摘要
目的:探讨hsa-miR-518b反义寡核苷酸(Antisense oligonucleotide,ASODN)对胃癌细胞生长和细胞周期的影响,以分析其在胃癌中的作用机制。方法:设计合成全硫代磷酸化修饰的hsa-miR-518b ASODN,将其转染于胃癌细胞株SGC7901。用Realtime RT-PCR分析hsa-miR-518b在胃癌细胞转染前后的表达情况,MTT检测胃癌细胞转染后的生长情况,流式细胞仪分析细胞周期。结果:转染hsa-miR-518b ASODN后,胃癌细胞hsa-miR-518b表达显著降低(P=0.000),生长受到抑制(P=0.000),大量胃癌细胞阻滞于G1期(P=0.000)。结论:hsa-miR-518b ASODN能使胃癌细胞阻滞于G1期,抑制胃癌细胞的生长。提示hsa-miR-518b可能通过促进细胞周期G1/S期转换而促进胃癌细胞生长。
Objective:To investigate the effects of antisense oligonucleotide(ASODN ) targeting hsa-miR-518b on the growth and cycle of gastric cancer cell, and the mechanism in gastric cancer. Methods: Specific phosphorothioate antisense oligodeoxynucleotides targeting hsa-miR-51gb were synthesized and then transfected into the gastric cancer cell( SGC7901 ). We investigated the change of the hsa-miR-518b expression in SGC7901 after the transfection by using real time RT-PCR.Methyl thiazolyl tetrazolium (MTT)assay was used to detect the cell growth of SGC 7901 and fluorescence activated cell sorting (FACS)was used to analyze the cell cycle of SGC7901. Results : After transfection, the expression of hsa-miR-518b was decrased (P=0.000), the growth of SGC7901 was suppressed (P=-0.000) and the cell cycle arrested in Gl (P=0.000). Conclusion: hsa-miR-518b (ASODN)could suppress the growth of SGC 7901 by arresting the cell cycle in G1 phase. Hsa-miR-518b could promote the growth of gastric cancer cell by regulating C1/S transition.
出处
《重庆医科大学学报》
CAS
CSCD
北大核心
2009年第5期567-569,共3页
Journal of Chongqing Medical University