The paradoxical role of matrix metalloproteinase-11 in cancer

Biomed Pharmacother. 2021 Sep:141:111899. doi: 10.1016/j.biopha.2021.111899. Epub 2021 Jul 30.

Abstract

The microenvironment surrounding the tumor affects biological processes, such as cell proliferation, angiogenesis, apoptosis, and invasion. Therefore, the ability to change these environments is an important attribute for tumor cells to obtain specific functions necessary for growth and metastasis. Matrix metalloproteinases (MMPs) are zinc-dependent proteolytic metalloenzymes that facilitate protease-dependent tumor progression by degrading extracellular matrix (ECM) proteins, releasing cytokines, growth factors, and other cell surface molecules. As one of the most widely studied MMPs, MMP-11 is an important protease that is expressed in cancer cells, stromal cells, and the adjacent microenvironment. MMP-11 has a dual effect on tumors. On one hand, MMP-11 promotes tumor development by inhibiting apoptosis and promoting the migration and invasion of cancer cells in the early stage. On the other hand, in animal models, MMP-11 has a protective effect on tumor growth and metastasis at an advanced stage. Based on current findings regarding the importance of MMP-11 in altering the tumor microenvironment, there is a need to further understand how stromal cells and the ECM regulate tumor progression, which may result in the re-examination of MMPs as drug targets for cancer and other diseases. In this review, we summarize the dual role of MMP-11 in cancer and its potential clinical significance.

Keywords: Biomarker; Cancer; Diagnosis; Matrix metalloproteinase-11 (MMP-11); Microenvironment.

Publication types

  • Review

MeSH terms

  • Animals
  • Biomarkers
  • Humans
  • Matrix Metalloproteinase 11 / metabolism
  • Matrix Metalloproteinase 11 / physiology*
  • Neoplasms / enzymology*
  • Neoplasms / physiopathology*
  • Neovascularization, Pathologic
  • Stromal Cells / enzymology
  • Tumor Microenvironment

Substances

  • Biomarkers
  • Matrix Metalloproteinase 11