Pietras Alexander, Katz Amanda M, Ekström Elin J, Wee Boyoung, Halliday John J, Pitter Kenneth L, Werbeck Jillian L, Amankulor Nduka M, Huse Jason T, Holland Eric C
Human Biology Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA; Alvord Brain Tumor Center, University of Washington, Seattle, WA 98104, USA; Cancer Biology and Genetics Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA; Brain Tumor Center, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Cancer Biology and Genetics Program, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA; Brain Tumor Center, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Cell Stem Cell. 2014 Mar 6;14(3):357-69. doi: 10.1016/j.stem.2014.01.005.
Stem-like glioma cells reside within a perivascular niche and display hallmark radiation resistance. An understanding of the mechanisms underlying these properties will be vital for the development of effective therapies. Here, we show that the stem cell marker CD44 promotes cancer stem cell phenotypes and radiation resistance. In a mouse model of glioma, Cd44(-/-) and Cd44(+/-) animals showed improved survival compared to controls. The CD44 ligand osteopontin shared a perivascular expression pattern with CD44 and promoted glioma stem cell-like phenotypes. These effects were mediated via the γ-secretase-regulated intracellular domain of CD44, which promoted aggressive glioma growth in vivo and stem cell-like phenotypes via CBP/p300-dependent enhancement of HIF-2α activity. In human glioblastoma multiforme, expression of CD44 correlated with hypoxia-induced gene signatures and poor survival. Altogether, these data suggest that in the glioma perivascular niche, osteopontin promotes stem cell-like properties and radiation resistance in adjacent tumor cells via activation of CD44 signaling.
干细胞样胶质瘤细胞存在于血管周围微环境中,并表现出典型的放射抗性。了解这些特性背后的机制对于开发有效的治疗方法至关重要。在这里,我们表明干细胞标志物CD44促进癌症干细胞表型和放射抗性。在胶质瘤小鼠模型中,与对照组相比,Cd44(-/-)和Cd44(+/-)动物的生存期有所延长。CD44配体骨桥蛋白与CD44具有共同的血管周围表达模式,并促进胶质瘤干细胞样表型。这些作用是通过CD44的γ-分泌酶调节的胞内结构域介导的,该结构域通过CBP/p300依赖的HIF-2α活性增强促进体内侵袭性胶质瘤生长和干细胞样表型。在多形性胶质母细胞瘤中,CD44的表达与缺氧诱导的基因特征和不良预后相关。总之,这些数据表明,在胶质瘤血管周围微环境中,骨桥蛋白通过激活CD44信号通路促进相邻肿瘤细胞的干细胞样特性和放射抗性。