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Authors Long L, Zhang X, Bai J, Li Y, Wang X, Zhou Y
Received 20 December 2018
Accepted for publication 15 April 2019
Published 13 May 2019 Volume 2019:11 Pages 4413—4424
DOI https://doi.org/10.2147/CMAR.S198966
Checked for plagiarism Yes
Review by Single-blind
Peer reviewers approved by Dr Colin Mak
Peer reviewer comments 2
Editor who approved publication: Dr Chien-Feng Li
Abstract: Lung
cancer is the most prevalent and deadly malignancy. Radiotherapy is a major
treatment modality for lung cancer. Nevertheless, radioresistance poses a
daunting challenge that largely limits the efficacy of radiotherapy. There is a
pressing need for deciphering molecular mechanisms underlying radioresistance
and elucidating novel therapeutic targets for individualized radiotherapy.
MicroRNAs are categorized as small noncoding RNAs that modulate target-gene
expression posttranscriptionally and are implicated in carcinogenesis and
cancer resistance to treatment. Overwhelming evidence has unraveled that
tissue-specific miRNAs are essential for regulation of the radiosensitivity in
lung cancer cells through a complex interaction with multiple biological
processes and radiation-induced pathways. Moreover, exosome-derived miRNAs are
a novel horizon in lung cancer treatment in which exosomal miRNAs act as
potential diagnostic and therapeutic biomarkers of radiotherapy. In the present
review, we discuss the mediation of key biological processes and signaling
pathways by tissue-specific miRNAs in lung cancer radiotherapy. Additionally,
we provide new insight into the potential significance of exosomal miRNAs in
radiation response. Lastly, we highlight miRNAs as promising predictors and
therapeutic targets to tailor personalized lung cancer radiotherapy.
Keywords: lung
cancer, microRNAs, exosome, radioresistance, personalized radiotherapy
