylthiazole tetrazolium (MTT) assay and cell apoptosis assay indicated that after 24, 48 and 72 h of treatment, AA had no effect on cells viability and cytotoxicity. After treating the hAF-MSCs with 5-azacytidine (5-aza) and a combination of AA and 5-aza, the alamar blue cells proliferation assay showed the normal growth characteristic similar to control group. Especially, the morphological changes were observed between day 0 and day 21, and it was revealed that the hAF-MSCs exhibited myotube-like morphology after 7 days of cell culturing. Moreover, the treatment with a combination of AA and 5-aza was able to up-regulate the cardiomyogenic specific gene levels, which are known to play an important role in cardiomyogenesis. This was specifically notable with the results of immunofluorescence and immunoenzymatic staining in the AA combined with 5-aza treatment group, the highest expression of cardiomyogenic specific proteins was revealed including for GATA4, cTnT, Cx43 and Nkx2.5. It could be concluded that AA may be a good alternative cardiomyogenic inducing factor for hAF-MSCs and may open new insights into future biomedical applications for a clinically treatment.

Indexed as

5-AzacytidineAscorbic acidBiological sciencesCardiomyocyte-like cellsCardiomyogenic differentiationCell biologyHuman amniotic fluid mesenchymal stem cellsStem cell research

Identifiers

PMID31360783
PMCPMC6639694
OpenAlexW2959112351

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.