論文

2005年9月

Extracellular matrix remodeling in oral submucous fibrosis: its stage-specific modes revealed by immunohistochemistry and in situ hybridization

JOURNAL OF ORAL PATHOLOGY & MEDICINE
  • H Utsunomiya
  • ,
  • WM Tilakaratne
  • ,
  • K Oshiro
  • ,
  • S Maruyama
  • ,
  • M Suzuki
  • ,
  • H Ida-Yonemochi
  • ,
  • J Cheng
  • ,
  • T Saku

34
8
開始ページ
498
終了ページ
507
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1111/j.1600-0714.2005.00339.x
出版者・発行元
BLACKWELL PUBLISHING

BACKGROUND: Oral submucous fibrosis (OSF) is a chewing habit-related pre-cancerous condition of the oral mucosa affecting predominantly south Asians. It is histopathologically characterized by epithelial atrophy and fibrosis of the subepithelial connective tissue. Fibrosis extends all the way into the muscle layer, leading to difficulty in mouth opening. However, the dynamics of extracellular matrix (ECM) remodeling with OSF progression is largely unknown.
METHODS: Forty biopsy specimens of OSF and 10 of normal buccal mucosa were examined for expression/deposition modes of eight ECM molecules by histochemistry, immunohistochemistry, and in situ hybridization.
RESULTS: In the early stage of OSF, tenascin, perlecan, fibronectin, collagen type III were characteristically enhanced in the lamina propria and the submucosal layer. In the intermediate stage, the ECM molecules mentioned above and elastin were extensively and irregularly deposited around muscle fibers. In the advanced stage, such ECM depositions decreased and were entirely replaced with collagen type I only. Their gene expression levels varied with progression of fibrosis, but the mRNA signals were confirmed in fibroblasts in the submucosal fibrotic areas.
CONCLUSIONS: The results indicate that the ECM remodeling steps in OSF are similar to each phase of usual granulation tissue formation. Restricted mouth opening may be a result of loss of variety of ECM molecules including elastin into the homogeneity of collagen type I replacing muscle fibers.

リンク情報
DOI
https://doi.org/10.1111/j.1600-0714.2005.00339.x
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000230888600008&DestApp=WOS_CPL
ID情報
  • DOI : 10.1111/j.1600-0714.2005.00339.x
  • ISSN : 0904-2512
  • Web of Science ID : WOS:000230888600008

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