Targeting RNA helicases in cancer: The translation trap

Biochim Biophys Acta Rev Cancer. 2017 Dec;1868(2):510-520. doi: 10.1016/j.bbcan.2017.09.006. Epub 2017 Sep 28.

Abstract

Cancer cells are reliant on the cellular translational machinery for both global elevation of protein synthesis and the translation of specific mRNAs that promote tumor cell survival. Targeting translational control in cancer is therefore increasingly recognized as a promising therapeutic strategy. In this regard, DEAD/H box RNA helicases are a very interesting group of proteins, with several family members regulating mRNA translation in cancer cells. In this review, we delineate the mechanisms by which DEAD/H box proteins modulate oncogenic translation and how inhibition of these RNA helicases can be exploited for anti-cancer therapeutics.

Keywords: DDX; DDX3; RNA helicase; Translation; eIF4A.

Publication types

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

MeSH terms

  • 5' Untranslated Regions
  • Carcinogenesis
  • DEAD-box RNA Helicases / antagonists & inhibitors
  • DEAD-box RNA Helicases / physiology
  • Eukaryotic Initiation Factor-4A / antagonists & inhibitors
  • Eukaryotic Initiation Factor-4A / physiology
  • Humans
  • Neoplasms / drug therapy*
  • Neoplasms / metabolism
  • Protein Biosynthesis / drug effects*
  • RNA Helicases / antagonists & inhibitors*
  • RNA Helicases / physiology

Substances

  • 5' Untranslated Regions
  • Eukaryotic Initiation Factor-4A
  • DDX3X protein, human
  • DEAD-box RNA Helicases
  • RNA Helicases