Departments of Cancer Biology and Genetics, Brain Tumor Center, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Cancer Res. 2010 Mar 15;70(6):2548-57. doi: 10.1158/0008-5472.CAN-09-2503. Epub 2010 Mar 2.
Brainstem gliomas (BSG) are a rare group of central nervous system tumors that arise mostly in children and usually portend a particularly poor prognosis. We report the development of a genetically engineered mouse model of BSG using the RCAS/tv-a system and its implementation in preclinical trials. Using immunohistochemistry, we found that platelet-derived growth factor (PDGF) receptor alpha is overexpressed in 67% of pediatric BSGs. Based on this observation, we induced low-grade BSGs by overexpressing PDGF-B in the posterior fossa of neonatal nestin tv-a mice. To generate high-grade BSGs, we overexpressed PDGF-B in combination with Ink4a-ARF loss, given that this locus is commonly lost in high-grade pediatric BSGs. We show that the likely cells of origin for these mouse BSGs exist on the floor of the fourth ventricle and cerebral aqueduct. Irradiation of these high-grade BSGs shows that although single doses of 2, 6, and 10 Gy significantly increased the percent of terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL)-positive nuclei, only 6 and 10 Gy significantly induce cell cycle arrest. Perifosine, an inhibitor of AKT signaling, significantly induced TUNEL-positive nuclei in this high-grade BSG model, but in combination with 10 Gy, it did not significantly increase the percent of TUNEL-positive nuclei relative to 10 Gy alone at 6, 24, and 72 hours. Survival analysis showed that a single dose of 10 Gy significantly prolonged survival by 27% (P = 0.0002) but perifosine did not (P = 0.92). Perifosine + 10 Gy did not result in a significantly increased survival relative to 10 Gy alone (P = 0.23). This PDGF-induced BSG model can serve as a preclinical tool for the testing of novel agents.
脑干神经胶质瘤(BSG)是一组罕见的中枢神经系统肿瘤,主要发生在儿童中,通常预示着预后特别差。我们报告了使用 RCAS/tv-a 系统开发 BSG 的基因工程小鼠模型及其在临床前试验中的应用。通过免疫组织化学,我们发现血小板衍生生长因子(PDGF)受体α在 67%的小儿 BSG 中过表达。基于这一观察结果,我们通过在神经巢蛋白 tv-a 新生鼠的后颅窝过表达 PDGF-B 来诱导低级别 BSG。为了生成高级别 BSG,我们过表达 PDGF-B 并结合 Ink4a-ARF 缺失,因为该基因座在高级别小儿 BSG 中经常丢失。我们表明,这些小鼠 BSG 的可能起源细胞存在于第四脑室和脑导水管的底部。对这些高级别 BSG 进行照射表明,尽管单次给予 2、6 和 10 Gy 剂量显著增加了末端脱氧核苷酸转移酶介导的 dUTP 缺口末端标记(TUNEL)阳性核的百分比,但只有 6 和 10 Gy 显著诱导细胞周期停滞。Perifosine 是一种 AKT 信号抑制剂,可显著诱导该高级别 BSG 模型中的 TUNEL 阳性核,但与 10 Gy 联合使用时,与单独给予 10 Gy 相比,在 6、24 和 72 小时时,TUNEL 阳性核的百分比并未显著增加。生存分析表明,单次给予 10 Gy 剂量可使生存时间延长 27%(P=0.0002),但 perifosine 无此作用(P=0.92)。Perifosine + 10 Gy 与单独给予 10 Gy 相比,并未导致生存时间显著延长(P=0.23)。这种由 PDGF 诱导的 BSG 模型可以作为测试新型药物的临床前工具。