Evidence map›Paper›PMID 29158523›Full record

ArticleScientific reports2017

Treatment of Myocardial Infarction with Gene-modified Mesenchymal Stem Cells in a Small Molecular Hydrogel.

Zhiye Wu, Guoqin Chen, Jianwu Zhang, Yongquan Hua, Jinliang Li, Bei Liu, Anqing Huang, Hekai Li, Minsheng Chen, Caiwen Ou

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

23 citing papers in PubMed, 48 citations in OpenAlex.

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  19. Increasing the Therapeutic Potential of Stem Cell Therapies for Critical Limb Ischemia.HSOA journal of stem cells research, development & therapy · 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.

Zhiye WuDepartment of Cardiology, Heart Center, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, China.
Guoqin ChenCardiovascular Medicine Department of Central Hospital of Panyu District, Guangzhou, 510280, China.
Jianwu ZhangDepartment of Cardiology, Nanfang Hospital, Southern Medical University, Guangzhou, 510515, China.
Yongquan HuaDepartment of Cardiology, Heart Center, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, China.
Jinliang LiCardiovascular Medicine Department of Central Hospital of Panyu District, Guangzhou, 510280, China.
Bei LiuDepartment of Cardiology, Shanghai general hospital, Shanghai, 200000, China.
Anqing HuangDepartment of Cardiology, Heart Center, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, China.
Hekai LiDepartment of Cardiology, Heart Center, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, China.
Minsheng ChenDepartment of Cardiology, Heart Center, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, China. gzminsheng@vip.163.com.
Caiwen OuDepartment of Cardiology, Heart Center, Zhujiang Hospital, Southern Medical University, Guangzhou, 510280, China. 1284572007@qq.com.
Southern Medical University · CNPanyu District Central Hospital · CNZhujiang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The effect of transplanted rat mesenchymal stem cells (MSCs) can be reduced by extracellular microenvironment in myocardial infarction (MI). We tested a novel small-molecular hydrogel (SMH) on whether it could provide a scaffold for hepatocyte growth factor (HGF)-modified MSCs and alleviate ventricular remodeling while preserving cardiac function after MI. Overexpression of HGF in MSCs increased Bcl-2 and reduced Bax and caspase-3 levels in response to hypoxia in vitro. Immunocytochemistry demonstrated that cardiac troponin (cTnT), desmin and connexin 43 expression were significantly enhanced in the 5-azacytidine (5-aza) with SMH group compared with the 5-aza only group in vitro and in vivo. Bioluminescent imaging indicated that retention and survival of transplanted cells was highest when MSCs transfected with adenovirus (ad-HGF) were injected with SMH. Heart function and structure improvement were confirmed by echocardiography and histology in the Ad-HGF-SMHs-MSCs group compared to other groups. Our study showed that: HGF alleviated cell apoptosis and promoted MSC growth. SMHs improved stem cell adhesion, survival and myocardial cell differentiation after MSC transplantation. SMHs combined with modified MSCs significantly decreased the scar area and improved cardiac function.

Indexed as

Mesenchymal Stem Cell TransplantationAdenoviridaeAnimalsbcl-2-Associated X ProteinCaspase 3Cell AdhesionCell DifferentiationDisease Models, AnimalGene Expression Regulation, DevelopmentalHeartHepatocyte Growth FactorHumansHydrogelsMesenchymal Stem CellsMyocardial InfarctionProto-Oncogene Proteins c-bcl-2bcl-2-Associated X ProteinBcl2 protein, ratCaspase 3Hepatocyte Growth FactorHGF protein, humanHydrogelsProto-Oncogene Proteins c-bcl-2

Identifiers

PMID29158523
PMCPMC5696474
OpenAlexW2770642954

What OpenQuestion holds

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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.