Lomonaco Stephanie L, Finniss Susan, Xiang Cunli, Decarvalho Ana, Umansky Felix, Kalkanis Steven N, Mikkelsen Tom, Brodie Chaya
Department of Neurosurgery, William and Karen Davidson Laboratory of Cell Signaling and Tumorigenesis, Hermelin Brain Tumor Center, Henry Ford Hospital, Detroit, MI 48202, USA
Int J Cancer. 2009 Aug 1;125(3):717-22. doi: 10.1002/ijc.24402.
Malignant gliomas are characterized by a short median survival which is largely impacted by the resistance of these tumors tochemo- and radiotherapy. Recent studies suggest that a small subpopulation of cancer stem cells, which are highly resistant to gamma-radiation, has the capacity to repopulate the tumors and contribute to their malignant progression. gamma-radiation activates the process of autophagy and inhibition of this process increases the radiosensitivity of glioma cells; however, the role of autophagy in the resistance of glioma stem cells (GSCs) to radiation has not been yet reported. In this study we examined the induction of autophagy by gamma-radiation in CD133+ GSCs. Irradiation of CD133+ cells induced autophagy within 24-48 hr and slightly decreased the viability of the cells. gamma-radiation induced a larger degree of autophagy in the CD133+ cells as compared with CD133- cells and the CD133+ cells expressed higher levels of the autophagy-related proteins LC3, ATG5 and ATG12. The autophagy inhibitor bafilomycin A1 and silencing of ATG5 and beclin1 sensitized the CD133+ cells to gamma-radiation and significantly decreased the viability of the irradiated cells and their ability to form neurospheres. Collectively, these results indicate that the induction of autophagy contributes to the radioresistance of these cells and autophagy inhibitors may be employed to increase the sensitivity of CD133+ GSCs to gamma-radiation.
恶性胶质瘤的特征是中位生存期短,这在很大程度上受到这些肿瘤对化疗和放疗耐药性的影响。最近的研究表明,一小部分对γ射线高度耐药的癌症干细胞有能力使肿瘤重新增殖并促进其恶性进展。γ射线激活自噬过程,抑制这一过程可增加胶质瘤细胞的放射敏感性;然而,自噬在胶质瘤干细胞(GSCs)对辐射的耐药性中的作用尚未见报道。在本研究中,我们检测了γ射线对CD133+ GSCs自噬的诱导作用。照射CD133+细胞在24 - 48小时内诱导自噬,并使细胞活力略有下降。与CD133-细胞相比,γ射线在CD133+细胞中诱导了更大程度的自噬,且CD133+细胞表达更高水平的自噬相关蛋白LC3、ATG5和ATG12。自噬抑制剂巴弗洛霉素A1以及ATG5和贝林1的沉默使CD133+细胞对γ射线敏感,并显著降低了照射细胞的活力及其形成神经球的能力。总的来说,这些结果表明自噬的诱导有助于这些细胞的放射抗性,自噬抑制剂可用于提高CD133+ GSCs对γ射线的敏感性。