miR-620 promotes tumor radioresistance by targeting 15-hydroxyprostaglandin dehydrogenase (HPGD).

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...

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Main Authors: Huang, X, Taeb, S, Jahangiri, S, Korpela, E, Cadonic, I, Yu, N, Krylov, S, Fokas, E, Boutros, P, Liu, S
Format: Journal article
Language:English
Published: Impact Journals 2015
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author Huang, X
Taeb, S
Jahangiri, S
Korpela, E
Cadonic, I
Yu, N
Krylov, S
Fokas, E
Boutros, P
Liu, S
author_facet Huang, X
Taeb, S
Jahangiri, S
Korpela, E
Cadonic, I
Yu, N
Krylov, S
Fokas, E
Boutros, P
Liu, S
author_sort Huang, X
collection OXFORD
description 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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spelling oxford-uuid:981b4b01-bcdd-452e-a35f-bca104bdabfd2022-03-27T00:04:44ZmiR-620 promotes tumor radioresistance by targeting 15-hydroxyprostaglandin dehydrogenase (HPGD).Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:981b4b01-bcdd-452e-a35f-bca104bdabfdEnglishSymplectic Elements at OxfordImpact Journals2015Huang, XTaeb, SJahangiri, SKorpela, ECadonic, IYu, NKrylov, SFokas, EBoutros, PLiu, SMicroRNA 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.
spellingShingle Huang, X
Taeb, S
Jahangiri, S
Korpela, E
Cadonic, I
Yu, N
Krylov, S
Fokas, E
Boutros, P
Liu, S
miR-620 promotes tumor radioresistance by targeting 15-hydroxyprostaglandin dehydrogenase (HPGD).
title miR-620 promotes tumor radioresistance by targeting 15-hydroxyprostaglandin dehydrogenase (HPGD).
title_full miR-620 promotes tumor radioresistance by targeting 15-hydroxyprostaglandin dehydrogenase (HPGD).
title_fullStr miR-620 promotes tumor radioresistance by targeting 15-hydroxyprostaglandin dehydrogenase (HPGD).
title_full_unstemmed miR-620 promotes tumor radioresistance by targeting 15-hydroxyprostaglandin dehydrogenase (HPGD).
title_short miR-620 promotes tumor radioresistance by targeting 15-hydroxyprostaglandin dehydrogenase (HPGD).
title_sort mir 620 promotes tumor radioresistance by targeting 15 hydroxyprostaglandin dehydrogenase hpgd
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