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Abstract
The matrix metalloproteinases (MMPs) can degrade a range of extracellular matrix proteins
and have been implicated in connective tissue destruction and remodelling associated
with cancer invasion and metastasis, cartilage destruction in arthritis, atherosclerotic
plaque rupture, and the development of aneurysms. Recently, naturally occurring sequence
variation has been detected in the promoter of a number of MMP genes. These genetic
polymorphisms have been shown to have allele-specific effects on the transcriptional
activities of MMP gene promoters, and to be associated with susceptibility to coronary
heart disease, aneurysms and cancers. These findings indicate that variation in the
MMP genes may contribute to inter-individual differences in susceptibility to these
common, complex diseases, likely through effects on the balance between the synthesis
and degradation of extracellular matrix proteins.