Evidence map›Paper›PMID 36406310›Full record

ArticleJournal of clinical and translational hepatology2023

Upregulation of GLT25D1 in Hepatic Stellate Cells Promotes Liver Fibrosis via the TGF-β1/SMAD3 Pathway

Shiwei Wang, Lingling He, Fan Xiao, Meixin Gao, Herui Wei, Junru Yang, Yang Shu, Fuyang Zhang, Xiaohui Ye, Ping Li and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of clinical and translational hepatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 8 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Shiwei WangDepartment of Gastroenterology, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Lingling HeDepartment of Gastroenterology, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Fan XiaoInstitute of Infectious Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Meixin GaoDepartment of Gastroenterology, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Herui WeiDepartment of Gastroenterology, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Junru YangDepartment of Gastroenterology, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Yang ShuDepartment of Gastroenterology, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Fuyang ZhangDepartment of Gastroenterology, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Xiaohui YeDepartment of Gastroenterology, Beijing Huaxin Hospital, the First Affiliated Hospital of Tsinghua University, Beijing, China.
Ping LiDepartment of Gastroenterology, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Xiaohua HaoBeijing Ditan Hospital, Capital Medical University, Beijing, China.
Xingang ZhouDepartment of Pathology, Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Hongshan WeiDepartment of Gastroenterology, Beijing Ditan Hospital, Capital Medical University, Beijing, China.ORCID https://orcid.org/0000-0001-8893-653X
Capital Medical University · CNBeijing Hua Xin Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Collagen β(1-O) galactosyltransferase 25 domain 1 (GLT25D1) is associated with collagen production and glycosylation, and its knockout in mice results in embryonic death. However, its role in liver fibrosis remains elusive, particularly in hepatic stellate cells (HSCs), the primary collagen-producing cells associated with liver fibrogenesis. Herein, we aimed to elucidate the role of GLT25D1 in HSCs. Methods: Bile duct ligation (BDL)-induced mouse liver fibrosis models, primary mouse HSCs (mHSCs), and transforming growth factor beta 1 (TGF-β1)-stimulated LX-2 human hepatic stellate cells were used in Results: GLT25D1 expression was upregulated in nonparenchymal cells in human cirrhotic liver tissues. Meanwhile, its knockdown attenuated collagen deposition in BDL-induced mouse liver fibrosis and inhibited mHSC activation. GLT25D1 was overexpressed in activated versus quiescence LX-2 cells and regulated Conclusions: Collectively, the upregulation of GLT25D1 in HSCs promoted the progression of liver fibrosis by affecting HSCs activation and collagen stability.

Indexed as

CollagenGlycosylationHepatic stellate cellsLiver fibrosisTGF-β1

Identifiers

PMID36406310
PMCPMC9647113
OpenAlexW4281552134

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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.