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作 者:孙晋[1] 陈道桢[1] 刘璐[2] 邵国强[3] 胡瑶[1] 李天女[1] 谢彦[2] 王强[2] 刘标[1]
机构地区:[1]南京医科大学第一附属医院核医学科,210029 [2]东南大学附属中大医院 [3]南京医科大学
出 处:《中华实验外科杂志》2015年第12期2946-2949,共4页Chinese Journal of Experimental Surgery
基 金:国家自然科学基金资助项目(81202032、81372480、81301247);高等学校博士学科点专项科研基金课题新教师类(20123234120016)
摘 要:目的探讨白细胞介素-11受体(IL-11R)介导的放射性探针对前列腺癌细胞抑制作用。方法构建IL-11R仅亚基靶向的放射性标记探针;免疫荧光评估靶向载体修饰肽对前列腺癌细胞结合能力;细胞计数试剂盒(CCK-8)法、Transwell及划痕法检测放射性标记探针对前列腺癌细胞增殖及迁移抑制作用。结果成功构建131I-Tyr—CGRRAGGSC,放化纯达99%以上;修饰肽与前列腺癌细胞显著结合。1.85、3.70、7.40、1d.80MBq/ml剂量组对PC-3M、DU-145抑制率分别为(9.83±2.55)%、(22.20±2.31)%、(58.87±4.98)%、(65.24±4.99)%和(6.23±3.27)%、(19.48±3.89)%、(32.27±2.87)%、(58.13±4.45)%;Transwell实验示1.85、5.55MBq/ml剂量组迁移率分别为(75.22±6.27)%、(25.58±6.01)%,差异均有统计学意义(P〈0.05)。划痕实验亦证实迁移抑制。结论经IL-11Rα介导的131I—Tyr—CGRRAGGSC对前列腺癌细胞增殖及迁移的抑制作用明确。Corresponding author : Liu Lu , Email : luliuzhou@ sina. corn [ Abstract ] Objective To discuss the inhibitory effects of a interleukin - 11 receptor ( IL - 11R) - mediated radiolabeled probe on prostate cancer. Methods The radiolabeled probe was prepared. Immunoflu- orescence staining was performed to observe the binding status of modified CGRRAGGS. The effects of ra- diolabeled probe were explored on cell proliferation and migration by cell counting kit -8 (CCK -8), Tr- answell and wound - healing assay. Results 1311 - Tyr - CGRRAGGSC was radiolabeled and radiochemical purity after purification was over 99%. The prostate cancer cells had high binding abilities to the modified peptides. Inhibition ratio of 1.85, 3, 70, 7. 40 and 14. 80 MBq/ml ∽3J I - Tyr - CGRRAGGSC was (9. 83 ± 2. 55)%, (22. 20 ±2. 31)%, (38.87 _±4.98)% and (65.24 ±4. 99) % respectively to PC - 3M cells, and (6.23 ±3.27)%, (19.48±3.89)%, (32.27 ±2.87)% and (58. 13 ±4.45)% respectively to DU - 145 cells. The migration ratio of 1.85 MBq/ml and 5.55 MBq/ml groups was (75.22 ±6. 27)% and (25.58±6. 01 )%, respectively, confirmed by wound- healing assay. All the difference was statistically significant (P 〈 0. 05 ). Conclusion Mediated by IL - 1 l receptor, the inhibitory effects of 1311 - Tyr - CGRRAGGSC have been proven on prostate cancer cell proliferation and migration.
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