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Proteomic analysis of 7-octenoic acid antifibrotic effects in TGF-β1 activated hepatic stellate cells
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Metadata
Document Title
Proteomic analysis of 7-octenoic acid antifibrotic effects in TGF-β1 activated hepatic stellate cells
Author
Buakaew W.
Name from Authors Collection
Affiliations
Department of Microbiology, Faculty of Medicine, Srinakharinwirot University, Bangkok, 10110, Thailand; Cellular and Molecular Immunology Research Unit (CMIRU), Faculty of Allied Health Sciences, Naresuan University, Phitsanulok, 65000, Thailand; Department of Chemistry, Faculty of Science, Center of Excellence in Natural Products Chemistry (CENP), Chulalongkorn University, Bangkok, 10330, Thailand; National Center for Genetic Engineering and Biotechnology, NSTDA, Pathum Thani, 12120, Thailand; Department of Immunopathology, South Australia (SA) Pathology, Women’s and Children’s Hospital, North Adelaide, SA, Australia; Department of Paediatrics, Adelaide School of Medicine, University of Adelaide, Adelaide, 5000, SA, Australia; Department of Molecular and Biomedical Science, School of Biological Science and the Robinson Research Institute, University of Adelaide, Adelaide, 5000, SA, Australia
Type
Article
Source Title
Scientific Reports
ISSN
20452322
Year
2025
Volume
15
Issue
1
Open Access
All Open Access; Gold Open Access; Green Open Access
Publisher
Nature Research
DOI
10.1038/s41598-025-29722-8
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. © The Author(s) 2025.
License
CC BY-NC-ND
Rights
Authors
Publication Source
Scopus