Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8223914 | International Journal of Radiation Oncology*Biology*Physics | 2012 | 8 Pages |
Abstract
TS shRNA produced less cytotoxicity than FdUrd but was equally effective at radiosensitizing tumor cells. Thus, the inhibitory effect of FdUrd on TS alone is sufficient to elicit radiosensitization with FdUrd, but it only partially explains FdUrd-mediated cytotoxicity and cell cycle inhibition. The increase in DNA mismatches after TS shRNA or FdUrd supports a causal and sufficient role for the depletion of dTTP thymidine triphosphate and consequent DNA mismatches underlying radiosensitization. Importantly, shRNA suppression of TS avoids FP-mediated TS elevation and its negative prognostic role. These studies support the further exploration of TS suppression as a novel radiosensitizing strategy.
Related Topics
Physical Sciences and Engineering
Physics and Astronomy
Radiation
Authors
Sheryl A. PhD, Kristin S. Cooper, Sudha MSc, Mikhail A. PhD, Donna S. PhD,