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作 者:陈维真[1] 张勇[1] 卢汉平[2] 梁昌盛[3] 谢瑶[4] 刘长征[2]
机构地区:[1]中山大学附属第三医院核医学科,广东广州510630 [2]中山大学基础医学院实验核医学教研室,广东广州510080 [3]中山大学基础医学实验教学中心,广东广州510080 [4]中山大学基础医学院人体解剖学教研室,广东广州510080
出 处:《中国病理生理杂志》2007年第10期2051-2053,共3页Chinese Journal of Pathophysiology
基 金:广东省科技计划资助项目(No.2003B30103)
摘 要:目的:探讨铼-188(188Re)标记前列腺特异膜抗原单克隆抗体7E11C5.3(188Re-7E11C5.3)对前列腺癌细胞系LNCaP的体外抑制作用。方法:采用2-巯基乙醇直接还原法制备188Re-7E11C5.3标记物,纸层析法测定标记率和放化纯度,直线回归外推法测定免疫活性分数。四唑盐(MTT)法测定其体外细胞毒作用。结果:188Re-7E11C5.3的标记率为(93.16±2.18)%,放化纯度为(95.62±0.48)%,免疫活性分数为(74.86±1.86)%。188Re-7E11C5.3对LNCaP细胞的生长抑制作用明显强于188Re标记的正常鼠IgG(mIgG)和游离188ReO4-,其半数有效抑制浓度(IC50)分别为(23.38±3.73)×107Bq/L,(59.21±8.02)×107Bq/L和(68.89±10.91)×107Bq/L。结论:188Re-7E11C5.3能有效抑制体外培养LNCaP细胞的增殖,可用于前列腺癌的放射免疫治疗。AIM: To investigate the effect of 188 Re labeled monoclonal antibody on prostatic specific membrane antigen 7E1 1 C5.3, radioimmunotherapy for the treatment of human prostate cancer cell line LNCaP in vitro. METHODS : 188 Re -7E1 1 C5.3 was prepared by direct 2 - mercaptoethanol reduction method. Labeling efficiency and radiochemical purity was measured by paper chromatography. Immunoreactive fraction was determined by linear extrapolation. Cytotoxicity to LNCaP cells was determined by MTT assay. RESULTS: The labeling yield of 188 Re -7E1 1 C5.3 was (93. 16 ±2. 18 )% , the radiochemical purity was (95.62 ±0. 48)% , and the immunoreactive fraction was (74. 86± 1.86)%. The inhibitory effect of 188Re -7E11C5.3 on cell proliferation of LNCaP cells was significantly higher than that of 188Re - mlgG or 188 ReO4^-. The 50% inhibitory doses ( IC50 ) of 188Re - 7E1 1 C5.3, 188 Re - mIgG, and lss ReO4^- were (23.38 ±3.73 ) ×10^7 Bq/L, (59. 21 ±8.02) × 10^7 Bq/L and (68.89 ±10. 91 ) × 10^7 Bq/L, respectively. CONCLUSION: 188Re - 7E11C5.3 can effectively inhibit the growth of in vitro cultured prostate cancer cells and shows much potential for prostate cancer radioimmunotherapy.
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