Evidence map›Paper›PMID 32120837›Full record

ArticleCells2020

Src Inhibition Attenuates Liver Fibrosis by Preventing Hepatic Stellate Cell Activation and Decreasing Connetive Tissue Growth Factor.

Hye-Young Seo, So-Hee Lee, Ji-Ha Lee, Yu Na Kang, Jae Seok Hwang, Keun-Gyu Park, Mi Kyung Kim, Byoung Kuk Jang

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
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  6. Review
  7. Chronic alcohol intake elicits distinct multi-omic profiles in the liverbioRxiv : the preprint server for biology · 2025
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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

8 authors at 2 institutions in 1 country.

Hye-Young SeoDepartment of Internal Medicine, Keimyung University School of Medicine, Daegu 42601, Korea.
So-Hee LeeDepartment of Internal Medicine, Keimyung University School of Medicine, Daegu 42601, Korea.
Ji-Ha LeeDepartment of Internal Medicine, Keimyung University School of Medicine, Daegu 42601, Korea.
Yu Na KangDepartment of Pathology, Keimyung University School of Medicine, Daegu 42601, Korea.
Jae Seok HwangDepartment of Internal Medicine, Keimyung University School of Medicine, Daegu 42601, Korea.
Keun-Gyu ParkDepartment of Internal Medicine, School of Medicine, Kyungpook National University, Daegu 41944, Korea.
Mi Kyung KimDepartment of Internal Medicine, Keimyung University School of Medicine, Daegu 42601, Korea.
Byoung Kuk JangDepartment of Internal Medicine, Keimyung University School of Medicine, Daegu 42601, Korea.
Keimyung University · KRKyungpook National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The SRC kinase family comprises non-receptor tyrosine kinases that are ubiquitously expressed in all cell types. Although Src is reportedly activated in pulmonary and renal fibrosis, little is known regarding its role in liver fibrosis. This study investigated whether the inhibition of Src protects against liver fibrosis. The expression of Src was upregulated in thioacetamide (TAA)-induced fibrotic mouse liver and cirrhosis of patients, and phospho-Src was upregulated during activation of hepatic stellate cells (HSC). In addition, Src inhibition reduced the expression of α-smooth muscle actin (αSMA) in primary HSCs and suppressed transforming growth factor β (TGF-β)-induced expression of connective tissue growth factor (CTGF) in hepatocytes. Src inhibitor Saracatinib also attenuated TAA-induced expression of type I collagen, αSMA, and CTGF in mouse liver tissues. The antifibrotic effect of Src inhibitors was associated with the downregulation of smad3, but not of signal transducer and activator of transcription 3 (STAT3). In addition, Src inhibition increased autophagy flux and protected against liver fibrosis. These results suggest that Src plays an important role in liver fibrosis and that Src inhibitors could be treat liver fibrosis.

Indexed as

AnimalsAutophagyBenzodioxolesCells, CulturedConnective Tissue Growth FactorHepatic Stellate CellsHumansLiver CirrhosisMaleMice, Inbred C57BLPhosphorylationQuinazolinessrc-Family KinasesSTAT3 Transcription FactorThioacetamideTransforming Growth Factor betaBenzodioxolesConnective Tissue Growth FactorQuinazolinessaracatinibsrc-Family KinasesSTAT3 Transcription FactorThioacetamideTransforming Growth Factor betaautophagyCTGFhepatocyteHSCliver fibrosisPP2saracatinibSmad3SrcTGF-β

Identifiers

PMID32120837
PMCPMC7140470
OpenAlexW3009302416

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.