Expression cloning of novel regulators of 92 kDa type IV collagenase expression

R. R. Nair, D. D. Boyd

Research output: Contribution to journalShort surveypeer-review

13 Scopus citations

Abstract

Overexpression of the 92 kDa type IV collagenase (MMP-9) contributes to cancer progression. However, to date, there are few known regulators of expression of this metalloproteinase. We employed an expression library comprising 500 000 cDNA clones to screen for novel regulators of MMP-9 expression. HT1080 cells were transiently co-transfected with an MMP-9 promoter-luciferase reporter and pools of the cDNA expression library. Positive-scoring pools were subdivided in secondary and tertiary screens, after which the regulatory cDNAs were identified by DNA sequencing. This brief review illustrates the utility of expression cloning in identifying specific regulators of MMP-9 expression.

Original languageEnglish (US)
Pages (from-to)1135-1136
Number of pages2
JournalBiochemical Society Transactions
Volume33
Issue number5
DOIs
StatePublished - Nov 2005

Keywords

  • 92 kDa type IV collagenase
  • Cancer
  • Expression cloning strategy
  • HT1080 cells
  • Matrix metalloproteinase-9 (MMP-9)
  • Tumour progression

ASJC Scopus subject areas

  • Biochemistry

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