Machida H, Matsumoto Y, Shirai M, Kubota N
Department of Radiological Sciences, Ibaraki Prefectural University of Health Sciences, Ami-machi, Ibaraki 300-0394, Japan.
Int J Radiat Biol. 2003 Dec;79(12):973-80. doi: 10.1080/09553000310001626135.
The effects of the heat shock protein 90 (Hsp90) inhibitor geldanamycin (GA) were examined on the radiosensitivity and signal transduction pathways in human tumour cell lines.
Two human cell lines, SQ-5 and DLD-1, derived from lung carcinoma and colon adenocarcinoma, respectively, were incubated for 16 h at 37 degrees C in medium containing 0.2 microM GA. The cells were then irradiated with X-rays and incubated with GA for a further 8 h. Radiation sensitivity was determined by clonogenic assays and protein levels were examined by Western blotting.
GA radiosensitized both cell lines, but potentiated X-ray sensitivity more in SQ-5 than in DLD-1 cells. It was found that GA depleted EGFR and ErbB-2 in DLD-1 cells and depleted only ErbB-2 in SQ-5 cells. GA also reduced the expression of Akt and phosphorylated Akt (pAkt) expression in SQ-5 cells. In addition, the ratio (%) of apoptotic cells and poly [ADP-ribose] polymerase cleavage increased in SQ-5 but not in DLD-1 cells after exposure to GA and X-ray irradiation. The findings suggest that GA enhances the radiation sensitivity of human tumour cells by inhibiting the EGFR signal transduction system and the Akt signalling pathway.
Targeting Hsp90 with GA provides a promising experimental strategy for radiosensitization of carcinoma.
研究热休克蛋白90(Hsp90)抑制剂格尔德霉素(GA)对人肿瘤细胞系放射敏感性及信号转导通路的影响。
分别来源于肺癌和结肠腺癌的两个人类细胞系SQ - 5和DLD - 1,在含有0.2微摩尔GA的培养基中于37℃孵育16小时。然后对细胞进行X射线照射,并继续与GA孵育8小时。通过克隆形成试验测定放射敏感性,通过蛋白质印迹法检测蛋白质水平。
GA使两个细胞系均对放射增敏,但对SQ - 5细胞的X射线敏感性增强作用比对DLD - 1细胞更强。发现GA使DLD - 1细胞中的表皮生长因子受体(EGFR)和ErbB - 2减少,而仅使SQ - 5细胞中的ErbB - 2减少。GA还降低了SQ - 5细胞中Akt及磷酸化Akt(pAkt)的表达。此外,在暴露于GA和X射线照射后,SQ - 5细胞中凋亡细胞的比例(%)及聚[ADP - 核糖]聚合酶的裂解增加,而DLD - 1细胞中未增加。这些发现表明GA通过抑制EGFR信号转导系统和Akt信号通路增强人肿瘤细胞的放射敏感性。
用GA靶向Hsp90为癌症的放射增敏提供了一种有前景的实验策略。