Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8644565 | Gene | 2018 | 4 Pages |
Abstract
Abnormal regulation of gene expression is essential for tumorigenesis. Several studies indicate that regulation of oncogene expression and neoplastic transformation are controlled by subunits of eukaryotic translation initiation factors (eIFs). Eukaryotic translation initiation factor 3 (eIF3) is the largest (800â¯kDa) and the most complex mammalian initiation factor. It is composed of 13 non-identical polypeptides designated as eIF3a-m and plays a pivotal role in protein synthesis that bridges the 43S pre-initiation complex and eIF4F-bound mRNA. However, the functional roles of individual subunits are not yet very clear. This review presents on several of aberrant expressed eIF3 subunits which are detected in various human cancers and the associated mechanisms have been acknowledged or are still not sure. Finally, identifying novel targets and biomarkers for caner is of great importance in early diagnosis and treatment of cancer. eIF3 may be a novel target molecule in drug development for cancer treatment and prevention.
Keywords
eIFsEukaryotic translation initiation factorseukaryotic translation initiation factor 3heterogeneous nuclear ribonucleoprotein UhnRNP Ucell division cycle 25APABPeIF3RRMCKIsCdc25aIRESccRCCMMTVNPCPARPNERSmall interfering RNARNA recognition motifsiRNAloss of heterozygositynucleotide excision repairTumorigenesisinternal ribosome entry siteCancerColorectal cancerNSCLCNon-small cell lung cancerGastric carcinomaClear cell renal cell carcinomawinged-helixLOHCyclin-dependent kinase inhibitorsHAMMouse mammary tumor viruspoly ADP-ribose polymeraseNasopharyngeal carcinomaCRC
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Authors
Yuting Yin, Jiali Long, Yanqin Sun, Hongmei Li, Enping Jiang, Chao Zeng, Wei Zhu,