Lumican and decorin are differentially expressed in human breast carcinoma

J Pathol. 2000 Nov;192(3):313-20. doi: 10.1002/1096-9896(200011)192:3<313::AID-PATH694>3.0.CO;2-B.

Abstract

Previous studies have shown that lumican is expressed and increased in the stroma of breast tumours. Lumican expression has now been examined relative to other members of the small leucine-rich proteoglycan gene family in normal and neoplastic breast tissues, to begin to determine its role in breast tumour progression. Western blot study showed that lumican protein is highly abundant relative to decorin, while biglycan and fibromodulin are only detected occasionally in breast tissues (n=15 cases). Further analysis of lumican and decorin expression performed in matched normal and tumour tissues by in situ hybridization showed that both mRNAs were expressed by similar fibroblast-like cells adjacent to epithelium. However, lumican mRNA expression was significantly increased in tumours (n=34, p<0.0001), while decorin mRNA was decreased (p=0.0002) in neoplastic relative to adjacent normal stroma. This was accompanied by a significant increase in lumican protein (n=12, p=0.0122), but not decorin. Further evidence of altered lumican expression in breast cancer was manifested by discordance between lumican mRNA and protein localization in some regions of tumours but not in adjacent morphologically normal tissues. It is concluded that lumican is the most abundant of these proteoglycans in breast tumours and that lumican and decorin are inversely regulated in association with breast tumourigenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Biomarkers, Tumor
  • Blotting, Western
  • Breast Neoplasms / metabolism*
  • Case-Control Studies
  • Disease Progression
  • Electrophoresis, Polyacrylamide Gel
  • Female
  • Gene Expression
  • Humans
  • In Situ Hybridization
  • Middle Aged
  • Proteoglycans / genetics
  • Proteoglycans / metabolism*
  • RNA, Messenger / analysis

Substances

  • Biomarkers, Tumor
  • Proteoglycans
  • RNA, Messenger