Abstract

MicroRNAs (miRNAs) regulate key biological processes, and their aberrant expression has been related to cancer development. Photodynamic therapy (PDT) has emerged as one of the most promising modalities for cancer treatment. However, the application of PDT has been limited to superficially localized human cancerous and precancerous lesions. To increase the usefulness of both PDT and miRNAs in cancer therapy, this study investigated whether apoptosis-related miRNA expression is influenced by PDT in oral cancer and whether miRNAs can enhance PDT efficacy. To achieve this goal, we performed a miRNA array-based comparison of apoptosis-related miRNA expression patterns following PDT using pheophorbide a (Pa) as a photosensitizer. After Pa-PDT, 13.1% of the miRNAs were down-regulated, and 16.7% of the miRNAs were up-regulated. Representative miRNAs were selected according to expression difference: miR-9-5p, miR-32-5p, miR-143-3p, miR-145-5p, miR-192-5p, miR-193a-5p, miR-204-5p, miR-212-3p, miR-338-3p, and miR-451a. Among them, only miR-145-5p showed the consistent reduction repeatedly in all cell lines after Pa-PDT. Further, the combined treatment of a miR-145-5p mimic and Pa-PDT increased phototoxicity, reactive oxygen species generation, and apoptotic cell death, suggesting that miRNAs expression could be a useful marker for enhancing the therapeutic effect of Pa-PDT. This study will provide a promising strategy for introducing miRNA as cancer therapy.

Highlights

  • MicroRNAs are a class of highlyconserved, short, non-coding RNAs that have emerged as important mediators of translational control

  • To increase the usefulness of both Photodynamic therapy (PDT) and miRNAs in cancer therapy, this study investigated whether apoptosis-related miRNA expression is influenced by PDT in oral cancer and whether miRNAs can enhance PDT efficacy

  • To investigate whether miRNA expression is influenced by pheophorbide a (Pa)-PDT, 84 apoptosis-related miRNAs were profiled in YD1OB oral squamous cell carcinoma (OSCC) cells using human microRNA arrays and quantitative PCR analysis

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Summary

Introduction

MicroRNAs (miRNAs, miRs) are a class of highlyconserved, short, non-coding RNAs that have emerged as important mediators of translational control. MRNA cleavage or a combination of the two, miRNAs regulate the expression of their target genes, mostly via direct targeting of the 3’-untranslated region (UTR) of mRNAs [1,2,3]. MiRNAs regulate a wide range of biological processes, including apoptosis, differentiation and cell proliferation [4, 5]. Aberrant expression and function of miRNAs have been reported in many types of cancers [6, 7]. MiRNAs might enhance chemosensitivity and radiosensitivity in human cancer therapy [9, 10]

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