MT1-MMP and MMP-7 in invasion and metastasis of human cancers

Cancer Metastasis Rev. Jun-Sep 2003;22(2-3):145-52. doi: 10.1023/a:1023039230052.

Abstract

Previous experimental and biochemical studies on matrix metalloproteinases (MMPs) have indicated that MMPs are implicated in cancer invasion and metastases. Studies on the expression of MMPs and tissue inhibitors of metalloproteinases (TIMPs) in various human cancer tissues have further demonstrated that activation of proMMP-2 mediated by a combination of TIMP-2 and MT1-MMP (the proMMP-2/TIMP-2/MT1-MMP system) correlates well with the progression of most of these cancers such as the breast carcinomas, thyroid papillary carcinomas, gastric adenocarcinomas, oral squamous cell carcinomas and gliomas, whereas MMP-7 plays an important role in the metastases of endometrial and gastrointestinal carcinomas. Although MMP-7 is a typical secreted MMP, a member of transmembrane 4 superfamily (TM4SF) captures proMMP-7 on the carcinoma cell membranes through interaction with its propeptide, leading to its pericellular activation. Thus, these results strongly suggest that proteolysis at the cell-extracellular matrix interfaces of cancer cells by the proMMP-2/TIMP-2/MT1-MMP and proMMP-7/TM4SF systems plays crucial roles in the progression of human cancers. In this article, we address the current views on the roles of these MMPs acting onthe cell membranes in human cancer invasion and metastases.

Publication types

  • Review

MeSH terms

  • Animals
  • Extracellular Matrix / enzymology
  • Gene Expression Regulation, Enzymologic
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Matrix Metalloproteinase 7 / physiology*
  • Matrix Metalloproteinases, Membrane-Associated
  • Metalloendopeptidases / physiology*
  • Neoplasm Invasiveness*
  • Neoplasm Metastasis*
  • Neoplasms / enzymology*
  • Tissue Inhibitor of Metalloproteinase-2 / metabolism

Substances

  • Tissue Inhibitor of Metalloproteinase-2
  • Matrix Metalloproteinases, Membrane-Associated
  • Metalloendopeptidases
  • Matrix Metalloproteinase 7