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特异性miR-221抑制剂对结直肠癌细胞增殖及凋亡的影响

王伟 孙凯 吴承堂 雷尚通 曾俊杰 伍颖君 李国新

南方医科大学学报2011,Vol.31Issue(4):674-677,4.
南方医科大学学报2011,Vol.31Issue(4):674-677,4.

特异性miR-221抑制剂对结直肠癌细胞增殖及凋亡的影响

APPLICATION OF INTEGRATED GEOPHYSICAL TECHNIQUE IN BASEMENT STRUCTURE RESEARCH IN BINBEI AREA

王伟 1孙凯 1吴承堂 1雷尚通 1曾俊杰 1伍颖君 1李国新1

作者信息

  • 1. 南方医科大学南方医院普通外科,广东广州510515
  • 折叠

摘要

Abstract

Objective To investigate miRNA-221 expression in human colorectal carcinoma (CRC) cells and the effects of miR-221-specific inhibitor on the proliferation and apoptosis of CRC cells. Methods Four human CRC cell lines (HT-29, Lovo, SW-480, and CaCO2) were examined for miRNA-221 expression using real-time Q-PCR. The specific 2-methoxy-modified RNA oligonucleotides of miR-221 (anti-miR-221) were synthesized and transfected into Caco2 cells via liposome, and the changes in the expression of miR-221 in the cells were detected by real-time Q-PCR. The proliferation and apoptosis of the transfected CRC cells were detected using MTT assay and flow cytometry. Results The 4 human CRC cells showed significantly upregulated expression of mtR-221 compare with HUVECs (P< 0.01). The miR-221-specific inhibitor, anti-miR-221, significantly inhibited the expression of miR-221 in Caco2 cells and suppressed the cell proliferation, causing also obvious cell apoptosis (P<0.01). Conclusion The miR-221-specific inhibitor shows potent inhibitory effect on the growth of CRC cells, suggesting its value as a potential anti-tumor candidate for treatment of CRC.

关键词

结直肠癌/miRNA-221/增殖/凋亡

Key words

colorectal carcinoma/ miRNA-221/ proliferation/ apoptosis

分类

医药卫生

引用本文复制引用

王伟,孙凯,吴承堂,雷尚通,曾俊杰,伍颖君,李国新..特异性miR-221抑制剂对结直肠癌细胞增殖及凋亡的影响[J].南方医科大学学报,2011,31(4):674-677,4.

基金项目

广东省自然科学基金博士启动项目(8451051501000390) (8451051501000390)

广东省医学科研基金(B2010190) (B2010190)

南方医科大学南方医院院长基金(2008C005) (2008C005)

南方医科大学学报

OA北大核心CSCDCSTPCDMEDLINE

1673-4254

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