Evidence map›Paper›PMID 41315577›Full record

ArticleScientific reports2025

Proteomic analysis of 7-octenoic acid antifibrotic effects in TGF-β1 activated hepatic stellate cells.

Watunyoo Buakaew, Kittipong Srimueang, Pornsuda Sutana, Yordhathai Thongsri, Pachuen Potup, Krai Daowtak, Sucheewin Krobthong, Yodying Yingchutrakul, Antonio Ferrante, Kanchana Usuwanthim

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Watunyoo BuakaewDepartment of Microbiology, Faculty of Medicine, Srinakharinwirot University, Bangkok, 10110, Thailand.
Kittipong SrimueangCellular and Molecular Immunology Research Unit (CMIRU), Faculty of Allied Health Sciences, Naresuan University, Phitsanulok, 65000, Thailand.
Pornsuda SutanaCellular and Molecular Immunology Research Unit (CMIRU), Faculty of Allied Health Sciences, Naresuan University, Phitsanulok, 65000, Thailand.
Yordhathai ThongsriCellular and Molecular Immunology Research Unit (CMIRU), Faculty of Allied Health Sciences, Naresuan University, Phitsanulok, 65000, Thailand.
Pachuen PotupCellular and Molecular Immunology Research Unit (CMIRU), Faculty of Allied Health Sciences, Naresuan University, Phitsanulok, 65000, Thailand.
Krai DaowtakCellular and Molecular Immunology Research Unit (CMIRU), Faculty of Allied Health Sciences, Naresuan University, Phitsanulok, 65000, Thailand.
Sucheewin KrobthongDepartment of Chemistry, Faculty of Science, Center of Excellence in Natural Products Chemistry (CENP), Chulalongkorn University, Bangkok, 10330, Thailand.
Yodying YingchutrakulNational Center for Genetic Engineering and Biotechnology, NSTDA, Pathum Thani, 12120, Thailand.
Antonio FerranteDepartment of Immunopathology, South Australia (SA) Pathology, Women's and Children's Hospital, North Adelaide, SA, Australia.
Kanchana UsuwanthimCellular and Molecular Immunology Research Unit (CMIRU), Faculty of Allied Health Sciences, Naresuan University, Phitsanulok, 65000, Thailand. kanchanau@nu.ac.th.

Funding

Global and Frontier Research University R2568C002Thailand Science Research and Innovation and Naresuan University R2569B106
6 · The paper itself

Abstract

Liver fibrosis represents the liver’s adaptive response to sustained and intense inflammation triggered by diverse insults, ranging from dietary factors to infectious agents. Although early-stage fibrosis can be reversible, unchecked progression often leads to cirrhosis and hepatocellular carcinoma. Therapeutic options remain limited, highlighting the pressing need for novel anti‑fibrotic agents. In this study, we evaluated the in vitro anti‑fibrotic effects of 7‑octenoic acid (7‑OCT), a bioactive constituent from Moringa oleifera Lam. Human hepatic stellate LX‑2 cells were stimulated with TGF‑β1 (10 ng/mL) in the presence or absence of 7‑OCT. Fibrotic marker expression was quantified at both the mRNA and protein levels. Comprehensive proteomic profiling and subsequent in silico docking analyses were performed to identify putative molecular targets and clarify mechanisms of action. Our results demonstrate that 7‑OCT significantly suppresses the expression of α‑smooth muscle actin (α‑SMA), collagen type I, and matrix metalloproteinase‑9 (MMP‑9) by downregulating transforming growth factor beta receptor 1 (TGFBR1) expression and inhibiting mothers against decapentaplegic homolog 3 (SMAD3) phosphorylation. Proteomic data implicates focal adhesion pathway proteins in mediating these effects. Collectively, these findings suggest that 7‑OCT is a promising lead compound for the development of anti‑fibrotic therapies.

Indexed as

Antifibrotic AgentsHepatic Stellate CellsLiver CirrhosisProteomeProteomicsTransforming Growth Factor beta1Cell LineHumansSmad3 ProteinAntifibrotic AgentsProteomeSmad3 ProteinTransforming Growth Factor beta17-octenoic acidHepatic stellate cellLiver fibrosisMoringa Oleifera lam.Proteomics

Identifiers

PMID41315577
PMCPMC12753640

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.