Salhia Bodour, Rutka James T, Lingwood Clifford, Nutikka Anita, Van Furth Wouter R
Arthur and Sonia Labatt Brain Tumour Research Center, Division of Neurosurgery, The Hospital for Sick Children, The University of Toronto, 555 University Avenue, Toronto, Ontario, Canada M5G 1X8.
Neoplasia. 2002 Jul-Aug;4(4):304-11. doi: 10.1038/sj.neo.7900243.
Malignant meningiomas (MMs) are aggressive intracranial neoplasms with a 75% 5-year recurrence rate. Verotoxin 1 (VT1) is an Escherichia coli toxin, which has recently been shown to have anti-neoplastic action by targeting the globotriosylceramide (Gb(3)) glycolipid on tumor cells and tumor neovasculature. To investigate the potential use of VT1 as a clinical agent for MM, we initially tested 16 meningiomas for Gb(3) expression. Nine of 11 MMs (82%), but only one of five benign meningiomas (20%), were positive for Gb(3). An orthotopic xenograft model was used to test the efficacy of VT1 treatment for MM. We first demonstrated that Gb(3) was highly expressed by the MM cell line, IOMM-Lee, and that this cell line was highly sensitive to VT1 treatment in vitro. A single intratumoral injection of VT1 significantly improved survival in nude mice harboring intracranial tumours (P<.0001). Factor-eight immunostaining of tumours harvested from VT1-treated animals revealed a marked reduction in the tumour microvascular density. In addition, the tumors of VT1-treated animals displayed increased apoptosis by TUNEL analysis and showed a significant decrease in cell proliferation, as determined by MIB-5 immunostaining. VT1 treatment of MM is effective in our orthotopic xenograft model, and warrants further exploration as a potential treatment for these highly anaplastic and aggressive neoplasms.
恶性脑膜瘤(MMs)是侵袭性颅内肿瘤,5年复发率为75%。志贺毒素1(VT1)是一种大肠杆菌毒素,最近研究表明它可通过靶向肿瘤细胞和肿瘤新生血管上的球三糖神经酰胺(Gb(3))糖脂发挥抗肿瘤作用。为了研究VT1作为MM临床治疗药物的潜在用途,我们首先检测了16例脑膜瘤的Gb(3)表达情况。11例MM中有9例(82%)Gb(3)呈阳性,但5例良性脑膜瘤中只有1例(20%)呈阳性。我们使用原位异种移植模型来测试VT1治疗MM的疗效。我们首先证明MM细胞系IOMM-Lee高表达Gb(3),并且该细胞系在体外对VT1治疗高度敏感。单次瘤内注射VT1可显著提高颅内肿瘤裸鼠的生存率(P<0.0001)。对VT1治疗动物所取肿瘤进行的凝血因子VIII免疫染色显示肿瘤微血管密度显著降低。此外,通过TUNEL分析发现,VT1治疗动物的肿瘤细胞凋亡增加,并且通过MIB-5免疫染色确定细胞增殖显著减少。在我们的原位异种移植模型中,VT1治疗MM有效,作为这些高度间变和侵袭性肿瘤的潜在治疗方法值得进一步探索。