Shin Sun Hye, Yoon Mi Jin, Kim Mira, Kim Jong-Il, Lee Su-Jae, Lee Yun-Sil, Bae Sangwoo
Laboratory of Radiation Effect, Korea Institute of Radiological and Medical Sciences, Seoul 139-706, Korea.
Oncol Rep. 2007 Jan;17(1):209-16.
Selenium has been associated with anticancer activity by affecting multiple cellular processes. We reasoned that the simultaneous modulation of multiple radioresponse regulators by selenium should increase radiosensitivity if selenium is combined with radiation in cancer therapy. Therefore, we explored the possibility of whether we could obtain an enhancement of radiosensitivity by the combination of selenium and ionizing radiation. We used two human lung cancer cell lines, NCI-H460 and H1299, as well as a human diploid lung fibroblast, WI-38, as the normal cell counterpart. The combined treatment of the cancer cell lines with Seleno-methionine and ionizing radiation resulted in increased cell killing as assessed by clonogenic survival assay whereas it had little effect on the normal diploid WI-38 cells. The increased radiosensitivity in the cancer cells was correlated with the attenuation of the key proteins involved in either cell survival signaling [Akt, EGFR (epidermal growth factor receptor), ErbB2 and Raf1] or DNA damage response (Mre11, Rad50, Nbs1, Ku80, 53BP1 and DNAPK). The attenuation of the proteins by the selenium compound was possibly caused by the effect on transcription and on protein stability since selenium treatment decreased both the RNA transcript and the protein stability of EGFR and DNAPK. By contrast, Seleno-L-methionine had no effect on the protein profile of a normal diploid fibroblast which is consistent with an intact radiosensitivity. These data provide possible clinical applications, as selenium selectively enhanced the radiosensitivity of the tumor cells whereas that of the normal cells was unaffected. Moreover, the selective decrease of cell proliferation signaling in tumor cells but not in normal cells should facilitate the repopulation of normal cells required for healing during radiation therapy. On the whole, the results suggest that the cancer preventive activity of selenium can be combined with ionizing radiation to improve the control of lung cancer.
硒通过影响多种细胞过程而具有抗癌活性。我们推测,如果在癌症治疗中将硒与放疗相结合,硒对多种放射反应调节因子的同时调节应能提高放射敏感性。因此,我们探讨了硒与电离辐射联合使用是否能增强放射敏感性的可能性。我们使用了两种人肺癌细胞系NCI-H460和H1299,以及一种人二倍体肺成纤维细胞WI-38作为正常细胞对照。用硒代蛋氨酸和电离辐射联合处理癌细胞系,通过克隆形成存活试验评估,结果显示细胞杀伤增加,而对正常二倍体WI-38细胞几乎没有影响。癌细胞放射敏感性的增加与细胞存活信号通路(Akt、表皮生长因子受体EGFR、ErbB2和Raf1)或DNA损伤反应(Mre11、Rad50、Nbs1、Ku80、53BP1和DNA依赖蛋白激酶DNAPK)中关键蛋白的减弱有关。硒化合物对这些蛋白的减弱可能是由于对转录和蛋白稳定性的影响,因为硒处理降低了EGFR和DNAPK的RNA转录本和蛋白稳定性。相比之下,硒代-L-蛋氨酸对正常二倍体成纤维细胞的蛋白谱没有影响,这与完整的放射敏感性一致。这些数据提供了可能的临床应用,因为硒选择性地增强了肿瘤细胞的放射敏感性,而正常细胞的放射敏感性未受影响。此外,肿瘤细胞而非正常细胞中细胞增殖信号的选择性降低应有助于放疗期间愈合所需的正常细胞的再增殖。总体而言,结果表明硒的癌症预防活性可与电离辐射相结合,以改善肺癌的控制。