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Alpha v beta 6 integrin down-regulates the MMP-13 expression in oral squamous cell carcinoma cells.

Abstract
The integrin alphavbeta6, a receptor for fibronectin, vitronectin, tenascin and TGF-beta latency-associated peptide (LAP), is not detectable on normal oral epithelium but is neo-expressed in oral squamous cell carcinomas (OSCC) and epithelial dysplasia. Previously it has been shown that alphavbeta6 integrin can up-regulate MMP-3 and -9 expression in OSCC cells. Using beta6-transfected and control OSCC cells we demonstrate that alphavbeta6 integrin down-regulates MMP-13 expression at both mRNA and protein level. Although expressing less MMP-13, beta6-transfected cells were found to have similar collagenolytic activity as control cells and invade at similar levels through type I collagen. Growth of the tumour cells in organotypic culture and confocal microscopy confirmed low levels of MMP-13 in cells with high alphavbeta6 expression. Furthermore, human squamous cell carcinomas of the tongue with high expression of alphavbeta6 showed lower MMP-13 levels than carcinomas with low levels of alphavbeta6. Our results suggest that alphavbeta6 down-regulates MMP-13 expression in OSCC cells and that MMP-13 is not essential for the degradation of type I collagen by OSCC cells.
AuthorsM Ylipalosaari, G J Thomas, M Nystrom, S Salhimi, J F Marshall, V Huotari, T Tervahartiala, T Sorsa, T Salo
JournalExperimental cell research (Exp Cell Res) Vol. 309 Issue 2 Pg. 273-83 (Oct 01 2005) ISSN: 0014-4827 [Print] United States
PMID16024014 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antigens, Neoplasm
  • Collagen Type I
  • Integrins
  • Matrix Metalloproteinase Inhibitors
  • Membrane Proteins
  • RNA, Messenger
  • integrin alphavbeta6
  • Collagenases
  • MMP13 protein, human
  • Matrix Metalloproteinase 13
  • Matrix Metalloproteinase 8
  • Matrix Metalloproteinase 1
Topics
  • Antigens, Neoplasm (physiology)
  • Carcinoma, Squamous Cell (enzymology)
  • Cell Line, Tumor
  • Collagen Type I (antagonists & inhibitors, metabolism)
  • Collagenases (biosynthesis, genetics)
  • Down-Regulation (physiology)
  • Gene Expression Regulation, Neoplastic (physiology)
  • Humans
  • Integrins (physiology)
  • Matrix Metalloproteinase 1 (biosynthesis, genetics)
  • Matrix Metalloproteinase 13
  • Matrix Metalloproteinase 8 (biosynthesis, genetics)
  • Matrix Metalloproteinase Inhibitors
  • Membrane Proteins (antagonists & inhibitors, biosynthesis, genetics)
  • Mouth Neoplasms (enzymology, metabolism)
  • RNA, Messenger (antagonists & inhibitors, metabolism)

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