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作 者:杨泽萱[2] 刘璐[1] 吴清华[1] 朱晓莉[2]
机构地区:[1]东南大学医学院核医学技术研究所,南京210009 [2]东南大学附属中大医院呼吸科
出 处:《中华实验外科杂志》2011年第4期600-602,F0004,共4页Chinese Journal of Experimental Surgery
基 金:基金项目:国家自然科学基金资助项目(30470500)
摘 要:目的探讨白细胞介素-11(IL-11)类似物环九肽c(CGRRAGGSC)与人前列腺癌PC-3细胞的体外结合和在前列腺癌骨转移模型的体内分布。方法印迹蛋白分析PC一-细胞和正常前列腺细胞的IL-11受体(IL-11R)的表达。荧光检测c(CGRRAGGSC)与PC-3细胞的结合位点及内化。将28只荷瘤裸鼠随机分为7组,用99Tcm-标记c(CGRRAGGSC)制备99Tcm-DTPA.c(CGRRAGGSC),经尾静脉注射0.74MBq/0.2ml,观察标记物在荷瘤鼠体内的生物分布。结果PC-3细胞IL-11R是正常前列腺细胞的2.12倍。荧光示踪复染合成物结合在Pc-3细胞膜及胞质。标记物在模型体内迅速持续聚集在瘤体,4h瘤体、骨骼%ID/g达到峰值(15.12±1.19、7.03±1.83),其他脏器分布少,差异有统计学意义(F值依序为71.58、9.58,P〈0.05)。结论环九肽与PC-3细胞的结合具有特异性,标记物能与前列腺癌骨转移灶靶向结合。Objective To assess the specific binding between interleukin-ll (IL-11) analogue c (CGRRAGGSC) and PC-3 cells in vitro and biostribution in bone metastases of prostate cancer in mice in vivo. Methods The expression changes of IL-11R in PC-3 tumors and normal prostate cells were exam- ined by Western blotting. The binding site of the molecular target and internalization with PC-3 cells was observed under a fluorescence microscope. Twenty-eight tumor-bearing nude mice were divided into 7 groups, and radioactive molectdar probe 99Tcm-DT-PA- c (CGRRAG-GSC) was radiolabeled with 99Tcm. Biodistribution in nude mice bearing PC-3 tumors was observed and analyzed after intravenous injection of 99Tcm-DTPA-c (CGRRAGGSC) (0.74 MBq/0.2 ral). Results The expression of IL-11R in PC-3 tumors group was 2. 2 times as the normal group. The counter stain molecular probe was combined with the PC-3 cell membrane and cytoplasm through fluorescence tracing. Uptake of the imaging probe in the tumor was increased. Radioactivity was abnormally concentrated in the tumor lesions and skeleton. Most apparent after 4 h ( 15.12 ± 1.19, 7.03 ± 1.83 ), radiation was not obviously observed in other viscera ( F =71.58, 9. 58 ,P 〈 0. 05). Conclusion c (CGRRAGGSC) peptide has the specific binding ability in targeting to PC-3 cells in vitro. Radioactive molecular probe 99Tcm-DTPA-c (CGRRAGGSC) has potential as a specific molecular target imaging agent for bone metastasis, such as prostate cancer.
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