Evidence map›Paper›PMID 32746905›Full record

ArticleStem cell research & therapy2020

HGF and IL-10 expressing ALB::GFP reporter cells generated from iPSCs show robust anti-fibrotic property in acute fibrotic liver model.

Ja Sung Choi, In Sil Jeong, Young-Jin Park, Sung-Whan Kim

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2020. 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
1.3field-weighted citation impact, top 20% 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, 16 citations in OpenAlex.

  1. Cell reprogramming: methods, mechanisms and applications.Cell regeneration (London, England) · 2025
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Induced pluripotent stem cell-based therapies for organ fibrosis.Frontiers in bioengineering and biotechnology · 2023
    Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Cell-Based Regeneration and Treatment of Liver Diseases.International journal of molecular sciences · 2021
    Review
  12. Article
  13. Article
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

4 authors at 3 institutions in 1 country.

Ja Sung ChoiDepartment of Internal Medicine, Catholic Kwandong University College of Medicine, International St. Mary's Hospital, Incheon, Republic of Korea.
In Sil JeongDepartment Medicine, Catholic Kwandong University College of Medicine, Gangneung, Republic of Korea.
Young-Jin ParkDepartment of Family Medicine, Dong-A University College of Medicine, Dong-A University Medical Center, Busan, Republic of Korea.
Sung-Whan KimDepartment Medicine, Catholic Kwandong University College of Medicine, Gangneung, Republic of Korea. swkim@cku.ac.kr.ORCID 0000-0003-3616-144X
Catholic Kwandong University International St. Mary's Hospital · KRCatholic Kwandong University · KRDong-A University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCell therapy using hepatocytes derived from stem cells has been regarded as a promising alternate to liver transplantation. However, the heterogeneity of these hepatocytes makes them unsuitable for therapeutic use. To overcome this limitation, we generated homogenous hepatocyte like induced hepatocyte-like (iHep) cells.

methodsiHep cells were generated from induced pluripotent stem cells (iPSCs) integrated with the albumin (ALB) reporter gene. The therapeutic properties of these iHep cells were investigated after transplantation in fibrotic liver tissues of a mouse model.

resultsThe iHep cells expressed hepatocyte specific genes and proteins, and exhibited high levels of hepatocyte growth factor (HGF) and interleukin (IL)-10 expressions. Transplantation of iHep cells significantly decreased thioacetamide (TAA)-induced liver fibrosis, apoptotic cells in the liver, and ameliorated abnormal liver function. Liver tissues engrafted with iHep cells exhibited decreased expression of pro-inflammatory factors such as transforming growth factor (TGF)-β, IL-6, and monocyte chemo attractant protein (MCP)-1. Furthermore, an increased number of proliferating hepatocytes and human albumin-expressing iHep cells were detected in mice liver.

conclusionsThis study has investigated and proven the liver regeneration potential of genome-edited iHep cells and promises to be a strong foundation for further studies exploring cell therapy as an alternative therapeutic option for the treatment of liver fibrosis.

Indexed as

Gene EditingHepatocyte Growth FactorInduced Pluripotent Stem CellsInterleukin-10Liver RegenerationAlbuminsAnimalsGenes, ReporterHepatocytesHumansLiverLiver CirrhosisMiceAlbuminsHepatocyte Growth FactorHGF protein, humanInterleukin-10AlbuminCell therapyDifferentiationGene editingHepatocyteKnock-inLiver cirrhosisReporter systemStem cellTALEN

Identifiers

PMID32746905
PMCPMC7398392
OpenAlexW3047076157

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.