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首页> 外文期刊>European journal of gynaecological oncology >The effect of RNAi silencing Tspan5 expression on the proliferation and migration of human choriocarcinoma cell line JEG-3
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The effect of RNAi silencing Tspan5 expression on the proliferation and migration of human choriocarcinoma cell line JEG-3

机译:RNAI沉默的TSPAN5表达对人核心癌细胞系jeg-3的增殖和迁移的影响

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摘要

Objective: To study the effect of Tspan5 on the proliferation and migration of trophoblast cell, seeking a new target for the treatment of gestational trophoblastic disease. Materials and Methods: The authors used RNAi to silence the Tspan5 expression in human choriocarcinoma cell line JEG-3 first, and then used Western blotting to detect the expression of Tspan5, calculating the efficiency of interference. CCK-8 test, colony formation, and scratch assay were used to detect the proliferation and migration of the before and after interference JEG-3 cells. Results: Western blotting results showed that Tspan5/NC band gray value was highest and Tspan5/1005 lowest, so the authors chose Tspan5/1005 as an interference group to finish the follow-up experiment. Interference group (Tspan5/1005) clone number of JEG-3 cell was significantly reduced compared with the control group (Tspan5/NC) (148 +/- 23 vs. 276 +/- 31, p 0.01). There was no significant difference between blank group and control group (328 +/- 39 vs. 276 +/- 31, p 0.1). The JEG-3 cell proliferation activity of blank group was the highest, the control group (Tspan5/NC) group's proliferation activity was slightly lower, however there was no significant difference (1.200 +/- 0.103 vs. 1.185 +/- 0.022, p 0.05) between the two. Compared with the control group (Tspan5/NC), the JEG-3 cell proliferation activity of interference group (Tspan5/1005) decreased significantly (1.185 +/- 0.022 vs. 1.076 +/- 0.028, p 0.01). In the absolute value of the scratch width, 24 hours after scratching minus the scratch width 0 hours after scratching, the interference group (Tspan5/1005) was significantly less than the control group (Tspan5/NC) (1.27 +/- 0.03 cm vs. 1.97 +/- 0.38 cm, p 0.05). Conclusion: In this study, the authors found that the proliferation and migration of choriocarcinoma cells were reduced after using RNAi technology to knockdown Tspan5 expression. The quantity of Tspan5 expression was positively related with proliferation and migration of choriocarcinoma cells.
机译:目的:研究TSPAN5对滋养细胞增殖和迁移的影响,寻求妊娠期孕产病治疗的新靶。材料和方法:作者使用RNAi将TSPAN5表达沉默于人核心癌细胞系jeg-3中,然后使用蛋白质印迹来检测TSPAN5的表达,计算干扰效率。 CCK-8测试,菌落形成和划痕测定用于检测干扰JEG-3细胞前后的增殖和迁移。结果:Western印迹结果表明,TSPAN5 / NC带灰度值最高,TSPAN5 / 1005最低,因此作者将TSPAN5 / 1005选择为干扰组,以完成后续实验。与对照组(TSPAN5 / NC)相比,干扰组(TSPAN5 / 1005)JEG-3细胞的克隆数目明显减少(148 +/- 23 vs.276 +/- 31,P& 0.01)。空白组和对照组之间没有显着差异(328 +/- 39与276 +/- 31,P& 0.1)。空白组的JEG-3细胞增殖活性最高,对照组(TSPAN5 / NC)组的增殖活性略低,但没有显着差异(1.200 +/- 0.103,比1.185 +/- 0.022,p & 0.05)两者之间。与对照组(TSPAN5 / NC)相比,干扰组的JEG-3细胞增殖活性(TSPAN5 / 1005)显着降低(1.185 +/- 0.022,1.076 +/- 0.028,P <0.01)。在划痕宽度的绝对值中,刮伤后24小时减去划痕宽度0小时后,干扰组(TSPAN5 / 1005)明显小于对照组(TSPAN5 / NC)(1.27 +/- 0.03 cm Vs 。1.97 +/- 0.38厘米,P <0.05)。结论:在本研究中,作者发现,使用RNAI技术敲低TSPAN5表达后,减少了刺槐癌细胞的增殖和迁移。 TSPAN5表达的量与甘露曲集产瘤细胞的增殖和迁移呈正相关。

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