Eukaryotic translation initiation factors and cancer

被引:43
作者
Ali, Muhammad Umar [1 ]
Rahman, Muhammad Saif Ur [1 ]
Jia, Zhenyu [2 ]
Jiang, Cao [1 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 2, Clin Res Ctr, Sch Med, 88 Jiefang Rd, Hangzhou 310009, Zhejiang, Peoples R China
[2] Zhejiang Acad Med Sci, Inst Occupat Dis, 182 Tianmushan Rd, Hangzhou 310013, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Translation; eukaryotic initiation factors; cancer; tumorigenesis; therapy; FACTOR 4E EIF4E; SQUAMOUS-CELL CARCINOMA; GUANINE-NUCLEOTIDE EXCHANGE; SIGNALING PATHWAY CONTRIBUTES; MESSENGER-RNA RECRUITMENT; 40-S RIBOSOMAL-SUBUNITS; BREAST-CANCER; MAMMALIAN TARGET; BINDING-PROTEIN; DECREASED EXPRESSION;
D O I
10.1177/1010428317709805
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent technological advancements have shown tremendous mechanistic accomplishments in our understanding of the mechanism of messenger RNA translation in eukaryotic cells. Eukaryotic messenger RNA translation is very complex process that includes four phases (initiation, elongation, termination, and ribosome recycling) and diverse mechanisms involving protein and non-protein molecules. Translation regulation is principally achieved during initiation step of translation, which is organized by multiple eukaryotic translation initiation factors. Eukaryotic translation initiation factor proteins help in stabilizing the formation of the functional ribosome around the start codon and provide regulatory mechanisms in translation initiation. Dysregulated messenger RNA translation is a common feature of tumorigenesis. Various oncogenic and tumor suppressive genes affect/are affected by the translation machinery, making the components of the translation apparatus promising therapeutic targets for the novel anticancer drug. This review provides details on the role of eukaryotic translation initiation factors in messenger RNA translation initiation, their contribution to onset and progression of tumor, and how dysregulated eukaryotic translation initiation factors can be used as a target to treat carcinogenesis.
引用
收藏
页码:1 / 19
页数:19
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