大连医科大学学报
大連醫科大學學報
대련의과대학학보
JOURNAL OF DALIAN MEDICAL UNIVERSITY
2015年
2期
109-113
,共5页
罗旭%王聪%范宁%罗文超%徐飞%李岩
囉旭%王聰%範寧%囉文超%徐飛%李巖
라욱%왕총%범저%라문초%서비%리암
肺鳞癌%肺腺癌%S100A4%siRNA
肺鱗癌%肺腺癌%S100A4%siRNA
폐린암%폐선암%S100A4%siRNA
squamous carcinoma%adenocarcinoma%S100A4%siRNA
目的:研究S100A4在肺鳞癌与肺腺癌细胞系中的表达及对细胞增殖、转移、侵袭功能的影响。方法利用RT-PCR和Western Blot检测S100A4在肺鳞癌细胞系NCI-H520和肺腺癌细胞系SPC-A-1中的表达,利用siRNA干扰S100A4在两个细胞系的表达,CCK-8检测细胞增殖,划痕、Transwell实验检测细胞迁移侵袭。结果 RT-PCR与Western Blot检测结果显示S100A4在肺鳞癌及肺腺癌细胞系中均有表达,且肺鳞癌细胞系NCI-H520中S100A4表达水平低于肺腺癌细胞系SPC-A-1(P<0.05)。细胞荧光、Western Blot 及RT-PCR验证S100A4敲除效率,CCK-8实验证明干扰S100A4后,两肺癌细胞系的增殖能力较空白对照组和阴性对照组均降低(P<0.05)、划痕及Tranwell实验证明干扰S100A4后,两肺癌细胞系的迁移能力与对照组相比也降低(P<0.05)。结论 S100A4在肺鳞癌细胞系与肺腺癌细胞系均有表达,且鳞癌高于腺癌,S100A4与肺癌细胞恶性进展有关,有可能成为肺癌治疗的新靶点。
目的:研究S100A4在肺鱗癌與肺腺癌細胞繫中的錶達及對細胞增殖、轉移、侵襲功能的影響。方法利用RT-PCR和Western Blot檢測S100A4在肺鱗癌細胞繫NCI-H520和肺腺癌細胞繫SPC-A-1中的錶達,利用siRNA榦擾S100A4在兩箇細胞繫的錶達,CCK-8檢測細胞增殖,劃痕、Transwell實驗檢測細胞遷移侵襲。結果 RT-PCR與Western Blot檢測結果顯示S100A4在肺鱗癌及肺腺癌細胞繫中均有錶達,且肺鱗癌細胞繫NCI-H520中S100A4錶達水平低于肺腺癌細胞繫SPC-A-1(P<0.05)。細胞熒光、Western Blot 及RT-PCR驗證S100A4敲除效率,CCK-8實驗證明榦擾S100A4後,兩肺癌細胞繫的增殖能力較空白對照組和陰性對照組均降低(P<0.05)、劃痕及Tranwell實驗證明榦擾S100A4後,兩肺癌細胞繫的遷移能力與對照組相比也降低(P<0.05)。結論 S100A4在肺鱗癌細胞繫與肺腺癌細胞繫均有錶達,且鱗癌高于腺癌,S100A4與肺癌細胞噁性進展有關,有可能成為肺癌治療的新靶點。
목적:연구S100A4재폐린암여폐선암세포계중적표체급대세포증식、전이、침습공능적영향。방법이용RT-PCR화Western Blot검측S100A4재폐린암세포계NCI-H520화폐선암세포계SPC-A-1중적표체,이용siRNA간우S100A4재량개세포계적표체,CCK-8검측세포증식,화흔、Transwell실험검측세포천이침습。결과 RT-PCR여Western Blot검측결과현시S100A4재폐린암급폐선암세포계중균유표체,차폐린암세포계NCI-H520중S100A4표체수평저우폐선암세포계SPC-A-1(P<0.05)。세포형광、Western Blot 급RT-PCR험증S100A4고제효솔,CCK-8실험증명간우S100A4후,량폐암세포계적증식능력교공백대조조화음성대조조균강저(P<0.05)、화흔급Tranwell실험증명간우S100A4후,량폐암세포계적천이능력여대조조상비야강저(P<0.05)。결론 S100A4재폐린암세포계여폐선암세포계균유표체,차린암고우선암,S100A4여폐암세포악성진전유관,유가능성위폐암치료적신파점。
Objective To explore the expression of S100A4 in lung squamous carcinoma and adenocarcinoma cells and its effection in proliferation,metastasis,invasion.Meth ods RT-PCR and Western Blot were used to detect the expression of S100A4 in lung squamous carcinoma NCI-H520 and adenocarcinoma SPC-A-1 cell lines,using siRNA to knockdown S100A4 in these two cell lines and CCK-8,wound healing assay and transwell experiment were used to detect the cell pro-liferation,migration and invasion.Results The expression of S100A4 was different in these two cell lines and the expression was lower in squamous carcinoma than adenocarcinoma (P<0.05).The transfection efficiency was detected by immuno-fluorescence,Western Blot and RT-PCR.Knocking down S100A4 significantly reduced the cell proliferation,migration which was confirmed by CCK-8,wound healing and transwell assay (P<0.05).Conclusion Expression of S100A4 in lung squamous carcinoma NCI-H520 was significantly lower than adenocarcinoma SPC-A-1 cell line.Knocking down S100A4 reduced the lung cancer cell malignant and may be a potential target for lung cancer treatment.