Hostname: page-component-78c5997874-g7gxr Total loading time: 0 Render date: 2024-11-14T03:22:32.315Z Has data issue: false hasContentIssue false
  • English
  • Français

Circulating microRNAs: are they indicators for the prediction of radiotherapy-induced normal tissue injury

Published online by Cambridge University Press:  06 June 2016

Ahmad Shahabi ,
Hossein Salehi ,
Mohammad Panahi  and
Mohammad Halimi
Ahmad Shahabi
Affiliation:
Department of Biology, Babol Branch, Islamic Azad University, Babol, Iran
Hossein Salehi
Affiliation:
Department of Biology, Babol Branch, Islamic Azad University, Babol, Iran
Mohammad Panahi
Affiliation:
Faculty of chemistry, Kharazmi University, Tehran, Iran
Mohammad Halimi*
Affiliation:
Department of Biology, Babol Branch, Islamic Azad University, Babol, Iran
*
Correspondence to: Mohammad Halimi, Islamic Azad University Babol Branch, Babol, Mazandaran, Islamic Republic of Iran, Tel: +98-9112174966. E-mail: [email protected]
Rights & Permissions [Opens in a new window]

Abstract

An abstract is not available for this content. As you have access to this content, full HTML content is provided on this page. A PDF of this content is also available in through the ‘Save PDF’ action button.
Type
Letters to the Editor
Information
Journal of Radiotherapy in Practice , Volume 16 , Issue 4 , December 2017 , pp. 476 - 477
Check for updates
Copyright
© Cambridge University Press 2016 

Dear Editor,

A large number of patients develop normal tissue injury following radiotherapy and this problem is becoming an important survivorship issue as the rate of curing cancer is increasing.Reference Kerns, Ostrer and Rosenstein 1 Although there is no biomarker in clinical use for identification of patients that would develop adverse effects following radiotherapy, two proteins including TGF-β1 and IL-6 have been shown to be involved in radiation-induced normal tissue toxicity and have been used as biomarkers for the prediction of radiotherapy-induced adverse effects in several independent studies. Different expressions of these proteins may partly explain the individual differences in radiotherapy toxicity observed in patients.

MicroRNAs (miRNAs) are short RNA molecules that regulate gene expression post-transcriptionally by binding to 3' or 5' untranslated region of protein coding RNAs and leading their degradation or repressing their translation.Reference Winter, Jung, Keller, Gregory and Diederichs 2 These noncoding RNA molecules tend to have noteworthy roles in a variety of cellular processes, especially in cellular responses to ionising radiation.Reference Halimi, Asghari, Sariri, Moslemi and Parsian 3 , Reference Mao, Liu, Zhang, Di and Sun 4 miRNAs contribute to the regulation of expression of TGF-β1 and IL-6 too. As there are several cross-talk between miRNAs and these proteins, different expressions of their related miRNAs in low-risk and high-risk patients would not be unexpected. Accordingly, it appear that miR-21 would increase, whereas miR-133, miR-590, let-7a, miR-187 and miR-223 would decrease in patients at risk of developing normal tissue toxicity following radiotherapy (Figure 1). Considering the point that miRNAs could release into the blood, different circulating levels of these miRNAs in low-risk and high-risk patients could be expected. This can be worthwhile for the prediction of radiotherapy-induced normal tissue injury due to the high stability of miRNAs in blood and their easy quantification by quantitative real-time PCR and other methods.

Figure 1 A simplified working model for potential microRNAs (miRNAs) involved in radiation-induced normal tissue injury and their targets. Orange colours show miRNAs and proteins that are expected to upregulate in people who would develop normal tissue injury following radiotherapy. Blue colours show miRNAs and proteins that are expected to downregulate in people who would develop normal tissue injury following radiotherapy. Abbreviations: STAT3, signal transducer and activator of transcription 3; Smad3, Mothers against decapentaplegic homolog 3 or SMAD family member 3; IκBζ, inhibitor of nuclear factor kappa B zeta; IL-6, Interleukin 6; TGF-β1, Transforming growth factor beta 1.

Sincerely,

Mohammad Halimi

Acknowledgements

This work was supported by Islamic Azad University, Babol branch.

Conflicts of Interest

None.

Footnotes

†

These authors contributed equally to this work.

References

1. Kerns, S L, Ostrer, H, Rosenstein, B S. Radiogenomics: using genetics to identify cancer patients at risk for development of adverse effects following radiotherapy. Cancer Discov 2014; 4: 155–165.Google Scholar
2. Winter, J, Jung, S, Keller, S, Gregory, R I, Diederichs, S. Many roads to maturity: microRNA biogenesis pathways and their regulation. Nat Cell Biol 2009; 11: 228–234.Google Scholar
3. Halimi, M, Asghari, S M, Sariri, R, Moslemi, D, Parsian, H. Cellular response to ionizing radiation: a microRNA story. Int J Mol Cell Med 2013; 1: 1–7.Google Scholar
4. Mao, A, Liu, Y, Zhang, H, Di, C, Sun, C. MicroRNA expression and biogenesis in cellular response to ionizing radiation. DNA Cell Biol 2014;10: 667–679.Google Scholar
Figure 0

Figure 1 A simplified working model for potential microRNAs (miRNAs) involved in radiation-induced normal tissue injury and their targets. Orange colours show miRNAs and proteins that are expected to upregulate in people who would develop normal tissue injury following radiotherapy. Blue colours show miRNAs and proteins that are expected to downregulate in people who would develop normal tissue injury following radiotherapy. Abbreviations: STAT3, signal transducer and activator of transcription 3; Smad3, Mothers against decapentaplegic homolog 3 or SMAD family member 3; IκBζ, inhibitor of nuclear factor kappa B zeta; IL-6, Interleukin 6; TGF-β1, Transforming growth factor beta 1.