Targeting Legumain As a Novel Therapeutic Strategy in Cancers

Curr Drug Targets. 2017;18(11):1259-1268. doi: 10.2174/1389450117666161216125344.

Abstract

Background: Recent reports indicate that the tumor microenvironment plays a pivotal role in cancer development and progression, leading to a paradigm shift in the way cancer is studied and targeted. In contrast to traditional approaches, where only tumor cells are targeted for the treatment, an emerging approach is to develop therapeutics which target the tumor microenvironment while complementing or enhancing current treatments. Legumain (LGMN) is a newly identified target which is highly expressed in the tumor microenvironment and in tumor cells, and holds potential both as a biomarker and as a therapeutic target.

Conclusion: This review will be the first to summarize the expression of LGMN in common cancers, as well as its roles in tumorigenesis and metastasis. This review also discusses the current developments and future prospects of targeting LGMN through the development of DNA vaccines, azopeptides, small molecule inhibitors and LGMN activated prodrugs, highlighting the potential of LGMN as a target for cancer therapeutics.

Keywords: Legumain; azo-peptide; cancer; prodrug; small molecules; tumor microenvironment; vaccine.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / therapeutic use
  • Cysteine Endopeptidases / metabolism*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Molecular Targeted Therapy
  • Neoplasm Metastasis
  • Neoplasms / drug therapy*
  • Neoplasms / metabolism
  • Small Molecule Libraries / pharmacology
  • Small Molecule Libraries / therapeutic use
  • Tumor Microenvironment
  • Up-Regulation
  • Vaccines, DNA / pharmacology
  • Vaccines, DNA / therapeutic use

Substances

  • Antineoplastic Agents
  • Small Molecule Libraries
  • Vaccines, DNA
  • Cysteine Endopeptidases
  • asparaginylendopeptidase