miR-620 promotes tumor radioresistance by targeting 15-hydroxyprostaglandin dehydrogenase (HPGD)
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Xiaoyong Huang1, Samira Taeb1, Sahar Jahangiri1, Elina Korpela1,2, Ivan Cadonic1, Nancy Yu2, Sergey N. Krylov3, Emmanouil Fokas4, Paul C. Boutros2,5, Stanley K. Liu1,2,6
1Sunnybrook Research Institute, Sunnybrook Health Sciences Centre, Toronto, Canada
2Department of Medical Biophysics, University of Toronto, Toronto, Canada
3Department of Chemistry, York University, Toronto, Canada
4CRUK/MRC Oxford Institute for Radiation Oncology, Gray Laboratories, Department of Oncology, University of Oxford, Oxford, UK
5Ontario Institute for Cancer Research, University of Toronto, Toronto, Canada
6Department of Radiation Oncology, University of Toronto, Toronto, Canada
Stanley K. Liu, e-mail: firstname.lastname@example.org
Keywords: miR-620, radiation resistance, HPGD, PGE2
Received: April 16, 2015 Accepted: May 22, 2015 Published: June 04, 2015
MicroRNA contribute to tumor radiation resistance, which is an important clinical problem, and thus we are interested in identifying and characterizing their function. We demonstrate that miR-620 contributes to radiation resistance in cancer cells by increasing proliferation, and decreasing the G2/M block. We identify the hydroxyprostaglandin dehydrogenase 15-(nicotinamide adenine dinucleotide) (HPGD/15-PGDH) tumor suppressor gene as a direct miR-620 target, which results in increased prostaglandin E2 (PGE2) levels. Furthermore, we show that siRNA targeting of HPGD or administration of exogenous PGE2 recapitulates radioresistance. Targeting of the EP2 receptor that responds to PGE2 using pharmacological or genetic approaches, abrogates radioresistance. Tumor xenograft experiments confirm that miR-620 increases proliferation and tumor radioresistance in vivo. Regulation of PGE2 levels via targeting of HPGD by miR-620 is an innovative manner by which a microRNA can induce radiation resistance.
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Paul C. Boutros
Stanley K. Liu
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