Effects of miR-93 antisense oligonucleotides on cell proliferation and apoptosis in breast cancer
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Effects of miR-93 antisense oligonucleotides on cell proliferation and apoptosis in breast cancer
Journal of Chongqing Medical UniversityVol. 38, Issue 3, Pages: 396-400(2014)
作者机构:
1. 南昌市第三医院乳腺外科,南昌,330009
2. 江西省肿瘤医院乳腺外科,南昌,330029
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Published:2014,
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Luo Ping, Zhong Xiaoming, Xie Chunwei. Effects of miR-93 antisense oligonucleotides on cell proliferation and apoptosis in breast cancer. [J]. Journal of Chongqing Medical University 38(3):396-400(2014)
DOI:
Luo Ping, Zhong Xiaoming, Xie Chunwei. Effects of miR-93 antisense oligonucleotides on cell proliferation and apoptosis in breast cancer. [J]. Journal of Chongqing Medical University 38(3):396-400(2014)DOI:
Effects of miR-93 antisense oligonucleotides on cell proliferation and apoptosis in breast cancer
Objective:To investigate the expression of miR-93 in breast cancer tissues and to explore the regulative effects of miR-93 antisense oligonucleotide(ASO) on the proliferation and apoptosis of breast cancer cells. Methods:Expression of miR-93 in 120 breast cancer tissues and their adjacent tissues was detected by real-time quantitative PCR. After transfection with miR-93 ASO,biological effects of miR-93 on breast cancer cells were measured by MTT assay,colony formation experiment and flow cytometry. Results:Expression of miR-93 was higher in 63.33%(76/120) breast cancer tissues than in adjacent tissues(P<0.05). miR-93 ASO could reduce the expression of miR-93 significantly(P<0.05). MTT assay results showed that breast cancer cells survival rate at 24,48,96 h decreased greatly after transfection with miR-93 ASO(P<0.05). Clone formation assay revealed that colony formation rate was significantly lower in miR-93 ASO group than in blank control group and nonsense interference group(P<0.05). Flow cytometry indicated that the apoptotic index was significantly higher in miR-93 ASO group than in two control groups(P<0.05). In addition,Bcl2 mRNA and protein levels were significantly decreased after reducing expression of miR-93. Conclusions:miR-93 is overex-pressed in the human breast cancer. Reducing expression of miR-93 can effectively inhibit the growth of breast cancer cells and pro-mote apoptosis . miR-93 may become a new target for the regulation of gene expression in breast cancer.