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The Role of Circular RNAs in DNA Damage Response and Repair

Journal

CANCERS
Volume 13, Issue 21, Pages -

Publisher

MDPI
DOI: 10.3390/cancers13215352

Keywords

circRNA; double-strand breaks (DSB); DNA damage response and repair (DDRR); tumorigenesis

Categories

Funding

  1. Hellenic Foundation for Research and Innovation (HFRI) [775, 3782]
  2. General Secretariat for Research and Innovation (GSRI) [775, 3782]
  3. National Public Investment Program of the Ministry of Development and Investment/General Secretariat for Research and Technology [2020SE01300001]
  4. European Union (European Social Fund-ESF) through the Operational Program Human Resources Development, Education and Lifelong Learning [MIS-5033021]

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The text highlights the underappreciated role of non-coding RNAs, particularly circular RNAs, in the DNA damage response and repair network. It emphasizes the importance of further research in this area for potential therapeutic opportunities, while also acknowledging the lack of detailed understanding of the properties and functional roles of these molecules.
The role of non-coding RNA, and particularly of circular RNA, in the DNA damage response and repair network is underappreciated. Given the vital role of this network in preserving the genomic integrity and consequently cellular homeostasis, the constantly increasing numbers of discovered circular RNAs and the increasing implication of these molecules in the function of this network unravel a new important field that may open new therapeutic opportunities, but also require detailed investigation. Circular RNAs (circRNA) comprise a distinct class of non-coding RNAs that are abundantly expressed in the cell. CircRNAs have the capacity to regulate gene expression by interacting with regulatory proteins and/or other classes of RNAs. While a vast number of circRNAs have been discovered, the majority still remains poorly characterized. Particularly, there is no detailed information on the identity and functional role of circRNAs that are transcribed from genes encoding components of the DNA damage response and repair (DDRR) network. In this article, we not only review the available published information on DDRR-related circRNAs, but also conduct a bioinformatic analysis on data obtained from public repositories to uncover deposited, yet uncharacterized circRNAs derived from components of the DDRR network. Finally, we interrogate for potential targets that are regulated by this class of molecules and look into potential functional implications.

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