Evidence map›Paper›PMID 34714484›Full record

ArticleMolecular biology reports2021

Saikosaponin-d alleviates hepatic fibrosis through regulating GPER1/autophagy signaling.

Yirong Chen, Renye Que, Na Zhang, Liubing Lin, Mengen Zhou, Yong Li

Open access · hybridAbstract read
In one paragraph

Article in Molecular biology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-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

10 citing papers in PubMed, 23 citations in OpenAlex.

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  8. GPCRs and fibroblast heterogeneity in fibroblast-associated diseases.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2023
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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

6 authors at 1 institution in 1 country.

Yirong Chen *Department of Gastroenterology, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, No. 274 Zhijiang Road, Shanghai, 200071, China.
Renye Que *Department of Gastroenterology, Shanghai TCM Integrated Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200082, China.
Na ZhangDepartment of Gastroenterology, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, No. 274 Zhijiang Road, Shanghai, 200071, China.
Liubing LinDepartment of Gastroenterology, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, No. 274 Zhijiang Road, Shanghai, 200071, China.
Mengen ZhouDepartment of Gastroenterology, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, No. 274 Zhijiang Road, Shanghai, 200071, China.
Yong LiDepartment of Gastroenterology, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, No. 274 Zhijiang Road, Shanghai, 200071, China. liyong_sci@126.com.ORCID http://orcid.org/0000-0001-7971-4871
Shanghai University of Traditional Chinese Medicine · CN

Funding

national natural science foundation of china 81873157national natural science foundation of china No.81573775shanghai sailing program No. 19YF1445200the budgetary foundation of shanghai university of traditional chinese medicine No. 18LK074the budgetary foundation of shanghai university of traditional chinese medicine No. 2019LK032the youth talent training plan of shanghai municipal hospital of traditional chinese medicine No. 2019PY003
6 · The paper itself

Abstract

backgroundHepatic fibrosis is the final pathway of chronic liver disease characterized by excessive accumulation of extracellular matrix (ECM), which eventually develop into cirrhosis and liver cancer. Emerging studies demonstrated that Saikosaponin-d (SSd) exhibits a protective role in liver fibrosis. However, the mechanism underlying anti-liver fibrosis of SSd in vivo and in vitro remains unclear. METHODS AND

resultsTransforming growth factor (TGF)-β and carbon tetrachloride (CCl

conclusionsOur findings highlight that SSd alleviates hepatic fibrosis by regulating GPER1/autophagy pathway.

Indexed as

AnimalsAutophagyCarbon TetrachlorideCells, CulturedChinaFibrosisHepatic Stellate CellsHumansLiverLiver CirrhosisMaleMiceMice, Inbred C57BLOleanolic AcidReceptors, EstrogenReceptors, G-Protein-CoupledCarbon TetrachlorideGPER1 protein, mouseOleanolic AcidReceptors, EstrogenReceptors, G-Protein-Coupledsaikosaponin DSaponinsTransforming Growth Factor betaAutophagyG15GPER1Liver fibrosisSaikosaponin-d

Identifiers

PMID34714484
PMCPMC8604865
OpenAlexW3208900433

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.