Next-generation proteasome inhibitors for cancer therapy

Transl Res. 2018 Aug:198:1-16. doi: 10.1016/j.trsl.2018.03.002. Epub 2018 Mar 26.

Abstract

Over 2 decades ago, the proteasome was considered a risky or even untenable therapeutic target. Today, proteasome inhibitors are a mainstay in the treatment of multiple myeloma (MM) and have sales in excess of 3 billion US dollars annually. More importantly, the availability of proteasome inhibitors has greatly improved the survival and quality of life for patients with MM. Despite the remarkable success of proteasome inhibitor therapies to date, the potential for improvement remains, and the development and optimal use of proteasome inhibitors as anticancer agents continues to be an active area of research. In this review, we briefly discuss the features and limitations of the 3 proteasome inhibitor drugs currently used in the clinic and provide an update on current efforts to develop next-generation proteasome inhibitors with the potential to overcome the limitations of existing proteasome inhibitor drugs.

Publication types

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

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Boron Compounds / therapeutic use*
  • Bortezomib / therapeutic use*
  • Drug Resistance, Neoplasm
  • Glycine / analogs & derivatives*
  • Glycine / therapeutic use
  • Humans
  • Neoplasms / drug therapy*
  • Oligopeptides / therapeutic use*
  • Proteasome Inhibitors / therapeutic use*

Substances

  • Antineoplastic Agents
  • Boron Compounds
  • Oligopeptides
  • Proteasome Inhibitors
  • Bortezomib
  • ixazomib
  • carfilzomib
  • Glycine