Circular RNAs in Cancer - Lessons Learned From microRNAs

被引:107
|
作者
Dragomir, Mihnea [1 ,2 ,3 ]
Calin, George A. [1 ,4 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut, Houston, TX 77030 USA
[2] Iuliu Hatieganu Univ Med & Pharm, Res Ctr Funct Genom Biomed & Translat Med, Cluj Napoca, Romania
[3] Carol Davila Univ Med & Pharm, Fundeni Clin Hosp, Dept Surg, Bucharest, Romania
[4] Univ Texas MD Anderson Canc Ctr, Ctr RNA Interference & Noncoding RNAs, Houston, TX 77030 USA
来源
FRONTIERS IN ONCOLOGY | 2018年 / 8卷
基金
美国国家卫生研究院;
关键词
circular RNA; microRNA; non-coding RNA; cancer; biomarker; CERNA HYPOTHESIS; EXPRESSION; GENE; TRANSCRIPTS; BIOMARKER; ABUNDANT; TARGET; PROGRESSION; CIRCHIPK3; REVEALS;
D O I
10.3389/fonc.2018.00179
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Circular RNAs (circRNA) are RNA molecules built from fragments of linear pre-messenger RNAs and other linear RNA species through a process termed "back-splicing" in which the 3' and 5' ends are joined together giving rise to a covalently uninterrupted loop. circRNAs are not new members of the RNA world; they were first discovered in the early 1990s. The novelty is their abundance in the mammalian cells, as recently thousands of circRNAs were discovered and annotated. The biogenesis of circRNAs is a partially characterized process, regulated by three different mechanisms: exon skipping, intron pairing, and RNA-binding proteins. On the other hand, the function of circRNAs remains largely unknown and only a handful of singular reports describe in detail the biological roles of some circular transcripts. In a very short period of time, numerous circRNAs were associated with various cancer types and were also identified in bodily fluids with the potential of being disease-specific biomarkers. In this review, we briefly describe the biogenesis and function of circRNAs and present the circular transcripts that were more than once reported in literature to be associated with cancer. Finally, we point out some of the difficulties encountered in the study of circRNAs in cancer, as we consider that taking these into account could accelerate and improve our understanding of the biologic and translational use of circRNAs in human diseases.
引用
收藏
页数:12
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