Evidence map›Paper›PMID 35842576›Full record

ArticleMolecular medicine (Cambridge, Mass.)2022

Recombinant truncated latency-associated peptide alleviates liver fibrosis in vitro and in vivo via inhibition of TGF-β/Smad pathway.

Xudong Song, Jiayi Shi, Jieting Liu, Yong Liu, Yang Yu, Yufei Qiu, Zhiqin Cao, Yu Pan, Xiaohuan Yuan, Yanhui Chu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Molecular medicine (Cambridge, Mass.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.4field-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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Effect ofFrontiers in pharmacology · 2022
    Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
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  11. Antioxidant therapy against TGF-β/SMAD pathway involved in organ fibrosis.Journal of cellular and molecular medicine · 2024
    Review
  12. Article
  13. Article
  14. Impact of the transforming growth factor-β pathway on vascular restenosis and its mechanism.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2023
    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

11 authors at 1 institution in 1 country.

Xudong SongHeilongjiang Province Key Laboratory of Anti-Fibrosis Biotherapy, Mudanjiang Medical University, No. 3, Tongxiang Street, Aimin District, Mudanjiang, 157011, Heilongjiang, China.
Jiayi ShiHeilongjiang Province Key Laboratory of Anti-Fibrosis Biotherapy, Mudanjiang Medical University, No. 3, Tongxiang Street, Aimin District, Mudanjiang, 157011, Heilongjiang, China.
Jieting LiuHeilongjiang Province Key Laboratory of Anti-Fibrosis Biotherapy, Mudanjiang Medical University, No. 3, Tongxiang Street, Aimin District, Mudanjiang, 157011, Heilongjiang, China.
Yong LiuHeilongjiang Province Key Laboratory of Anti-Fibrosis Biotherapy, Mudanjiang Medical University, No. 3, Tongxiang Street, Aimin District, Mudanjiang, 157011, Heilongjiang, China.
Yang YuHeilongjiang Province Key Laboratory of Anti-Fibrosis Biotherapy, Mudanjiang Medical University, No. 3, Tongxiang Street, Aimin District, Mudanjiang, 157011, Heilongjiang, China.
Yufei QiuHeilongjiang Province Key Laboratory of Anti-Fibrosis Biotherapy, Mudanjiang Medical University, No. 3, Tongxiang Street, Aimin District, Mudanjiang, 157011, Heilongjiang, China.
Zhiqin CaoHeilongjiang Province Key Laboratory of Anti-Fibrosis Biotherapy, Mudanjiang Medical University, No. 3, Tongxiang Street, Aimin District, Mudanjiang, 157011, Heilongjiang, China.
Yu PanHeilongjiang Province Key Laboratory of Anti-Fibrosis Biotherapy, Mudanjiang Medical University, No. 3, Tongxiang Street, Aimin District, Mudanjiang, 157011, Heilongjiang, China.
Xiaohuan YuanHeilongjiang Province Key Laboratory of Anti-Fibrosis Biotherapy, Mudanjiang Medical University, No. 3, Tongxiang Street, Aimin District, Mudanjiang, 157011, Heilongjiang, China.
Yanhui ChuHeilongjiang Province Key Laboratory of Anti-Fibrosis Biotherapy, Mudanjiang Medical University, No. 3, Tongxiang Street, Aimin District, Mudanjiang, 157011, Heilongjiang, China. chuyanhui@mdjmu.edu.cn.
Dan WuHeilongjiang Province Key Laboratory of Anti-Fibrosis Biotherapy, Mudanjiang Medical University, No. 3, Tongxiang Street, Aimin District, Mudanjiang, 157011, Heilongjiang, China. wudan@mdjmu.edu.cn.ORCID 0000-0002-0241-4691
Mudanjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLiver fibrosis is a progressive liver injury response. Transforming growth factor β1 (TGF-β1) is oversecreted during liver fibrosis and promotes the development of liver fibrosis. Therapeutic approaches targeting TGF-β1 and its downstream pathways are essential to inhibit liver fibrosis. The N-terminal latency-associated peptide (LAP) blocks the binding of TGF-β1 to its receptor. Removal of LAP is critical for the activation of TGF-β1. Therefore, inhibition of TGF-β1 and its downstream pathways by LAP may be a potential approach to affect liver fibrosis.

methodsTruncated LAP (tLAP) plasmids were constructed. Recombinant proteins were purified by Ni affinity chromatography. The effects of LAP and tLAP on liver fibrosis were investigated in TGF-β1-induced HSC-T6 cells, AML12 cells and CCl

resultsLAP and tLAP could inhibit TGF-β1-induced AML12 cells inflammation, apoptosis and EMT, and could inhibit TGF-β1-induced HSC-T6 cells proliferation and fibrosis. LAP and tLAP could attenuate the pathological changes of liver fibrosis and inhibit the expression of fibrosis-related proteins and mRNAs in CCl

conclusionLAP and tLAP could alleviate liver fibrosis in vitro and in vivo via inhibition of TGF-β/Smad pathway. TLAP has higher expression level and more effective anti-fibrosis activity compared to LAP. This study may provide new ideas for the treatment of liver fibrosis.

Indexed as

Transforming Growth Factor betaTransforming Growth Factor beta1AnimalsHepatic Stellate CellsLiver CirrhosisMiceRecombinant ProteinsSignal TransductionSmad ProteinsRecombinant ProteinsSmad ProteinsTransforming Growth Factor betaTransforming Growth Factor beta1Latency-associated peptideLiver fibrosisTGF-β/Smad pathwayTransforming growth factor β1

Identifiers

PMID35842576
PMCPMC9288003
OpenAlexW4285587108

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.