基础医学与临床 ›› 2009, Vol. 29 ›› Issue (8): 850-854.

• 研究论文 • 上一篇    下一篇

骨桥蛋白反义核酸抑制乳腺癌细胞系增殖和诱导其凋亡

周云松 温晓辉 杨林西 陈朋   

  1. 西北民族大学医学院 兰州大学基础医学院
  • 收稿日期:2007-12-13 修回日期:2008-10-14 出版日期:2009-08-20 发布日期:2009-08-20
  • 通讯作者: 周云松

OPN antisense oligodeoxynucleotide inhibits proliferation and apoptosis of human breast carcinoma cell line

Yun-song ZHOU, Xiao-hui WEN, Lin-xi YANG, Peng CHEN   

  1. Medical School of Northwest University for Nationalities School of Basic Medical Sciences, Lanzhou University
  • Received:2007-12-13 Revised:2008-10-14 Online:2009-08-20 Published:2009-08-20
  • Contact: Yun-song ZHOU,

摘要: 目的 观察结合于骨桥蛋白(OPN) mRNA上低自由能区域的反义寡脱氧核苷酸(ASODN)对OPN基因的抑制效应,以及对人乳腺癌细胞系MCF-7细胞体外增殖和凋亡的影响。方法 基于最小自由能算法,针对OPN mRNA上的低结合自由能区域设计合成ASODN,转染高表达OPN的人乳腺癌细胞系MCF-7;MTT法测定细胞增殖抑制率;电子显微镜下观察细胞形态学改变;RT-PCR检测OPN mRNA水平;流式细胞术检测细胞周期及凋亡发生率。结果 OPN ASODN呈时间和剂量依赖性抑制MCF-7细胞增殖 (P<0.05);经16?mol/LOPN ASODN作用72h,细胞呈典型凋亡特征; OPN mRNA表达水平下降;反义组凋亡细胞比例显著升高(P<0.01)。结论OPN ASODN在体外可抑制人乳腺癌MCF-7细胞增殖并诱导其发生凋亡;利用最小自由能原理来设计反义寡核苷酸是一种较为可靠的方法。

关键词: 骨桥蛋白, 反义寡核苷酸, 自由能, 乳腺癌, 调亡

Abstract: Objective To investigate the effects on anti-expression of Osteopontin (OPN) by an antisense oligodeoxynucleotide (ASODN) targeting to low free energy region of OPN mRNA and its effects on proliferation and apoptosis of human breast carcinoma cell line MCF-7. Methods Designing and synthesizing an ASODN based on minimum free energy algorithm in vitro, which targets to the low free energy region of OPN mRNA. Transfecting it into breast carcinoma cell line MCF-7 which expresses OPN in high level. The cell proliferation-inhibitory rate was determined by MTT method; The morphologic changes was observed by transmission electron microscope (TEM); The OPN mRNA expression level was checked by RT-PCR method; Cell cycle and apoptosis rate were detected by flow cytometry (FCM) after transfection ,respectively. Results OPN ASODN could inhibit the proliferation of the cells in both time and concentration dependent manner (P<0.05).Characteristic morphologic apoptosis changes was observed after incubated with 16?mol/L OPN ASODN for 72h. OPN mRNA expression in ASODN groups were notably decreased. there was a significant high apoptosis rate in ASODN groups (P<0.01). Conclusions OPN ASODN transfection significantly inhibits the proliferation of human breast carcinoma MCF-7 cells and induces cell apoptosis in vitro. It's a reliable method to design ASODN based on minimum free energy algorithm.

Key words: Osteopontin, Antisense oligodeoxynucleotide, Free energy, Breast carcinoma, Apoptosis