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作 者:宋佳佳[1] 卢永宁[1] 张进[1] 黄翼然[1]
机构地区:[1]上海交通大学医学院附属仁济医院泌尿外科,200127
出 处:《中华医学杂志》2014年第34期2704-2707,共4页National Medical Journal of China
基 金:国家自然科学基金(81272841);上海市自然科学基金(13ZR1425100);上海市卫生计生委课题(2013SY027)志谢感谢中国科学院上海药物所提供技术支持
摘 要:目的 观察肾癌细胞株786-O、Caki-1与正常人肾成纤维细胞(NHRF)相互作用后,肾癌细胞对依维莫司敏感性的变化.方法 建立肾癌细胞与成纤维细胞共培养体系,观察共培养后786-O、Caki-1的增殖及迁移能力[用吸光度(A)值表示]变化以及肾癌细胞对依维莫司敏感性的改变.结果 共培养后,786-O组肾癌细胞细胞增殖能力较对照组A值显著增加22%(2.35±0.05与1.93±0.15,P=0.01),Caki-1组A值较对照组显著增加约80%(2.35±0.21与1.24±0.11,P=0.001);迁移能力有所增强:786-O A值较对照组显著增加(1.34±0.12与0.86±0.04,P=0.03),Caki-1 A值较对照组显著增加(1.53 ±0.11与0.98 ±0.11,P=0.04).此外共培养组经依维莫司(1、5、10 μmol/L)处理后,在1μmol/L时,786-O组和对照组相比抑制率降低(24.05±5.05)%与(12.45±2.44)%,P=0.04,在5、10 μmol/L时抑制率无明显变化(P值分别为0.35、0.18);Caki-1共培养组和对照组相比,抑制率均明显降低(49.02±2.17)%与(4.96±0.50)%,P=0.02;(52.67±2.57)%与(12.36±0.29)%,P=0.03;(60.87±3.87)%与(35.10±2.45)%,P=0.024.结论 NHRF促进肾癌细胞株786-O、Caki-1的增殖及迁移;NHRF参与786-O、Caki-1对依维莫司耐药现象的发生.Objective To observe the effects of normal human renal fibroblast (NHRF) on renal cell carcinoma cell lines.Methods Renal cell carcinoma (RCC) cell lines 786-O and Caki-1 were cocultured with NHRF for assessing the proliferation and migratory capacities of renal cell carcinoma cell lines and the sensitivity to everolimus.Results Co-culturing with NHRF substantially increased the proliferation capacity of both RCC cell lines (786-O:2.35 ± 0.05 vs1.93 ± 0.15,P =0.01 ; Caki-1:2.35 ± 0.21 vs 1.24 ± 0.11,P =0.001).Similarly the migratory capacities of both cell lines became significantly enhanced after co-culturing (786-O:1.53 ± 0.11 vs 0.98 ± 0.11,P =0.04 ; Caki-1:1.53 ± 0.11 vs 0.98 ± 0.11,P =0.04) compared with untreated control.Furthermore,the sensitivities of both cell lines to everolimus (1,5,10 μmol/L) dramatically decreased in those pre-co-cultured with NHRF (786-O:P value 0.04,0.35,0.18) ; Caki-1:P value 0.02,0.03,0.024).Conclusion NHRF promotes the proliferation and migration capacities of 786-O and Caki-1.And it may be involved in the resistance of RCC to everolimus.
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