Proteases as activators for cytotoxic prodrugs in antitumor therapy

Cancer Genomics Proteomics. 2014 Mar-Apr;11(2):67-79.

Abstract

Proteases are often overexpressed in tumor cells and/or the stromal compartment and can thus be exploited in tumor therapy to activate cytotoxic prodrugs as, for example, in cytolytic fusion proteins, and for tumor imaging. Specifically, we discuss cathepsin B-activated prodrug conjugates, antibody-directed prodrug therapy, protease-activated peptide-thapsigargin conjugates, protease-activated cytotoxic receptor ligands and other cytotoxic proteins, protease-mediated activation of anthrax toxin, granzyme B as a therapeutic principle in cytolytic fusion proteins, and tumor-imaging based on deregulated proteases.

Keywords: Anthrax toxin; Antibody-drug conjugates; antibody-directed enzyme prodrug therapy; cytotoxic receptor ligand(s); granzyme B; probody; review; thapsigargin.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / metabolism*
  • Antineoplastic Agents / therapeutic use
  • Cathepsin B / physiology
  • Granzymes / physiology
  • Humans
  • Matrix Metalloproteinases / physiology
  • Neoplasms / drug therapy*
  • Prodrugs / metabolism*
  • Prodrugs / therapeutic use
  • Proteolysis
  • Serine Endopeptidases / physiology
  • Urokinase-Type Plasminogen Activator / physiology

Substances

  • Antineoplastic Agents
  • Prodrugs
  • GZMB protein, human
  • Granzymes
  • Serine Endopeptidases
  • ST14 protein, human
  • Urokinase-Type Plasminogen Activator
  • CTSB protein, human
  • Cathepsin B
  • Matrix Metalloproteinases