Future Therapeutic Directions for Smac-Mimetics

Cells. 2020 Feb 11;9(2):406. doi: 10.3390/cells9020406.

Abstract

It is well accepted that the ability of cancer cells to circumvent the cell death program that untransformed cells are subject to helps promote tumor growth. Strategies designed to reinstate the cell death program in cancer cells have therefore been investigated for decades. Overexpression of members of the Inhibitor of APoptosis (IAP) protein family is one possible mechanism hindering the death of cancer cells. To promote cell death, drugs that mimic natural IAP antagonists, such as second mitochondria-derived activator of caspases (Smac/DIABLO) were developed. Smac-Mimetics (SMs) have entered clinical trials for hematological and solid cancers, unfortunately with variable and limited results so far. This review explores the use of SMs for the treatment of cancer, their potential to synergize with up-coming treatments and, finally, discusses the challenges and optimism facing this strategy.

Keywords: IAPs; Smac-Mimetics; Smac/DIABLO; TNF; cancer; cell death.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antineoplastic Agents / therapeutic use
  • Apoptosis / drug effects
  • Apoptosis Regulatory Proteins / genetics*
  • Apoptosis Regulatory Proteins / therapeutic use
  • Baculoviral IAP Repeat-Containing 3 Protein / genetics*
  • Biomimetics
  • Cell Proliferation / drug effects
  • Clinical Trials as Topic
  • Humans
  • Inhibitor of Apoptosis Proteins / genetics*
  • Mitochondrial Proteins / genetics*
  • Mitochondrial Proteins / therapeutic use
  • Neoplasms / drug therapy*
  • Neoplasms / genetics
  • Neoplasms / pathology
  • Protein Binding

Substances

  • Antineoplastic Agents
  • Apoptosis Regulatory Proteins
  • DIABLO protein, human
  • Inhibitor of Apoptosis Proteins
  • Mitochondrial Proteins
  • BIRC3 protein, human
  • Baculoviral IAP Repeat-Containing 3 Protein