Literature DB >> 19330028

Analysis of the matrix metalloproteinase family reveals that MMP8 is often mutated in melanoma.

Lavanya H Palavalli1, Todd D Prickett, John R Wunderlich, Xiaomu Wei, Allison S Burrell, Patricia Porter-Gill, Sean Davis, Chenwei Wang, Julia C Cronin, Neena S Agrawal, Jimmy C Lin, Wendy Westbroek, Shelley Hoogstraten-Miller, Alfredo A Molinolo, Patricia Fetsch, Armando C Filie, Michael P O'Connell, Carolyn E Banister, Jason D Howard, Phillip Buckhaults, Ashani T Weeraratna, Lawrence C Brody, Steven A Rosenberg, Yardena Samuels.   

Abstract

A mutational analysis of the matrix metalloproteinase (MMP) gene family in human melanoma identified somatic mutations in 23% of melanomas. Five mutations in one of the most commonly mutated genes, MMP8, reduced MMP enzyme activity. Expression of wild-type but not mutant MMP8 in human melanoma cells inhibited growth on soft agar in vitro and tumor formation in vivo, suggesting that wild-type MMP-8 has the ability to inhibit melanoma progression.

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Year:  2009        PMID: 19330028      PMCID: PMC2748394          DOI: 10.1038/ng.340

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


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10.  Upregulation of MMP-2 by HMGA1 promotes transformation in undifferentiated, large-cell lung cancer.

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