Abstract
<div>Abstract<p><b>Purpose:</b> Radiotherapy is commonly used to treat a variety of solid tumors. However, improvements in the therapeutic ratio for several disease sites are sorely needed, leading us to assess molecularly targeted therapeutics as radiosensitizers. The aim of this study was to assess the wee1 kinase inhibitor, MK-1775, for its ability to radiosensitize human tumor cells.</p><p><b>Experimental Design:</b> Human tumor cells derived from lung, breast, and prostate cancers were tested for radiosensitization by MK-1775 using clonogenic survival assays. Both p53 wild-type and p53-defective lines were included. The ability of MK-1775 to abrogate the radiation-induced G<sub>2</sub> block, thereby allowing cells harboring DNA lesions to prematurely progress into mitosis, was determined using flow cytometry and detection of γ-H2AX foci. The <i>in vivo</i> efficacy of the combination of MK-1775 and radiation was assessed by tumor growth delay experiments using a human lung cancer cell line growing as a xenograft tumor in nude mice.</p><p><b>Results:</b> Clonogenic survival analyses indicated that nanomolar concentrations of MK-1775 radiosensitized p53-defective human lung, breast, and prostate cancer cells but not similar lines with wild-type p53. Consistent with its ability to radiosensitize, MK-1775 abrogated the radiation-induced G<sub>2</sub> block in p53-defective cells but not in p53 wild-type lines. MK-1775 also significantly enhanced the antitumor efficacy of radiation <i>in vivo</i> as shown in tumor growth delay studies, again for p53-defective tumors.</p><p><b>Conclusions:</b> These results indicate that p53-defective human tumor cells are significantly radiosensitized by the potent and selective wee1 kinase inhibitor, MK-1775, in both the <i>in vitro</i> and <i>in vivo</i> settings. Taken together, our findings strongly support the clinical evaluation of MK-1775 in combination with radiation. <i>Clin Cancer Res; 17(17); 5638–48. ©2011 AACR</i>.</p></div>
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