机构地区:[1]江汉大学医学院病理学与病理生理学教研室,武汉430056
出 处:《国际肿瘤学杂志》2018年第1期1-4,共4页Journal of International Oncology
摘 要:目的研究敲低信号转导子和转录激活子5(Stat5)对甲状腺癌TT细胞侵袭及上皮间质转化(EMT)的影响。方法培养甲状腺癌TT细胞并分为Stat5小干扰RNA(siRNA)组和NCsiRNA组,分别转染Stat5的siRNA和阴性对照的NCsiRNA。转染后,采用Transwell模型检测细胞的侵袭数目,采用荧光定量PCR试剂盒测定细胞中基质金属蛋白酶(MMP)家族基因、EMT标志基因、血管新生基因的表达量。结果转染siRNA后12 h、18 h、24 h,Stat5siRNA组细胞的侵袭数目均显著低于NCsiRNA组(42.39±5.82∶64.41±8.49,t=-4.784,P=0.001;51.23±6.38∶78.54±9.52,t=-5.329,P<0.001;60.35±8.35∶98.42±11.25,t=-6.076,P<0.001)。转染siRNA后24 h,Stat5siRNA组细胞中MMP1、MMP2、MMP9、MMP13、神经型钙黏蛋白(Ncadherin)、波形蛋白(Vimentin)、血管内皮生长因子(VEGF)、碱性纤维母细胞生长因子(bFGF)、血管生成素(Ang)1、Ang2的mRNA表达量均显著低于NCsiRNA组(0.42±0.07∶1.03±0.15,t=-8.240,P<0.001;0.35±0.06∶1.01±0.13,t=-10.307,P<0.001;0.29±0.05∶1.05±0.18,t=-9.097,P<0.001;0.54±0.08∶0.98±0.12,t=-6.822,P<0.001;0.38±0.06∶1.04±0.18,t=-7.778,P<0.001;0.29±0.04∶1.06±0.12,t=-12.612,P<0.001;0.36±0.07∶1.06±0.14,t=-10.000,P<0.001;0.43±0.08∶0.97±0.12,t=-8.372,P<0.001;0.25±0.03∶1.03±0.12,t=-14.100,P<0.001;0.19±0.03∶0.99±0.13,t=-13.408,P<0.001),上皮细胞钙黏蛋白(Ecadherin)的mRNA表达量显著高于NCsiRNA组(2.88±0.42∶0.98±0.12,t=9.726,P<0.001)。结论敲低Stat5对甲状腺癌TT细胞侵袭及EMT具有抑制作用。ObjectiveTo investigate the effects of knockdown of signal transducer and activator of transcription 5 (Stat5) on invasion and epithelial mesenchymal transition (EMT) of thyroid carcinoma TT cells. MethodsThyroid carcinoma TT cells were cultured and divided into Stat5small interfering RNA (siRNA) group and NCsiRNA group, transfected with Stat5 siRNA and negative control NCsiRNA respectively. After transfection, the numbers of invasive cells were determined by Transwell model and the expressions of matrix metalloproteinase (MMP) family genes, EMT marker genes, angiogenesis genes in the cells were determined by fluorescent quantitative PCR. ResultsThe numbers of invasive cells in Stat5siRNA group were significantly lower than those in NCsiRNA group (42.39±5.82 vs. 64.41±8.49, t=-4.784, P=0.001; 51.23±6.38 vs. 78.54±9.52, t=-5.329, P〈0.001; 60.35±8.35 vs. 98.42±11.25, t=-6.076, P〈0.001) after the transfection of siRNA for 12 hours, 18 hours and 24 hours. Twentyfour hours after transfection of siRNA, the mRNA expressions of MMP1, MMP2, MMP9, MMP13, Ncadherin, Vimentin, vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), angiogenin (Ang)1 and Ang2 in Stat5siRNA group were significantly lower than those in NCsiRNA group (0.42±0.07 vs. 1.03±0.15, t=-8.240, P〈0.001; 0.35±0.06 vs. 1.01±0.13, t=-10.307, P〈0.001; 0.29±0.05 vs. 1.05±0.18, t=-9.097, P〈0.001; 0.54±0.08 vs. 0.98±0.12, t=-6.822, P〈0.001; 0.38±0.06 vs. 1.04±0.18, t=-7.778, P〈0.001; 0.29±0.04 vs. 1.06±0.12, t=-12.612, P〈0.001; 0.36±0.07 vs. 1.06±0.14, t=-10.000, P〈0.001; 0.43±0.08 vs. 0.97±0.12, t=-8.372, P〈0.001; 0.25±0.03 vs. 1.03±0.12, t=-14.100, P〈0.001; 0.19±0.03 vs. 0.99±0.13, t=-13.408, P〈0.001). The mRNA expression of Ecadherin was significantly higher than that in NCsiRNA group (2.88±0.42 vs. 0.98±0.12, t=9.726, P〈0.001). ConclusionKnockdown of Stat5 inhibits the invasion and EMT of thyroid carc
关 键 词:甲状腺肿瘤 肿瘤侵润 信号转导子和转录激活子5 上皮间质转化
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