Evidence map›Paper›PMID 30602218›Full record

ArticleGut and liver2019

The Use of Foxa2-Overexpressing Adipose Tissue-Derived Stem Cells in a Scaffold System Attenuates Acute Liver Injury.

Yeon Ji Chae, Dae Won Jun, Jai Sun Lee, Waqar Khalid Saeed, Hyeon Tae Kang, Kiseok Jang, Jin Ho Lee

Open access · diamondAbstract read
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Article in Gut and liver, 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
1.0field-weighted citation impact, top 24% 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, 15 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

7 authors at 2 institutions in 1 country.

Yeon Ji ChaeDepartment of Translational Medicine, Hanyang University Graduate School of Biomedical Science and Engineering, Seoul, Korea.ORCID http://orcid.org/0000-0001-8609-7082
Dae Won JunDepartment of Translational Medicine, Hanyang University Graduate School of Biomedical Science and Engineering, Seoul, Korea.ORCID http://orcid.org/0000-0002-2875-6139
Jai Sun LeeDepartment of Translational Medicine, Hanyang University Graduate School of Biomedical Science and Engineering, Seoul, Korea.ORCID http://orcid.org/0000-0002-1673-8777
Waqar Khalid SaeedDepartments of Internal Medicine, Hanyang University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0002-7888-9108
Hyeon Tae KangDepartment of Translational Medicine, Hanyang University Graduate School of Biomedical Science and Engineering, Seoul, Korea.ORCID http://orcid.org/0000-0002-4771-3388
Kiseok JangDepartments of Pathology, Hanyang University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0002-6585-3990
Jin Ho LeeDepartment of Advanced Materials, Hannam University, Daejeon, Korea.ORCID http://orcid.org/0000-0002-1528-3416
Hanyang University · KRHannam University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/Aims: For the clinical application of stem cell therapy, functional enhancement is needed to increase the survival rate and the engraftment rate. The purpose of this study was to investigate functional enhancement of the paracrine effect using stem cells and hepatocyte-like cells and to minimize stem cell homing by using a scaffold system in a liver disease model. Methods: A microporator was used to overexpress Foxa2 in adipose tissue-derived stem cells (ADSCs), which were cultured in a poly(lactic-co-glycolic acid) (PLGA) scaffold. Later, the ADSCs were cultured in hepatic differentiation medium for 2 weeks by a 3-step method. For Results: Foxa2-overexpressing ADSCs showed greater increases in hepatocyte-specific gene markers (alpha fetoprotein [AFP], cytokeratin 18 [CK18], and albumin), cytoplasmic glycogen storage, and cytochrome P450 expression than cells that underwent the conventional differentiation method. Conclusions: Foxa2-overexpressing ADSCs applied in a scaffold system enhanced hepatocyte-like differentiation and attenuated acute liver damage in an acute liver injury model without homing effects.

Indexed as

Tissue ScaffoldsAlbuminsalpha-FetoproteinsAnimalsBiocompatible MaterialsCell DifferentiationCells, CulturedChemical and Drug Induced Liver InjuryConnexinsCytochrome P-450 Enzyme SystemDipeptidyl Peptidase 4ElectroporationGap Junction beta-1 ProteinGlycogenHepatocyte Nuclear Factor 3-betaHepatocytesAlbuminsalpha-FetoproteinsBiocompatible MaterialsConnexinsCytochrome P-450 Enzyme SystemDipeptidyl Peptidase 4Gap Junction beta-1 ProteinGlycogenHepatocyte Nuclear Factor 3-betaKeratin-18Polylactic Acid-Polyglycolic Acid CopolymerThioacetamideacuteFoxa2Liver failureMesenchymal stem cellScaffold

Identifiers

PMID30602218
PMCPMC6622567
OpenAlexW2907263806

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.