Yamashita Kentaro, Nakashima Shigeru, You Fukka, Hayashi Shin-Ichiro, Iwama Toru
Departments of Neurosurgery, Gifu University Graduate School of Medicine, Yanagido, Japan.
Neuropathology. 2009 Feb;29(1):20-4. doi: 10.1111/j.1440-1789.2008.00932.x. Epub 2008 Jun 17.
Malignant gliomas are usually incurable even if adjuvant therapy is delivered after neurosurgical treatment. Therefore, to enhance their radiation-induced apoptosis, it is important to detect the mechanism(s) leading to the death of malignant glioma cells. We report that apoptosis was induced in a time-dependent manner after gamma-radiation and that irradiated U87-MG cells (human glioblastoma cell line) expressed immediate early gene X-1 (IEX-1) with p53. We also document that their apoptotic sensitivity to gamma-radiation was enhanced by the overexpression of IEX-1. Our findings suggest that IEX-1 may represent a new factor for the enhancement of radiation-induced apoptosis of human glioma cells.
恶性胶质瘤通常无法治愈,即便在神经外科治疗后进行辅助治疗也是如此。因此,为了增强其辐射诱导的细胞凋亡,检测导致恶性胶质瘤细胞死亡的机制至关重要。我们报告称,γ射线照射后细胞凋亡呈时间依赖性诱导,且照射后的U87-MG细胞(人胶质母细胞瘤细胞系)与p53共同表达即刻早期基因X-1(IEX-1)。我们还证明,IEX-1的过表达增强了它们对γ射线的凋亡敏感性。我们的研究结果表明,IEX-1可能是增强人胶质瘤细胞辐射诱导凋亡的一个新因素。