^131I标记抗VEGFR2靶向性纳米载体对未分化甲状腺癌的抑瘤作用  被引量:5

Targeted Molecular Diagnosis and Therapy Antitumor effect of ^131I-labeled anti-VEGFR2 targeted nanoparticles in anaplastic thyroid carcinoma mouse models

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作  者:王任飞[1] 张瑞国[1] 张月倩 谌红彬 李宁[1] 张富海[1] 王汉杰 常津 张桂芝[1] 谭建[1] Wang Renfei;Zhang Ruiguo;Zhang Yueqian;Chen Hongbin;Li Ning;Zhang Fuhai;Wang Hanjie;Chang Jin;Zhang Guizhi;Tan Jian(Department of Nuclear Medicine,Tianjin Medical University General Hospital,Tianjin 300052,Chin;School of Life Sciences,Tianjin University,Tianjin 300072,China)

机构地区:[1]天津医科大学总医院核医学科,300052 [2]天津大学生命科学学院,300072

出  处:《中华核医学与分子影像杂志》2018年第11期716-720,共5页Chinese Journal of Nuclear Medicine and Molecular Imaging

摘  要:目的观察131I-牛血清白蛋白(BSA)-介孔二氧化硅纳米粒(MSNs)-抗血管内皮生长因子受体2(anti-VEGFR2)在未分化甲状腺癌(ATC)荷瘤裸鼠体内的靶向性分布及其抑瘤作用。方法构建131I-BSA-MSNs-anti-VEGFR2与131I-BSA-MSNs。分别于人ATC细胞FRO荷瘤裸鼠瘤体内注射131I-BSA-MSNs-anti-VEGFR2(靶向组)、131I-BSA-MSNs(非靶向组)、Na131I(Na131I组)和生理盐水(对照组),通过SPECT/CT显像观察注射后不同时间荷瘤裸鼠体内的放射性分布,记录各组荷瘤裸鼠的体质量及肿瘤体积变化。采用两样本t检验和log-rank法分析数据。结果温育3 h后,靶向组细胞荧光强度(345.26±16.35)高于非靶向组(280.61±9.65;t=5.90,P〈0.05)。SPECT/CT显像示,注射后1~3周,靶向组肿瘤内放射性分布明显强于非靶向组(t值:7.060~12.780,均P〈0.05)。观察结束时,Na131I组、对照组、非靶向组、靶向组的肿瘤体积分别增大至原来的(278.3±19.3)%、(296.6±24.2)%、(198.7±13.2)%和(103.7±6.2)%;前2组裸鼠体质量分别减少为原来的(88.6±3.0)%和(86.2±3.1)%,而后2组则增加至原来的(102.1±3.1)%和(116.2±3.4)%。生存分析曲线显示,靶向组的生存期(38 d)明显高于非靶向组(34 d; χ2=8.05,P〈0.05)。结论131I-BSA-MSNs-anti-VEGFR2可有效抑制ATC的肿瘤生长,延长荷瘤裸鼠生存期,在ATC的治疗和预后评估中有良好的应用前景。ObjectiveTo investigate the radioactivity distribution of 131I-bovine serum albumin (BSA)-mesoporous silica nanoparticles (MSNs)-anti-vascular endothelial growth factor receptor 2 (VEGFR2) in anaplastic thyroid carcinoma (ATC) and to explore its antitumor efficacy in ATC-bearing nude mouse models.Methods131I-BSA-MSNs-anti-VEGFR2 and 131I-BSA-MSNs were constructed. FRO tumor xenografts were established and the SPECT/CT images of tumor-bearing mice were acquired at different time points after intratumoral injection with 131I-BSA-MSNs-anti-VEGFR2 (targeting group), 131I-BSA-MSNs (non-targeting group), Na131I (Na131I group) and saline (control group), respectively. The changes of body mass and tumor volume in each group were recorded. Two-sample t test and log-rank test were used to analyze the data.ResultsAfter incubation for 3 h, the fluorescence intensity in targeting group was higher than that in non-targeting group (345.26±16.35 vs 280.61±9.65; t=5.90, P〈0.05). After injection for 1-3 weeks, the radioactivity detected by SPECT/CT in targeting group was obviously stronger than that in non-targeting group (t values: 7.060-12.780, all P〈0.05). At the end of the observation, the tumor volume of Na131I group, control group, non-targeting group and targeting group increased to (278.3±19.3)%, (296.6±24.2)%, (198.7±13.2)% and (103.7±6.2)% of the original volume, respectively. The body mass of the first 2 groups decreased to (88.6±3.0)% and (86.2±3.1)% of the original body mass respectively, while that of the latter 2 groups increased to (102.1±3.1)% and (116.2±3.4)% of the original body mass respectively. Survival analysis showed that the median survival time in targeting group (38 d) was significantly longer than that in non-targeting group (34 d; χ2=8.05, P〈0.05).Conclusion131I-BSA-MSNs-anti-VEGFR2 can effectively inhibit the tumor growth of ATC and prolong the survival of tumor-bearing nude mice, which gives a good sugg

关 键 词:甲状腺肿瘤 血管内皮生长因子受体2 纳米粒 碘放射性同位素 体层摄影术 发射型计算机  单光子 体层摄影术 X线计算机 小鼠   

分 类 号:R736.1[医药卫生—肿瘤]

 

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