1. Effects of targeted phosphorylation site mutations in the DNA-PKcs phosphorylation domain on low and high LET radiation sensitivity
- Author
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Akira Fujimori, Hisashi Kitamuta, Ashley M. Romero, Ian M. Cartwright, David J. Chen, Takamitsu A. Kato, Junko Maeda, Tadashi Kamada, Justin J. Bell, Matthew D. Genet, and Yoshihiro Fujii
- Subjects
Cancer Research ,protons ,Point mutation ,Chinese hamster ovary cell ,DNA-protein kinase catalytic subunit ,Bragg peak ,Articles ,Biology ,Bioinformatics ,Ionizing radiation ,high linear energy transfer radiation ,chemistry.chemical_compound ,Oncology ,chemistry ,Biophysics ,Phosphorylation ,Protein kinase A ,heavy ions ,DNA-PKcs ,DNA - Abstract
The present study investigated the effect of targeted mutations in the DNA-dependent protein kinase catalytic subunit and phosphorylation domains on the survival of cells in response to different qualities of ionizing radiation. Mutated Chinese hamster ovary V3 cells were exposed to 500 MeV/nucleon initial energy and 200 keV/μm monoenergetic Fe ions; 290 MeV/nucleon initial energy and average 50 keV/μm spread-out Bragg peak C ions; 70 MeV/nucleon initial energy and 1 keV/μm monoenergetic protons; and 0.663 MeV initial energy and 0.3 keV/μm Cs137 γ radiation. The results demonstrated that sensitivity to high linear energy transfer radiation is increased when both S2056 and T2609 clusters each contain a point mutation or multiple mutations are present in either cluster, whereas the phosphoinositide 3 kinase cluster only requires a single mutation to induce the sensitized phenotype of V3 cells. Additionally, the present study demonstrated that sensitivity to DNA cross-linking damage by cisplatin only requires a single mutation in one of the three clusters and that additional point mutations do not increase cell sensitivity.
- Published
- 2014