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作 者:陈维真[1] 张勇[1] 梁昌盛[2] 谢瑶[3] 温新桥[4] 高新[4]
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教学中心,广东广州510080 [3]中山大学基础医学院人体解剖学教研室,广东广州510080 [4]中山大学附属第三医院泌尿外科,广东广州510630
出 处:《南方医科大学学报》2008年第3期406-408,共3页Journal of Southern Medical University
基 金:广东省科技计划项目(2003B30103)~~
摘 要:目的探讨导向化疗对前列腺癌细胞系LNCaP的体外作用。方法以葡聚糖为中介体制备抗前列腺癌单克隆抗体7E11C5.3与平阳霉素(PYM)的偶联物,用间接ELISA法测定其免疫活性,2,3,5-氯化三苯基四氮唑法测定其抑菌活性,四唑盐法测定其体外细胞毒作用。结果偶联物中7E11C5.3和PYM的摩尔比为1:54,偶联后单抗的免疫活性降低了10% ̄20%,偶联物中PYM的抑菌活性为游离PYM的25%,偶联物和游离PYM对体外培养的LNCaP细胞50%抑制浓度分别为(9.41±1.98)μg/ml和(29.92±7.88)μg/ml。结论7E11C5.3-PYM偶联物的体外抗前列腺癌作用强于游离PYM。Objective To investigate the effect of antibody-targeted chemotherapy against human prostate cancer LNCaP cells in vitro. Methods The monoclonal antibody 7E11C5.3 against human prostate cancer was conjugated to pingyangrnycin (PYM), mediated by dextran T-40, and the immunoreactivity of 7E11C5.3 was determined by indirect enzyme-linked irnmunosorbent assay. The bacteriostatic activity of the conjugate was determined using TTC assay, and its cytotoxicity against LNCaP cells was determined by MTT assay. Results The 7El IC5.3:PYM molar ratio was 1:54 in the conjugate, and the immunoreactivity of 7E11C5.3 was decreased by approximately 10% to 20% after conjugation. The bacteriostatic activity of conjugated PYM was 25% of that of free PYM. The 50% inhibitory doses (IC50) of7E11C5.3-PYM conjugate and free PYM against the in vitro cultured LNCaP cells were 9.41±1.98 p,g/ml and 29.92±7.88 μg/ml, respectively. Conclusion 7El IC5.3-PYM conjugate displays stronger cytotoxicity against anti-prostate cancer effects than rice PYM.
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