MMP1 drives tumor progression in large cell carcinoma of the lung through fibroblast senescence

Cancer Lett. 2021 Jun 1:507:1-12. doi: 10.1016/j.canlet.2021.01.028. Epub 2021 Mar 6.

Abstract

Large cell carcinoma (LCC) is a rare and aggressive lung cancer subtype with poor prognosis and no targeted therapies. Tumor-associated fibroblasts (TAFs) derived from LCC tumors exhibit premature senescence, and coculture of pulmonary fibroblasts with LCC cell lines selectively induces fibroblast senescence, which in turn drives LCC cell growth and invasion. Here we identify MMP1 as overexpressed specifically in LCC cell lines, and we show that expression of MMP1 by LCC cells is necessary for induction of fibroblast senescence and consequent tumor promotion in both cell culture and mouse models. We also show that MMP1, in combination with TGF-β1, is sufficient to induce fibroblast senescence and consequent LCC promotion. Furthermore, we implicate PAR-1 and oxidative stress in MMP1/TGF-β1-induced TAF senescence. Our results establish an entirely new role for MMP1 in cancer, and support a novel therapeutic strategy in LCC based on targeting senescent TAFs.

Keywords: Cancer-associated fibroblasts; MMP1; TGF-β; lung cancer; senescence.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cancer-Associated Fibroblasts / enzymology*
  • Cancer-Associated Fibroblasts / pathology
  • Carcinoma, Large Cell / enzymology*
  • Carcinoma, Large Cell / genetics
  • Carcinoma, Large Cell / pathology
  • Cell Line, Tumor
  • Cell Proliferation*
  • Cellular Senescence*
  • Coculture Techniques
  • Disease Progression
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Lung Neoplasms / enzymology*
  • Lung Neoplasms / genetics
  • Lung Neoplasms / pathology
  • Matrix Metalloproteinase 1 / genetics
  • Matrix Metalloproteinase 1 / metabolism*
  • Mice
  • Mice, Nude
  • Oxidative Stress
  • Paracrine Communication
  • Receptor, PAR-1 / genetics
  • Receptor, PAR-1 / metabolism
  • Signal Transduction
  • Transforming Growth Factor beta1 / genetics
  • Transforming Growth Factor beta1 / metabolism
  • Tumor Burden

Substances

  • Receptor, PAR-1
  • TGFB1 protein, human
  • Transforming Growth Factor beta1
  • MMP1 protein, human
  • Matrix Metalloproteinase 1