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Dopamine receptor D(2) activation suppresses the radiosensitizing effect of aripiprazole via activation of AMPK

Drug repositioning has garnered attention as an alternative strategy to the discovery and development of novel anticancer drug candidates. In this study, we screened 321 FDA‐approved drugs against nonirradiated and irradiated MCF‐7 cells, revealing that aripiprazole, a dopamine receptor D2 (D2R) par...

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Detalles Bibliográficos
Autores principales: Lee, Hyounji, Kang, Seongman, Sonn, Jong Kyung, Lim, Young‐Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722896/
https://www.ncbi.nlm.nih.gov/pubmed/31301124
http://dx.doi.org/10.1002/2211-5463.12699
Descripción
Sumario:Drug repositioning has garnered attention as an alternative strategy to the discovery and development of novel anticancer drug candidates. In this study, we screened 321 FDA‐approved drugs against nonirradiated and irradiated MCF‐7 cells, revealing that aripiprazole, a dopamine receptor D2 (D2R) partial agonist, enhances the radiosensitivity of MCF‐7 cells. Unexpectedly, D2R‐selective antagonist treatment significantly enhanced the radiosensitizing effects of aripiprazole and prevented aripiprazole‐induced 5' adenosine monophosphate‐activated protein kinase (AMPK) phosphorylation. Direct AMPK activation with A769662 treatment blunted the radiosensitizing effects of aripiprazole. These results indicate that aripiprazole has potential as a radiosensitizing drug. Furthermore, prevention of D2R/AMPK activation might enhance these anticancer effects of aripiprazole in breast cancer cells.