Inhibition of hyaluronan synthases decreases matrix metalloproteinase-7 (MMP-7) expression and activity

Kelli M. Bullard Dunn, Peter K. Lee, Christopher M. Wilson, Joji Iida, Karen R. Wasiluk, Marie Hugger, James B. McCarthy

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Introduction: Hyaluronan (HA) and its biosynthetic enzymes hyaluronan synthases (HAS2 and HAS3) mediate Matrigel invasion by SW620 colon carcinoma cells. Because matrix metalloproteinases (MMPs) have been implicated in cancer invasion, we hypothesized that changes in HAS expression would alter MMP expression and activity in these cells. Methods: To determine whether an MMP was involved in invasion, Matrigel invasion assays with SW620 cells were performed in the presence or absence of the MMP inhibitors GM6001 or TIMP2. HAS isozymes were inhibited by stably transfecting SW620 cells with vectors that contained antisense HAS2 and/or -3 cDNA; transfection with an empty vector served as a control. MMP-7 transcription was assessed by quantitative reverse transcription polymerase chain reaction (RT-PCR). MMP-7 protein was detected by enzyme-linked immunosorbent assay (ELISA) and enzymatic activity compared using zymography. Results: GM6001 and TIMP2 decreased Matrigel invasion, which confirms that an MMP played a key role in this process. MMP-7 expression was then detected in SW620 cells. Finally, MMP-7 expression, protein, and enzymatic activity were significantly lower in antisense HAS tranfectants than in SW620 or vector control cells. Conclusion: We have demonstrated previously that inhibition of HAS expression and HA production in SW620 colon carcinoma cells inhibits Matrigel invasion. In the studies presented here, we have demonstrated that SW620 cells express high levels of MMP-7 and that inhibition of HAS isozymes dramatically decreases MMP-7 expression, protein, and enzymatic activity. Taken together, these findings suggest that HAS and HA may mediate cellular invasion via changes in MMP-7 expression.

Original languageEnglish (US)
Pages (from-to)322-329
Number of pages8
JournalSurgery
Volume145
Issue number3
DOIs
StatePublished - Mar 2009

Bibliographical note

Funding Information:
Supported in part by the Society of University Surgeons Junior Faculty Award, the Wyeth-SUS Foundation Clinical Scholar Award, and the American Society of Colon and Rectal Surgeons Foundation Career Development Award.

Copyright:
Copyright 2009 Elsevier B.V., All rights reserved.

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