Effect of antisense miR-18a on invasion and migration in breast cancer cells
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Effect of antisense miR-18a on invasion and migration in breast cancer cells
Journal of Chongqing Medical UniversityVol. 38, Issue 3, Pages: 391-395(2014)
作者机构:
南昌市第三医院乳腺外科,南昌,330009
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Published:2014,
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Chen Ge, Luo Ping, Gong Yu, et al. Effect of antisense miR-18a on invasion and migration in breast cancer cells. [J]. Journal of Chongqing Medical University 38(3):391-395(2014)
DOI:
Chen Ge, Luo Ping, Gong Yu, et al. Effect of antisense miR-18a on invasion and migration in breast cancer cells. [J]. Journal of Chongqing Medical University 38(3):391-395(2014)DOI:
Effect of antisense miR-18a on invasion and migration in breast cancer cells
Objective:To investigate the expression of miR-18a in breast cancer tissues and to explore the regulative effects of miR-18a antisense oligonucleotide(ASO) on the invasion and migration of breast cancer cells in vitro. Methods:The expression of miR-18a in 108 breast cancer tissues and their adjacent breast tissues were detected by real-time quantitative PCR method. After trans-fection with miR-18aASO,the biological effects of miR-18a on breast cancer cells was measured by Transwell assay and wound healing assay and invasion-related protein expression was analyzed by Western blot. Results:miR-18a was found to be overexpressed in 50.93%(55/108) of the breast cancer cases(t=28.68,P=0.000). miR-18a expression in breast cancer cells(transfection with miR-18a ASO) was significantly less than that of control group(F=321.67,P=0.001;F=563.28,P=0.000). Transwell and wound healing as-say results showed that the invasion and migration ability decreased greatly after the transfection with miR-18a ASO(P=0.000),fur-thermore,down-regulation of miR-18a resulted in obvious inactivation of matrix metalloproteinase(MMP)2 and MMP9(P=0.000). Conclusions:miR-18a is overexpressed in human breast cancer. Reducing the expression of miR-18a can effectively inhibit the inva-sion and migration of breast cancer cells. miR-18a may become a new target for the regulation of invasion and migration in breast can-cer.