Synergistic radiosensitizing effect of BR101801, a specific DNA-dependent protein kinase inhibitor,in various human solid cancer cells and xenografts |
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Authors: | Jae Hee Lee Byeongwook Jeon Mijeong Park Jimin Ha Soo Jung Kim Mi Kwon Son Seungho Wang Joo Han Lee Youn Kyoung Jeong |
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Institution: | 1. Radiological and Medical Support Center, Korea Institute of Radiological and Medical Sciences, Seoul 01812, Republic of Korea ; 2. Boryung Pharmaceutical, R&D Center, Ansan 15425, Republic of Korea |
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Abstract: | DNA-dependent protein kinase (DNA-PK), an essential component of the non-homologous end-joining (NHEJ) repair pathway, plays an important role in DNA damage repair (DDR). Therefore, DNA-PK inhibition is a promising approach for overcoming radiotherapy or chemotherapy resistance in cancers. In this study, we demonstrated that BR101801, a potent DNA-PK inhibitor, acted as an effective radiosensitizer in various human solid cancer cells and an in vivo xenograft model. Overall, BR101801 strongly elevated ionizing radiation (IR)-induced genomic instability via induction of cell cycle G2/M arrest, autophagic cell death, and impairment of DDR pathway in human solid cancer cells. Interestingly, BR101801 inhibited not only phosphorylation of DNA-PK catalytic subunit in NHEJ factors but also BRCA2 protein level in homologous recombination (HR) factors. In addition, combination BR101801 and IR suppressed tumor growth compared with IR alone by reducing phosphorylation of DNA-PK in human solid cancer xenografts. Our findings suggested that BR101801 is a selective DNA-PK inhibitor with a synergistic radiosensitizing effect in human solid cancers, providing evidence for clinical applications. |
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Keywords: | DNA-PK inhibitor Ionizing radiation radiosensitizer DNA damage repair solid cancer |
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