Evidence map›Paper›PMID 26877613›Full record

ArticleWorld journal of gastroenterology2016

Human urokinase-type plasminogen activator gene-modified bone marrow-derived mesenchymal stem cells attenuate liver fibrosis in rats by down-regulating the Wnt signaling pathway.

Zhi-Gang Ma, Xiao-Dan Lv, Ling-Ling Zhan, Lan Chen, Qi-Yuan Zou, Ji-Qiao Xiang, Jiao-Li Qin, Wei-Wei Zhang, Zhao-Jing Zeng, Hui Jin and 2 more

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it, 31 citations in OpenAlex.

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  7. SimulatedPostepy dermatologii i alergologii · 2022
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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

12 authors at 1 institution in 1 country.

Zhi-Gang MaZhi-Gang Ma, Lan Chen, Qi-Yuan Zou, Ji-Qiao Xiang, Jiao-Li Qin, Wei-Wei Zhang, Zhao-Jing Zeng, Hui Jin, Hai-Xing Jiang, Xiao-Ping Lv, Department of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China.
Xiao-Dan LvZhi-Gang Ma, Lan Chen, Qi-Yuan Zou, Ji-Qiao Xiang, Jiao-Li Qin, Wei-Wei Zhang, Zhao-Jing Zeng, Hui Jin, Hai-Xing Jiang, Xiao-Ping Lv, Department of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China.
Ling-Ling ZhanZhi-Gang Ma, Lan Chen, Qi-Yuan Zou, Ji-Qiao Xiang, Jiao-Li Qin, Wei-Wei Zhang, Zhao-Jing Zeng, Hui Jin, Hai-Xing Jiang, Xiao-Ping Lv, Department of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China.
Lan ChenZhi-Gang Ma, Lan Chen, Qi-Yuan Zou, Ji-Qiao Xiang, Jiao-Li Qin, Wei-Wei Zhang, Zhao-Jing Zeng, Hui Jin, Hai-Xing Jiang, Xiao-Ping Lv, Department of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China.
Qi-Yuan ZouZhi-Gang Ma, Lan Chen, Qi-Yuan Zou, Ji-Qiao Xiang, Jiao-Li Qin, Wei-Wei Zhang, Zhao-Jing Zeng, Hui Jin, Hai-Xing Jiang, Xiao-Ping Lv, Department of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China.
Ji-Qiao XiangZhi-Gang Ma, Lan Chen, Qi-Yuan Zou, Ji-Qiao Xiang, Jiao-Li Qin, Wei-Wei Zhang, Zhao-Jing Zeng, Hui Jin, Hai-Xing Jiang, Xiao-Ping Lv, Department of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China.
Jiao-Li QinZhi-Gang Ma, Lan Chen, Qi-Yuan Zou, Ji-Qiao Xiang, Jiao-Li Qin, Wei-Wei Zhang, Zhao-Jing Zeng, Hui Jin, Hai-Xing Jiang, Xiao-Ping Lv, Department of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China.
Wei-Wei ZhangZhi-Gang Ma, Lan Chen, Qi-Yuan Zou, Ji-Qiao Xiang, Jiao-Li Qin, Wei-Wei Zhang, Zhao-Jing Zeng, Hui Jin, Hai-Xing Jiang, Xiao-Ping Lv, Department of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China.
Zhao-Jing ZengZhi-Gang Ma, Lan Chen, Qi-Yuan Zou, Ji-Qiao Xiang, Jiao-Li Qin, Wei-Wei Zhang, Zhao-Jing Zeng, Hui Jin, Hai-Xing Jiang, Xiao-Ping Lv, Department of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China.
Hui JinZhi-Gang Ma, Lan Chen, Qi-Yuan Zou, Ji-Qiao Xiang, Jiao-Li Qin, Wei-Wei Zhang, Zhao-Jing Zeng, Hui Jin, Hai-Xing Jiang, Xiao-Ping Lv, Department of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China.
Hai-Xing JiangZhi-Gang Ma, Lan Chen, Qi-Yuan Zou, Ji-Qiao Xiang, Jiao-Li Qin, Wei-Wei Zhang, Zhao-Jing Zeng, Hui Jin, Hai-Xing Jiang, Xiao-Ping Lv, Department of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China.
Xiao-Ping LvZhi-Gang Ma, Lan Chen, Qi-Yuan Zou, Ji-Qiao Xiang, Jiao-Li Qin, Wei-Wei Zhang, Zhao-Jing Zeng, Hui Jin, Hai-Xing Jiang, Xiao-Ping Lv, Department of Gastroenterology, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China.
Guangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo evaluate the therapeutic effects of bone marrow-derived mesenchymal stem cells (BMSCs) with human urokinase-type plasminogen activator (uPA) on liver fibrosis, and to investigate the mechanism of gene therapy.

methodsBMSCs transfected with adenovirus-mediated human urokinase plasminogen activator (Ad-uPA) were transplanted into rats with CCl4-induced liver fibrosis. All rats were sacrificed after 8 wk, and their serum and liver tissue were collected for biochemical, histopathologic, and molecular analyzes. The degree of liver fibrosis was assessed by hematoxylin and eosin or Masson's staining. Western blot and quantitative reverse transcription-polymerase chain reaction were used to determine protein and mRNA expression levels.

resultsSerum levels of alanine aminotransferase, aminotransferase, total bilirubin, hyaluronic acid, laminin, and procollagen type III were markedly decreased, whereas the levels of serum albumin were increased by uPA gene modified BMSCs treatment. Histopathology revealed that chronic CCl4-treatment resulted in significant fibrosis while uPA gene modified BMSCs treatment significantly reversed fibrosis. By quantitatively analysing the fibrosis area of liver tissue using Masson staining in different groups of animals, we found that model animals with CCl4-induced liver fibrosis had the largest fibrotic area (16.69% ± 1.30%), while fibrotic area was significantly decreased by BMSCs treatment (12.38% ± 2.27%) and was further reduced by uPA-BMSCs treatment (8.31% ± 1.21%). Both protein and mRNA expression of β-catenin, Wnt4 and Wnt5a was down-regulated in liver tissues following uPA gene modified BMSCs treatment when compared with the model animals.

conclusionTransplantation of uPA gene modified BMSCs suppressed liver fibrosis and ameliorated liver function and may be a new approach to treating liver fibrosis. Furthermore, treatment with uPA gene modified BMSCs also resulted in a decrease in expression of molecules of the Wnt signaling pathway.

Indexed as

Mesenchymal Stem Cell TransplantationWnt Signaling PathwayAdenoviridaeAnimalsbeta CateninCarbon TetrachlorideCells, CulturedChemical and Drug Induced Liver InjuryEnzyme InductionGenetic TherapyGenetic VectorsHumansLiverLiver Cirrhosis, ExperimentalMaleMesenchymal Stem Cellsbeta CateninCarbon TetrachlorideCtnnb1 protein, ratUrokinase-Type Plasminogen ActivatorWnt4 ProteinWnt4 protein, ratWnt-5a ProteinWnt5a protein, ratBone marrow-derived mesenchymal stem cellsLiver fibrosisUrokinase plasminogen activatorWnt signaling pathway

Identifiers

PMID26877613
PMCPMC4726681
OpenAlexW2420356353

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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.