Abstract | BACKGROUND/PURPOSE:
Connective tissue growth factor (CCN2) has been associated with the pathogenesis of various fibrotic diseases, including oral submucous fibrosis (OSF). The chemical constituents of areca nut along with the mechanical trauma cause OSF. The coarse fibers of areca nut injure the mucosa and hence sphingosine-1-phosphate (S1P) is released at the wounded sites. Recent studies have shown that S1P is involved in wound healing and the development of fibrosis. The aims of this study were to investigate the effects of S1P on CCN2 expression in human buccal fibroblasts (HBFs) and identify the potential targets for drug intervention or chemoprevention of OSF. METHODS: Western blot analyses were used to study the effects of S1P on CCN2 expression and its signaling pathways in HBFs and whether epigallocatechin-3-gallate (EGCG), the main and most significant polyphenol in green tea, could inhibit this pathway. RESULTS: CONCLUSION: S1P released by repetitive mechanical trauma during AN chewing may contribute to the pathogenesis of OSF through upregulating CCN2 expression in HBFs. EGCG could be an adjuvant to the current offered therapy options or the prevention of OSF through suppression of JNK activation.
|
Authors | Jenny I-Chun Sar, Chih-Jen Yang, Yi-Shin Tsai, Yi-Ting Deng, Hsin-Ming Chen, Hao-Hueng Chang, Cheing-Meei Liu |
Journal | Journal of the Formosan Medical Association = Taiwan yi zhi
(J Formos Med Assoc)
Vol. 114
Issue 9
Pg. 860-4
(Sep 2015)
ISSN: 0929-6646 [Print] Singapore |
PMID | 24035571
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Copyright | Copyright © 2013. Published by Elsevier B.V. |
Chemical References |
- CCN2 protein, human
- Lysophospholipids
- Connective Tissue Growth Factor
- sphingosine 1-phosphate
- Catechin
- epigallocatechin gallate
- Extracellular Signal-Regulated MAP Kinases
- p38 Mitogen-Activated Protein Kinases
- Sphingosine
|
Topics |
- Areca
- Catechin
(analogs & derivatives, pharmacology)
- Cells, Cultured
- Connective Tissue Growth Factor
(metabolism)
- Extracellular Signal-Regulated MAP Kinases
(antagonists & inhibitors)
- Fibroblasts
(drug effects)
- Humans
- Lysophospholipids
(pharmacology)
- Oral Submucous Fibrosis
(physiopathology)
- Signal Transduction
(drug effects)
- Sphingosine
(analogs & derivatives, pharmacology)
- Up-Regulation
(drug effects)
- p38 Mitogen-Activated Protein Kinases
(antagonists & inhibitors)
|