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作 者:陈葳[2] 赵乐[2] 刘婷[2] 李旭[2] 张丽瑞[1]
机构地区:[1]西安交通大学医学院第一附属医院妇产科,710061 [2]西安交通大学医学院第一附属医院医学转化中心,710061
出 处:《中华实验外科杂志》2013年第8期1683-1685,共3页Chinese Journal of Experimental Surgery
基 金:国家自然科学基金资助项目(30973429、81202055)
摘 要:目的观察肿瘤坏死因子-α(TNF-α)诱导人膀胱癌细胞的上皮间质转化(EMT)及分子机制。方法5μg/LTNF-α处理BLX细胞,凝胶迁移实验(EMSA)观察NF-κB活性,Westernblot和免疫荧光检测波形蛋白(Vimentin)和E-钙黏蛋白(E-cadherin)的表达及定位,体外侵袭转移实验观察细胞侵袭转移能力。逆转录-聚合酶链反应(RT-PCR)检测EMT相关转录因子的表达。结果TNF-α激活核转录因子-κB(NF-κB),促使细胞由多边形向纺锤形转换,E-cadherin表达下调(0.37±0.08比0.75±0.15,P〈0.05)且细胞膜定位消失,Vimentin表达上调(0.46±0.12比0.00±0.00,P〈0.05),细胞转移和侵袭能力提高(182.00±17.58比134.00±9.00;119.00±7.21比85.33±10.11,P〈0.05)。TNF-α诱导Twist和Slug转录因子表达上调(0.91±0.03比0.36±0.07;0.78±0.11比0.22±0.10,P〈0.01)。结论TNF-α激活NF-κB诱导膀胱癌细胞发生EMT,可能在膀胱癌侵袭转移中发挥作用。Objective To investigate the effects of nuclear factor-kappaB (NF-κB) activity in- duced by tumor necrosis factor-α (TNF-α) on epithelial-mesenchymal transition (EMT) of bladder cancer cells. Methods BLX cells were treated with TNF-α (5 μg/L) and the morphological changes were exam- ined by phase contrast microscope. NF-κB activiy of BLX cells was measured by electrophoretic mobility shift assay (EMSA). Vimentin and E-cadherin were detected by using Western blotting and immunofluo- rescent assay. In vitro migration and invasion abilities were determined by using Millice11 assay. EMT-relat- ed molecules were examined by using reverse transcription-polytnerase chain reaction (RT-PCR). Results TNF-α could induce NF-κB activity in BLX cells, promoting the converstion of BLX cells from rounded ep- ithelial-like cells to fibroblast-like cells with elongated morphologies. The BLX cells treated with TNF-αshowed the downregulation of E-cadherin protein ( 0. 37 ± 0. 08 vs. 0. 75 ± 0. 15, P 〈 0. 05 ), especially membrane localization loss, and upregulation of vimentin protein ( 0. 46 ± 0. 12 vs. 0. 00 ± 0. 00, P 〈 0. 05). TNFα-treated BLX cells showed more motile and invasive than untreated control cells (182. 00 ± 17.58 vs. 134. 00 ± 9. 00 ; 119.00 ± 7.21 vs. 85.33 ± 10. 11, P 〈 0. 05). Moreover, the upregulation of Twist and Slug was demonstrated in TNFα-treated BLX ceils compared to control cells (0. 91 ± 0. 03 vs. 0. 36 ± 0. 07 ; 0. 78 ± 0. 11 vs. 0. 22 ± 0. 10, P 〈 0.01 ). Conclusion Activation of NF-κB induced by TNF-α promotes EMT in bladder cancer cells, suggesting that NF-κB may also be a potential target for sup- pressing the metastasis and invasion of the bladder carcinoma.
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