Department of Radiation Oncology, Gunma University Graduate School of Medicine, Gunma, Japan.
J Radiat Res. 2012 Jul;53(4):545-50. doi: 10.1093/jrr/rrs012.
The purpose of this study is to clarify the effect of a heat shock protein 90 inhibitor, 17-allylamino-17-demethoxygeldanamycin (17-AAG), in combination with X-rays or carbon-ion beams on cell killing in human oral squamous cell carcinoma LMF4 cells. Cell survival was measured by colony formation assay. Cell-cycle distribution was analyzed by flow cytometry. Expression of DNA repair-related proteins was investigated by western blotting. The results showed 17-AAG to have synergistic effects on cell lethality with X-rays, but not with carbon-ion beams. The 17-AAG decreased G(2)/M arrest induced by X-rays, but not by carbon-ion beams. Both X-ray and carbon-ion irradiation up-regulated expression of non-homologous end-joining-associated proteins, Ku70 and Ku80, but 17-AAG inhibited only X-ray-induced up-regulation of these proteins. These results show that 17-AAG with X-rays releases G(2)/M phase arrest; cells carrying misrepaired DNA damage then move on to the G(1) phase. We demonstrate, for the first time, that the radiosensitization effect of 17-AAG is not seen with carbon-ion beams because 17-AAG does not affect these changes.
本研究旨在阐明热休克蛋白 90 抑制剂 17- 烯丙基-17- 脱甲氧基格尔德霉素(17-AAG)与 X 射线或碳离子束联合应用对人口腔鳞状细胞癌细胞株 LMF4 细胞杀伤作用的影响。采用集落形成实验检测细胞存活情况,流式细胞术分析细胞周期分布,Western blot 检测 DNA 修复相关蛋白的表达。结果显示,17-AAG 与 X 射线具有协同细胞致死作用,但与碳离子束无协同作用。17-AAG 降低 X 射线诱导的 G2/M 期阻滞,但不降低碳离子束诱导的 G2/M 期阻滞。X 射线和碳离子照射均可上调非同源末端连接相关蛋白 Ku70 和 Ku80 的表达,而 17-AAG 仅抑制 X 射线诱导的这些蛋白的上调。这些结果表明,17-AAG 与 X 射线联合应用可解除 G2/M 期阻滞;携带错误修复的 DNA 损伤的细胞随后进入 G1 期。我们首次证明,17-AAG 对碳离子束的放射增敏作用不存在,因为 17-AAG 不影响这些变化。