The reciprocal link between EVI1 and miRNAs in human malignancies

被引:6
|
作者
Lang, Wen-Jing [1 ]
Chen, Fang-Yuan [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Renji Hosp, Dept Hematol, Shanghai 200127, Peoples R China
基金
中国国家自然科学基金;
关键词
Ecotropic virus integration site-1 (EVI1); Non-coding RNAs; MicroRNAs; Transcription factor; Reciprocal link; Human malignancies; ACUTE MYELOID-LEUKEMIA; NEGATIVE FEEDBACK LOOP; VIRAL INTEGRATION SITE; BREAST-CANCER CELLS; DOWN-REGULATION; MICRORNA EXPRESSION; OVARIAN-CANCER; TUMOR-SUPPRESSOR; LUNG-CANCER; PANCREATIC CARCINOGENESIS;
D O I
10.1016/j.gene.2018.06.005
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Ecotropic virus integration site-1 (EVI1) is an oncogenic transcription factor which locus on chromosome 3(3q26.2). Alterations in EVIL functions correspond with poor prognosis in different cancers, underscoring their status for the clinical cancer phenotype. MicroRNAs(MiR)are a class of small non-coding RNA sequences. They post-transcriptionally influence mRNA sequence through imperfect pairing with the 3'-UTR. Moreover, a growing body of studies showed that miRNAs could regulate initiation and progression of human malignancies. Current studies have been described that identifies numerous microRNAs that can be modulated by EVIl. Interestingly, the expression level of EVIl can also be regulated by microRNAs, thus forming a reciprocal link. Recent understanding of the functional roles of EVI1, microRNAs, and their interactions in human cancers are summarized. This review will help to define a relationship between EVI1 and microRNAs in human malignancies and develop novel therapeutic strategies.
引用
收藏
页码:56 / 63
页数:8
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