Non-coding RNAs in cellular response to ionizing radiation
Letter to the Editor

Non-coding RNAs in cellular response to ionizing radiation

Andrea Borghini, Maria Grazia Andreassi

CNR Institute of Clinical Physiology, Pisa, Italy

Correspondence to: Dr. Maria Grazia Andreassi. CNR Institute of Clinical Physiology, Via Moruzzi 1, 56124 Pisa, Italy. Email: mariagrazia.andreassi@ifc.cnr.it.

Response to: Jimenez-Mateos EM, Henshall DC. Could miR-134 be a marker of ionizing radiation toxicity? Non-coding RNA Investig 2018;2:24.


Received: 14 June 2018; Accepted: 26 June 2018; Published: 06 July 2018.

doi: 10.21037/ncri.2018.06.10


The evaluation of the health effects of low-dose ionizing radiation (IR) has always been a fundamental topic of scientific research. Health effects involve not only cancer, but also other common diseases (including cardiovascular diseases and neurocognitive impairment) and heritable mutations that can be transmitted to offspring, increasing the risk of diseases in future generations. Therefore, continued research is needed to better improve our understanding of the biological and, consequently, health effects of low levels of IR.

With the development and application of high-throughput technologies, there is a growing interest in non-coding RNAs (ncRNA) as key new players in the regulation of disease-relevant genes (1). Consequently, ncRNAs represent crucial and attractive biological markers for elucidating the molecular mechanisms underlying the onset of disease from low-level IR exposure (Figure 1).

Figure 1 Schematic simplified representation of transcripted RNAs and their potential influence in cellular response to ionizing radiation.

ncRNAs include small non-coding RNAs (e.g., microRNA), long non-coding RNAs (lncRNA) and circular RNAs (circRNA), a specific subtype of lncRNAs that form circular structures. Of the small ncRNA, miRNAs are the most extensively studied in radiobiological response (2).

Generally, most miRNA-related research has been conducted on cellular and animal models, especially after exposure to high doses of IR (2).

Recently, our group also revealed the dysregulation of specific circulating miRNA profiles in interventional cardiologists, who accumulate significant lifetime IR exposure as a result of procedures they undertake (3).

As detailed in the elegant editorial by Jimenez-Mateos and Henshall (4), the altered expression of the brain-specific miRNA-134 in interventional cardiologists supports a direct effect of radiation on the molecular regulatory mechanisms modulating key functions in the brain, which might contribute to the development of radiation-induced late cognitive impairment.

These results also underline the importance of further exploration about the role of ncRNAs in cellular response to IR. Recently, important regulatory functions have been described for lncRNAs and circRNAs, which can influence gene expression through many ways, including epigenetic regulation, transcriptional activation and posttranscriptional modification of mRNA.

LncRNAs are non-protein coding transcripts that are longer than 200 nucleotides and account for a large proportion of the non-coding transcriptome (5).

CircRNAs are instead a novel type of RNA that is generated from exonic or intronic sequences and shows tissue-specific expression. Because circRNAs form a covalently closed continuous loop, they are free of exonuclease-mediated degradation and, in turn, more stable than linear RNAs (6).

Additionally, both lncRNAs and circRNAs can serve as miRNA sponges and regulate mRNA expression in a complicated and intertwined network.

However, whether and how exposure to low-dose IR affects lncRNA and circRNA expression is still poorly investigated.

Until now, few studies explored the role of lncRNAs in the response to low-dose radiation in human cell lines (7,8). Interestingly, dysregulated lncRNAs were predicted to target genes associated with fundamental cellular processes (e.g., cell signaling, programmed cell death) as well as to directly affect locus-specific methylation associated with silencing of gene expression (7,8). More recently, the increased levels of lncRNA particle following low-dose irradiation has been shown to regulate transcription of its neighboring genes (9).

To date, only one study identified circRNAs as potential responders to IR in HUVEC cells (10). Microarray circRNA profiling and next-generation sequencing technology revealed that circRNA expression was altered by low and medium dose exposure and sourced predominantly from genes influencing the p53 pathway. In particular, two specific circRNAs (circRNA KIRKOS-71 and KIRKOS-73) transcribed from the WWOX tumor suppressor gene (a p53 regulator) resulted dysregulated after irradiation (10).

Despite these preliminary evidences, however, the association between IR exposure and ncRNAs dysregulation remain largely uncharacterized.

Understanding the functions and regulatory mechanisms of these RNA molecules in the cellular radiation response is a priority research field to be intensively explored in next years.


Acknowledgements

None.


Footnote

Conflicts of Interest: The authors have no conflicts of interest to declare.


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doi: 10.21037/ncri.2018.06.10
Cite this article as: Borghini A, Andreassi MG. Non-coding RNAs in cellular response to ionizing radiation. Non-coding RNA Investig 2018;2:42.