| Literature DB >> 28965870 |
Marise R Heerma van Voss1, Paul J van Diest2, Venu Raman3.
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.Entities:
Keywords: DDX; DDX3; RNA helicase; Translation; eIF4A
Mesh:
Substances:
Year: 2017 PMID: 28965870 PMCID: PMC5675762 DOI: 10.1016/j.bbcan.2017.09.006
Source DB: PubMed Journal: Biochim Biophys Acta Rev Cancer ISSN: 0304-419X Impact factor: 10.680