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Circular RNAs in Cancer - Lessons Learned From microRNAs

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FRONTIERS IN ONCOLOGY
卷 8, 期 -, 页码 -

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FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2018.00179

关键词

circular RNA; microRNA; non-coding RNA; cancer; biomarker

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资金

  1. National Institutes of Health (NIH/NCATS) through the NIH Common Fund, Office of Strategic Coordination (OSC) [UH3TR00943-01]
  2. NIH/NCI grant [1 R01 CA182905-01]
  3. UPR/MDACC Partnership for Excellence in Cancer Research Pilot Project [U54]
  4. Team DOD [CA160445P1]
  5. Ladies Leukemia League grant
  6. CLL Moonshot Flagship project
  7. SINF grant
  8. Estate of C. G. Johnson
  9. POC grant, CANTEMIR, Competitivity Operational Program [35/01.09.2016, MySMIS 103375]

向作者/读者索取更多资源

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.

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