Radiation Oncology Branch, National Cancer Institute, Bethesda, Maryland.
Radiation Oncology Branch, National Cancer Institute, Bethesda, Maryland; Department of Clinical Neurosciences, University of Cambridge, Cambridge, United Kingdom; Wake Forest University School of Medicine, Winston-Salem, North Carolina.
Int J Radiat Oncol Biol Phys. 2020 May 1;107(1):194-201. doi: 10.1016/j.ijrobp.2020.01.007. Epub 2020 Jan 25.
The various microenvironments that exist within the brain combined with the invasive nature of glioblastoma (GBM) creates the potential for a topographic influence on tumor cell radiosensitivity. The aim of this study was to determine whether specific brain microenvironments differentially influence tumor cell radioresponse.
GBM stem-like cells were implanted into the right striatum of nude mice. To measure radiosensitivity, proliferation status of individual tumor cells was determined according to the incorporation of 5-chloro-2'-deoxyuridine delivered at 4, 12, and 20 days after brain irradiation. As an additional measure of radiosensitivity, the percentage of human cells in the right hemisphere and the olfactory bulb were defined using digital droplet polymerase chain reaction. Targeted gene expression profiling was accomplished using NanoString analysis.
Tumor cells were detected throughout the striatum, corpus callosum, and olfactory bulb. After an initial loss of proliferating tumor cells in the corpus callosum and striatum after irradiation, there was only a minor recovery by 20 days. In contrast, the proliferation of tumor cells located in the olfactory bulb began to recover at 4 days and returned to unirradiated levels by day 12 postirradiation. The percentage of human cells in the right hemisphere and the olfactory bulb after irradiation also suggested that the tumor cells in the olfactory bulb were relatively radioresistant. Gene expression profiling identified consistent differences between tumor cells residing in the olfactory bulb and those in the right hemisphere.
These results suggest that the olfactory bulb provides a radioresistant niche for GBM cells.
大脑内部存在的各种微环境与胶质母细胞瘤(GBM)的侵袭性相结合,为肿瘤细胞放射敏感性的地形影响创造了潜力。本研究旨在确定特定的脑微环境是否会对肿瘤细胞的放射反应产生差异影响。
将 GBM 干细胞样细胞植入裸鼠右侧纹状体。为了测量放射敏感性,根据脑照射后 4、12 和 20 天内 5-氯-2'-脱氧尿苷的掺入,确定单个肿瘤细胞的增殖状态。作为放射敏感性的附加测量指标,使用数字液滴聚合酶链反应定义右侧大脑半球和嗅球中人类细胞的百分比。使用 NanoString 分析完成靶向基因表达谱分析。
肿瘤细胞在纹状体、胼胝体和嗅球中均有检测到。照射后胼胝体和纹状体中的增殖性肿瘤细胞最初丢失后,到 20 天仅略有恢复。相比之下,位于嗅球中的肿瘤细胞的增殖在 4 天开始恢复,到照射后 12 天恢复到未照射水平。照射后右侧大脑半球和嗅球中人类细胞的百分比也表明嗅球中的肿瘤细胞相对抗辐射。基因表达谱分析确定了位于嗅球中的肿瘤细胞与位于右侧大脑半球的肿瘤细胞之间存在一致的差异。
这些结果表明,嗅球为 GBM 细胞提供了一个放射抗性小生境。