Veeravagu Anand, Liu Zhaofei, Niu Gang, Chen Kai, Jia Bing, Cai Weibo, Jin Cunjing, Hsu Andrew R, Connolly Andrew J, Tse Victor, Wang Fan, Chen Xiaoyuan
Molecular Imaging Program at Stanford, Department of Radiology and Bio-X Program, Stanford University School of Medicine, Stanford, California 94305-5484, USA.
Clin Cancer Res. 2008 Nov 15;14(22):7330-9. doi: 10.1158/1078-0432.CCR-08-0797.
Abegrin is a monoclonal antibody to human integrin alphavbeta3, a cell adhesion molecule highly expressed on actively angiogenic endothelium and glioblastoma multiforme tumor cells. The purpose of this study was to evaluate the efficacy of a novel 90Y-Abegrin radioimmunotherapeutic agent in murine xenograft glioblastoma models with noninvasive in vivo molecular imaging modalities.
A s.c. U87MG human glioblastoma xenograft model was used to determine maximum tolerated dose (MTD), biodistribution, dose response, and efficacy of 90Y-Abegrin. Antitumor efficacy was also characterized in an orthotopic U87MG and in a HT-29 colorectal cancer model, a low integrin-expressing carcinoma. Small-animal positron emission tomography imaging was used to correlate histologic findings of treatment efficacy.
MTD and dose response analysis revealed 200 microCi per mouse as appropriate treatment dose with hepatic clearance and no organ toxicity. 90Y-Abegrin-treated U87MG tumor mice showed partial regression of tumor volume, with increased tumor volumes in 90Y-IgG, Abegrin, and saline groups. 18F-FDG imaging revealed a reduction of cell proliferation and metabolic activity whereas 18F-FLT reflected decreased DNA synthesis in the 90Y-Abegrin group. Ki67 analysis showed reduced proliferative index and quantitative terminal deoxynucleotidyl transferase dUTP nick-end labeling-positive analysis revealed increased DNA fragmentation and apoptosis in 90Y-Abegrin animals. CD31 and 4',6-diamidino-2-phenylindole staining showed increased vascular fragmentation and dysmorphic vessel structure in 90Y-Abegrin animals only. Orthotopic U87MG tumors treated with 90Y-Abegrin displayed reduced tumor volume. HT-29 tumors showed no significant difference among the various groups.
Radioimmunotherapy with 90Y-labeled Abegrin may prove promising in the treatment of highly vascular, invasive, and heterogeneous malignant brain tumors.
阿贝格林是一种针对人整合素αvβ3的单克隆抗体,整合素αvβ3是一种细胞黏附分子,在活跃的血管生成内皮细胞和多形性胶质母细胞瘤肿瘤细胞上高度表达。本研究的目的是利用无创体内分子成像方式,评估新型90Y-阿贝格林放射免疫治疗剂在小鼠异种移植胶质母细胞瘤模型中的疗效。
采用皮下U87MG人胶质母细胞瘤异种移植模型来确定90Y-阿贝格林的最大耐受剂量(MTD)、生物分布、剂量反应和疗效。还在原位U87MG和HT-29结直肠癌模型(一种整合素表达较低的癌)中对抗肿瘤疗效进行了表征。使用小动物正电子发射断层扫描成像来关联治疗疗效的组织学发现。
MTD和剂量反应分析显示,每只小鼠200微居里为合适的治疗剂量,有肝脏清除且无器官毒性。经90Y-阿贝格林治疗的U87MG肿瘤小鼠的肿瘤体积出现部分消退,而90Y-IgG、阿贝格林和生理盐水组的肿瘤体积增加。18F-FDG成像显示细胞增殖和代谢活性降低,而18F-FLT反映90Y-阿贝格林组的DNA合成减少。Ki67分析显示增殖指数降低,定量末端脱氧核苷酸转移酶dUTP缺口末端标记阳性分析显示90Y-阿贝格林处理的动物中DNA片段化增加且细胞凋亡增加。仅在90Y-阿贝格林处理的动物中,CD31和4',6-二脒基-2-苯基吲哚染色显示血管碎片化增加和血管结构畸形。用90Y-阿贝格林治疗的原位U87MG肿瘤的肿瘤体积减小。HT-29肿瘤在各治疗组之间无显著差异。
用90Y标记的阿贝格林进行放射免疫治疗在治疗高度血管化、侵袭性和异质性恶性脑肿瘤方面可能前景广阔。