Evidence map›Paper›PMID 29398486›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2018

Hepatocyte Growth Factor Improves the Therapeutic Efficacy of Human Bone Marrow Mesenchymal Stem Cells via RAD51.

Eun Ju Lee, Injoo Hwang, Ji Yeon Lee, Jong Nam Park, Keun Cheon Kim, Gi-Hwan Kim, Chang-Mo Kang, Irene Kim, Seo-Yeon Lee, Hyo-Soo Kim

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

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  15. Mesenchymal Stromal Cells and Exosomes: Progress and Challenges.Frontiers in cell and developmental biology · 2020
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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

10 authors at 3 institutions in 1 country.

Eun Ju LeeBiomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.
Injoo HwangMolecular Medicine & Biopharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea.
Ji Yeon LeeMolecular Medicine & Biopharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea.
Jong Nam ParkMolecular Medicine & Biopharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea.
Keun Cheon KimMolecular Medicine & Biopharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea.
Gi-Hwan KimMolecular Medicine & Biopharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea.
Chang-Mo KangKorea Institute of Radiological & Medical Sciences, Seoul, Republic of Korea.
Irene KimMolecular Medicine & Biopharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea.
Seo-Yeon LeeBiomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.
Hyo-Soo KimDepartment of Internal Medicine, Seoul National University College of Medicine, Molecular Medicine & Biopharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea. Electronic address: hyosoo@snu.ac.kr.
Seoul National University · KRSeoul National University Hospital · KRKorea Institute of Radiological and Medical Sciences · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human embryonic stem cell-derived mesenchymal stem cells (hE-MSCs) have greater proliferative capacity than other human mesenchymal stem cells (hMSCs), suggesting that they may have wider applications in regenerative cellular therapy. In this study, to uncover the anti-senescence mechanism in hE-MSCs, we compared hE-MSCs with adult bone marrow (hBM-MSCs) and found that hepatocyte growth factor (HGF) was more abundantly expressed in hE-MSCs than in hBM-MSCs and that it induced the transcription of RAD51 and facilitated its SUMOylation at K70. RAD51 induction/modification by HGF not only increased telomere length but also increased mtDNA replication, leading to increased ATP generation. Moreover, HGF-treated hBM-MSCs showed significantly better therapeutic efficacy than naive hBM-MSCs. Together, the data suggest that the RAD51-mediated effects of HGF prevent hMSC senescence by promoting telomere lengthening and inducing mtDNA replication and function, which opens the prospect of developing novel therapies for liver disease.

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsCore Binding Factor Alpha 2 SubunitDisease Models, AnimalDNA DamageDNA, MitochondrialEmbryonic Stem CellsGene Expression RegulationHepatocyte Growth FactorHumansIkaros Transcription FactorLiverLiver CirrhosisMaleMesenchymal Stem CellsMiceCore Binding Factor Alpha 2 SubunitDNA, MitochondrialHepatocyte Growth FactorIkaros Transcription FactorRad51 RecombinaseZfpn1a1 protein, mousehepatocyte growth factorhuman MSCliver fibrosisRAD51

Identifiers

PMID29398486
PMCPMC5910662
OpenAlexW2779764173

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.