Leith John T, Davis Paul J, Mousa Shaker A, Hercbergs Aleck A
a Rhode Island Nuclear Science Center , Narragansett , RI, USA.
b Albany Medical College , Albany , NY , USA.
Cell Cycle. 2017 Feb 16;16(4):367-373. doi: 10.1080/15384101.2016.1269044. Epub 2017 Jan 23.
We investigated radiosensitization in an untreated basal cell carcinoma (TE.354.T) cell line and post-pretreatment with tetraiodothyroacetic acid (tetrac) X 1 h at 37°C, 0.2 and 2.0 µM tetrac. Radioresistant TE.354.T cells were grown in modified medium containing fibroblast growth factor-2, stem cell factor-1 and a reduced calcium level. We also added reproductively inactivated (30 Gy) "feeder cells" to the medium. The in vitro doubling time was 34.1 h, and the colony forming efficiency was 5.09 percent. These results were therefore suitable for clonogenic radiation survival assessment. The 250 kVp X-ray survival curve of control TE.354.T cells showed linear-quadratic survival parameters of α = 0.201 Gy and β = 0.125 Gy. Tetrac concentrations of either 0.2 or 2.0 µM produced α and β parameters of 2.010 and 0.282 Gy and 2.050 and 0.837 Gy, respectively. The surviving fraction at 2 Gy (SF) for control cells was 0.581, while values for 0.2 and 2.0 µM tetrac were 0.281 and 0.024. The SF data show that tetrac concentrations of 0.2 and 2.0 µM sensitize otherwise radioresistant TE.354.T cells by factors of 2.1 and 24.0, respectively. Thus, radioresistant basal cell carcinoma cells may be radiosensitized pharmacologically by exposure to tetrac.
我们研究了在未经处理的基底细胞癌(TE.354.T)细胞系中以及在37°C下用0.2和2.0μM的四碘甲状腺乙酸(tetrac)预处理1小时后的放射增敏作用。抗辐射的TE.354.T细胞在含有成纤维细胞生长因子-2、干细胞因子-1和降低钙水平的改良培养基中培养。我们还向培养基中添加了经30 Gy辐射使其失去繁殖能力的“饲养细胞”。体外倍增时间为34.1小时,集落形成效率为5.09%。因此,这些结果适用于克隆形成辐射存活评估。对照TE.354.T细胞的250 kVp X射线存活曲线显示线性二次存活参数为α = 0.201 Gy和β = 0.125 Gy。0.2或2.0μM的tetrac浓度分别产生α和β参数为2.010和0.282 Gy以及2.050和0.837 Gy。对照细胞在2 Gy时的存活分数(SF)为0.581,而0.2和2.0μM的tetrac的值分别为0.281和0.024。SF数据表明,0.2和2.0μM的tetrac浓度分别使原本抗辐射的TE.354.T细胞的放射敏感性提高了2.1倍和24.0倍。因此,抗辐射的基底细胞癌细胞可能通过暴露于tetrac而在药理学上实现放射增敏。