Recent advances in understanding the roles of matrix metalloproteinases in tumour invasion and metastasis

Guy A. Conlon, Graeme I. Murray* (Corresponding Author)

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

125 Citations (Scopus)
8 Downloads (Pure)

Abstract

This review aims to provide an overview of recent developments regarding the roles of matrix metalloproteinases in tumour invasion and metastasis. Much of the mortality burden belonging to cancer relates to its ability to invade adjacent tissue and form metastases at distant sites. This would not be possible without remodelling the extracellular matrix, a process which is enabled by the functions of matrix metalloproteinases. Recent studies provide a better understanding of the importance of the biophysical nature of the extracellular matrix, how this influences cancer cell motility, and how MMPs act to modify matrix stiffness. The regulation of matrix metalloproteinases and the role of immune cell generated matrix metalloproteinases has also become better understood. All of this provides a framework for the therapeutic targeting of matrix metalloproteinases and recent advances in the development of selective matrix metalloproteinases inhibitors are also reviewed.
Original languageEnglish
Pages (from-to)629-640
Number of pages12
JournalThe Journal of pathology
Volume247
Issue number5
Early online date15 Feb 2019
DOIs
Publication statusPublished - Apr 2019

Keywords

  • extracellular matrix
  • matrix metalloproteinase
  • metastasis
  • microenvironment
  • protease
  • tumour invasion
  • tumour progression
  • MMPs
  • ECM
  • TGF-BETA
  • DOWN-REGULATION
  • EPITHELIAL-MESENCHYMAL TRANSITION
  • LUNG METASTASIS
  • CELL-MIGRATION
  • COLORECTAL-CANCER
  • EXTRACELLULAR-MATRIX
  • TNF-ALPHA
  • TRANSFORMING-GROWTH-FACTOR
  • STROMAL CELLS

Fingerprint

Dive into the research topics of 'Recent advances in understanding the roles of matrix metalloproteinases in tumour invasion and metastasis'. Together they form a unique fingerprint.

Cite this