Data from Microenvironmental Regulation of Glioblastoma Radioresponse

Abstract

<div>Abstract<p><b>Purpose:</b> Brain tumor xenografts initiated from human glioblastoma (GBM) stem-like cells (TSC) simulate the biological characteristics of GBMs <i>in situ</i>. Therefore, to determine whether the brain microenvironment affects the intrinsic radiosensitivity of GBM cells, we compared the radioresponse of GBM TSCs grown <i>in vitro</i> and as brain tumor xenografts.</p><p><b>Experimental Design:</b> As indicators of DNA double-strand breaks (DSB), γH2AX, and 53BP1 foci were defined after irradiation of 2 GBM TSC lines grown <i>in vitro</i> and as orthotopic xenografts in nude mice. Microarray analysis was conducted to compare gene expression patterns under each growth condition.</p><p><b>Results:</b> Dispersal of radiation-induced γH2AX and 53BP1 foci was faster in the tumor cells grown as orthotopic xenografts compared with cells irradiated <i>in vitro</i>. In addition, cells irradiated <i>in vivo</i> were approximately 3-fold less susceptible to foci induction as compared with cells grown <i>in vitro</i>. Microarray analysis revealed a significant number of genes whose expression was commonly affected in the 2 GBM models by orthotopic growth conditions. Consistent with the decrease in sensitivity to foci induction, genes related to reactive oxygen species (ROS) metabolism were expressed at higher levels in the brain tumor xenografts.</p><p><b>Conclusion:</b> γH2AX and 53BP1 foci analyses indicate that GBM cells irradiated within orthotopic xenografts have a greater capacity to repair DSBs and are less susceptible to their induction than tumor cells irradiated under <i>in vitro</i> growth conditions. Because DSB induction and repair are critical determinants of radiosensitivity, these results imply that the brain microenvironment contributes to GBM radioresistance.<i>Clin Cancer Res; 16(24); 6049–59. ©2010 AACR</i>.</p></div>