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作 者:赵义[1] 张尤历[1] 王国英[1] 张行行[1] 龚爱华[2] 葛璐[1] 李杰[1] 倪鑫[1] 刘鑫[1] 徐岷[1]
机构地区:[1]江苏大学附属医院消化病科,212001 [2]江苏大学医学院
出 处:《江苏医药》2015年第17期1991-1994,F0002,共5页Jiangsu Medical Journal
基 金:江苏省卫生厅科研资助项目(H201434);镇江市科技支撑计划资助项目(SH2014024)
摘 要:目的探讨尿路上皮癌胚抗原1(UCA-1)在胰腺癌细胞侵袭转移中的作用。方法采用实时荧光定量PCR检测5株胰腺癌细胞长链非编码核糖核酸UCA-1的表达;采用UCA-1表达质粒提高PaTu8988细胞的UCA-1水平,小干扰RNA用于降低BxPC-3细胞的UCA-1表达。用Transwell侵袭实验和迁移实验观察转染后的PaTu8988细胞和BxPC-3细胞的侵袭和迁移能力变化,Western blot检测基质金属蛋白酶2(MMP-2)和MMP-9的表达。结果 UCA-1差异性表达于5株胰腺癌细胞。过表达UCA-1后,PaTu8988细胞的MMP-2和MMP-9的蛋白水平均增加,侵袭和迁移能力增强(P<0.001);而干扰UCA-1后,BxPC-3细胞的MMP-2和MMP-9的蛋白表达均降低,侵袭和迁移能力减弱(P<0.001)。结论 UCA-1的高表达能增强胰腺癌细胞的体外侵袭转移能力。Objective To explore the role of long noncoding RNA urothelial carcinoma antigen 1 (UCA1) in the invasion and metastasis of pancreatic cancer cells. Methods The expressions of UCA1 in 5 pancreatic cancer cell lines were analyzed by qRT PCR, The UCA1 plasmid was used to overexpress the UCA-1 in PaTu8988 cells. The level of UCA-1 in BxPC-3 cells was knocked down by small interfering RNA(siRNA). The capacity of invasion and migration in vitro of transfeeted PaTu8988 and BxPC-3 cells was tested by Transwell invasion assay and migration assay. The protein levels of matrix metalloproteinase 2(MMP-2) and MMP-9 were examined by Western blot. Results UCA-1 was differentially expressed in 5 pancreatic cancer cell lines. Upregulation of UCA-1 increased the levels of MMP-2 and MMP-9 and enhanced the ability of invasion and migration of PaTu8988 cells. Downregulation of UCA-1 decreased the expressions of MMP-2 and MMP-9 and impaired the capacity of invasion and migration of BxPC-3 cells(P^0. 001). Conclusion The overexpression of UCA-1 can enhance the ability of invasion and metastasis in vitro of pancreatic cancer ceils.
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