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出 处:《中国临床新医学》2009年第6期545-548,共4页CHINESE JOURNAL OF NEW CLINICAL MEDICINE
基 金:国家自然科学基金资助项目(No30360111)
摘 要:目的利用小干扰RNA(small interfering RNA,siRNA)抑制人舌癌Tca883细胞血管内皮生长因子(vascular endothelial growth factor,VEGF)表达,观察其对培养细胞和移植瘤基质金属蛋白酶-9(matrix metalloproteinase-9,MMP-9)蛋白表达的影响。方法以稳定转染携带VEGF—siRNA真核表达载体的人舌癌Tca8113细胞(VEGF—siRNA1、VEGF—siRNA2)为实验组,以转染空载体人舌癌Tca8113细胞及未转染的人舌癌Tea8113细胞为实验对照组和空白对照组,将各组细胞分别接种于裸鼠皮下,用免疫细胞/组织化学法分别测定各组培养细胞和移植瘤VEGF及MMP-9的蛋白表达。结果在培养细胞和移植瘤中,与实验对照组和空白对照组相比,VEGF—siRNA1组和VEGF—siRNA2组VEGF染色平均灰度值高,差异有统计学意义(P〈0.05);各组培养细胞中均未见MMP-9表达;各组移植瘤MMP-9染色平均灰度值之间的差异无统计学意义(P〉0.05)。结论以siRNA干扰沉默人舌癌Tca8113细胞VEGF基因,可明显抑制细胞及移植瘤内VEGF蛋白表达,但是对MMP-9蛋白的表达无明显影响。Objective To investigate the expression of matrix metalloproteinase -9 (MMP -9) in human tongue squamous cell carcinoma( Tca8113 )in vitro and in vivo, after the expression of vascular endothelial growth fac- tor(VEGF) suppressed by vector- based small interfering RNA (siRNA). Methods The eukaryotic expression vec- tor taken as an experimental control and two siRNA targeting VEGF constructed in the vector ( VEGF - siRNA1, VEGF- siRNA2) were transfected into human tongue squamous cell carcinoma cell lines (Tca8113). The non- transfected Tca8113 cells were used as negative control. The transfected cells and non- transfected cells were injec- ted subcutaneously on the back of the twenty nude - mice which were divided into four groups randomly ( n -- 5/ group), respectively. The expression of VEGF and MMP - 9 in the cultured ceils and the xenograft tumors were de- tected by immunocytochemistry and immunohistochemistry. Results Compared with the experimental and negative controls, the VEGF expressions were decreased (P 〈 0.05 ) in two experimental groups of the cultured cells and xen- ograft tumors. There was no obvious MMP - 9 staining in four groups of cultured cells. There were no significant differences of the MMP - 9 expression among four groups of xenograft tumor ( P 〉 0. 05 ). Conclusion VEGF - siR- NA can down - regulate the expression of VEGF in the human tongue squamous cell carcinoma in vitro and in vivo. However, it may not influence on the expression of MMP -9 efficiently.
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