Targeting cathepsin S induces tumor cell autophagy via the EGFR-ERK signaling pathway

Cancer Lett. 2012 Apr 1;317(1):89-98. doi: 10.1016/j.canlet.2011.11.015. Epub 2011 Nov 18.

Abstract

Cathepsin S is a cellular cysteine protease, which is frequently over-expressed in human cancer cells and plays important role in tumor metastasis. However, the role of cathepsin S in regulating cancer cell survival and death remains undefined. The aim of this study was to determine whether targeting cathepsin S could induce autophagy/apoptosis in cancer cells. In this study, we demonstrated that targeting cathepsin S by either specific small molecular inhibitors or cathepsin S siRNA induced autophagy and subsequent apoptosis in human cancer cells, and the induction of autophagy was dependent on the phosphorylation of EGFR and activation of the EGFR-related ERK/MAPK-signaling pathway. In conclusion, the current study reveals that cathepsin S plays an important role in the regulation of cell autophagy through interference with the EGFR-ERK/MAPK-signaling pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology*
  • Autophagy / drug effects*
  • CHO Cells
  • Cathepsins / antagonists & inhibitors*
  • Cathepsins / genetics
  • Cathepsins / metabolism
  • Cricetinae
  • Cricetulus
  • Dose-Response Relationship, Drug
  • Enzyme Activation
  • ErbB Receptors / metabolism*
  • Extracellular Signal-Regulated MAP Kinases / metabolism*
  • HT29 Cells
  • Humans
  • Molecular Targeted Therapy
  • Neoplasms / enzymology*
  • Neoplasms / genetics
  • Neoplasms / pathology
  • Phosphorylation
  • Protein Kinase Inhibitors / pharmacology*
  • RNA Interference
  • Signal Transduction / drug effects*
  • Time Factors
  • Transfection

Substances

  • Antineoplastic Agents
  • Protein Kinase Inhibitors
  • EGFR protein, human
  • ErbB Receptors
  • Extracellular Signal-Regulated MAP Kinases
  • Cathepsins
  • cathepsin S