Kallikrein-related peptidase 7 overexpression in melanoma cells modulates cell adhesion leading to a malignant phenotype

Biol Chem. 2018 Sep 25;399(9):1099-1105. doi: 10.1515/hsz-2017-0339.

Abstract

We recently reported that human melanoma cells, but not benign melanocytes, aberrantly express kallikrein-related peptidase 7 (KLK7). Here, we show a KLK7 overexpression-mediated decrease of cell adhesion to extracellular matrix binding proteins, associated with downregulation of α5/β1/αv/β3 integrin expression. We also report an up-regulation of MCAM/CD146 and an increase in spheroid formation of these cells. Our results demonstrate that aberrant KLK7 expression leads to a switch to a more malignant phenotype suggesting a potential role of KLK7 in melanoma invasion. Thus, KLK7 may represent a biomarker for melanoma progression and may be a potential therapeutic target for melanoma.

Keywords: E-cadherin; MCAM/CD146; integrins; kallikrein-related peptidase 7; melanoma; spheroid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism
  • Cell Adhesion / genetics
  • Down-Regulation
  • Humans
  • Integrins / biosynthesis
  • Kallikreins / genetics*
  • Kallikreins / metabolism*
  • Melanoma / genetics*
  • Melanoma / metabolism
  • Melanoma / pathology*
  • Phenotype

Substances

  • Biomarkers, Tumor
  • Integrins
  • KLK7 protein, human
  • Kallikreins