For advanced oral squamous cell carcinoma (OSCC), increasing sensitivity to chemotherapy is a major challenge in improving treatment outcomes, and targeting cytoprotective processes that lead to the chemotherapy resistance of cancer cells may be therapeutically promising. Tumor-suppressive microRNAs (miRNAs) can target multiple cancer-promoting genes concurrently and are thus expected to be useful seeds for cancer therapeutics. We revealed that -mediated targeting of multiple cytoprotective process-related genes, including cellular inhibitor of apoptosis protein 1 (), can effectively increase cisplatin (CDDP)-induced cytotoxicity and overcome CDDP resistance in OSCC cells. The combination of topical treatment with ointment and administration of CDDP was synergistically effective against OSCC tumor growth in a xenograft mouse model. Furthermore, the expression of target genes is frequently upregulated in primary OSCC tumors. Our study suggests that reversing -mediated cytoprotective processes activated in cancer cells is a potentially useful strategy to improve CDDP efficacy against advanced OSCC.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9073396PMC
http://dx.doi.org/10.1016/j.omto.2022.02.002DOI Listing

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