Abstract
Emerging evidences have demonstrated that miRNAs could directly or indirectly regulate drug resistance through modulation of epithelial-to-mesenchymal transition (EMT) and cancer stem cells (CSCs) characteristics. Several miRNAs including let-7, miR-15/16, miR-200, miR-34a, miR-143/145, miR-21, miR-155, miR-197, and miR-221/222 have been found to play crucial roles in the control of drug resistance, EMT, and CSCs in pancreatic and prostate cancers. Therefore, targeting these miRNAs by synthetic agents, nutraceuticals, or synthetic oligonucleotide delivery could become a promising approach for overcoming drug resistance, reversal of EMT, and elimination of CSCs, which would likely lead successful treatment of outcome in patients diagnosed with pancreatic and prostate cancers.
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Acknowledgements
The authors’ work cited in this review article was funded by grants from the National Cancer Institute, NIH (5R01CA083695, 5R01CA108535, 5R01CA131151, 5R01CA132794, 5R01CA154321, and 1R01CA164318 awarded to FHS). We also thank Puschelberg and Guido foundations for their generous financial contribution.
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Li, Y., Kong, D., Ahmad, A., Bao, B., Sarkar, F.H. (2014). MicroRNA Targeted Therapy for Overcoming Drug Resistance, Reversal of EMT and Elimination of Cancer Stem Cells in Prostate and Pancreatic Cancer. In: Sarkar, F. (eds) MicroRNA Targeted Cancer Therapy. Springer, Cham. https://doi.org/10.1007/978-3-319-05134-5_12
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DOI: https://doi.org/10.1007/978-3-319-05134-5_12
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