Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016 Aug 18:7:355.
doi: 10.3389/fphys.2016.00355. eCollection 2016.

Circular RNAs as Promising Biomarkers: A Mini-Review

Affiliations
Review

Circular RNAs as Promising Biomarkers: A Mini-Review

Nadiah Abu et al. Front Physiol. .

Abstract

The interest in circular RNAs has resurfaced in the past few years. What was considered as "junk" for nearly two decades is now one of the most interesting molecules. Circular RNAs are non-coding RNAs that are formed by back-splicing events and have covalently closed loops with no poly-adenylated tails. The regulation of circular RNAs is distinctive and they are selectively abundant in different types of tissues. Based on the current knowledge of circular RNAs, these molecules have the potential to be the "next big thing" especially as biomarkers for different diseases. This mini-review attempts to concisely look at the biology of circular RNAs, the putative functional activities, the prevalence of circular RNAs, and the possible role of circular RNA as biomarkers for diagnosis or measuring drug response.

Keywords: biomarker; cancer; circular RNAs; targeted therapies.

PubMed Disclaimer

Figures

Figure 1
Figure 1
A schematic proposition on how circular RNAs function and are transported around the cellular system. There are many possibilities to the function of circular RNAs such as sponging miRNA, binding to RNA binding proteins, being packaged into extracellular vesicles and exosomes and assisting in protein translation.

References

    1. Ahmed I., Karedath T., Andrews S. S., Al-Azwani I. K., Ali Mohamoud Y., Querleu D., et al. . (2016). Altered expression pattern of circular RNAs in primary and metastatic sites of epithelial ovarian carcinoma. Oncotarget. [Epub ahead of print]. 10.18632/oncotarget.8917. - DOI - PMC - PubMed
    1. Bachmayr-Heyda A., Reiner A. T., Auer K., Sukhbaatar N., Aust S., Bachleitner-Hofmann T., et al. . (2015). Correlation of circular RNA abundance with proliferation – exemplified with colorectal and ovarian cancer, idiopathic lung fibrosis, and normal human tissues. Sci. Rep. 5:8057. 10.1038/srep08057 - DOI - PMC - PubMed
    1. Baran J., Baj-Krzyworzeka M., Weglarczyk K., Szatanek R., Zembala M., Barbasz J., et al. . (2010). Circulating tumour-derived microvesicles in plasma of gastric cancer patients. Cancer Immunol. Immunother. 59, 841–850. 10.1007/s00262-009-0808-2 - DOI - PMC - PubMed
    1. Boeckel J.-N., Jaé N., Heumüller A. W., Chen W., Boon R. A., Stellos K., et al. . (2015). Identification and characterization of hypoxia-regulated endothelial circular RNA. Circ. Res. 117, 884–890. 10.1161/CIRCRESAHA.115.306319 - DOI - PubMed
    1. Burd C. E., Jeck W. R., Liu Y., Sanoff H. K., Wang Z., Sharpless N. E. (2010). Expression of linear and novel circular forms of an INK4/ARF-associated non-coding RNA correlates with atherosclerosis risk. PLoS Genet. 6:e1001233. 10.1371/journal.pgen.1001233 - DOI - PMC - PubMed

LinkOut - more resources