MiR-539 inhibits the malignant behavior of breast cancer cells by targeting SP1

被引:23
作者
Cai, Fenglin [1 ,2 ]
Chen, Luhong [1 ,2 ]
Sun, Yuting [1 ,2 ]
He, Chunlan [1 ,2 ]
Fu, Deyuan [1 ,2 ]
Tang, Jinhai [3 ]
机构
[1] Yangzhou Univ, Clin Med Coll, Dept Gen Surg, Yangzhou 225001, Jiangsu, Peoples R China
[2] Northern Jiangsu Peoples Hosp, Yangzhou 225001, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Affiliated Hosp 1, Dept Gen Surg, Nanjing 210029, Peoples R China
关键词
miR-539; breast cancer; SP1; LUNG-CANCER; EXPRESSION; CARCINOMA; MIRNAS; PROGRESSION; BIOMARKERS; RESISTANCE; MICRORNAS; INVASION; PATHWAY;
D O I
10.1139/bcb-2019-0111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aberrant expression of microRNAs (miRNAs) is involved in the initiation and progression of human cancers. In our study, we found that miR-539 was down-regulated in breast cancer tissues and cell lines. Decreased expression of miR-539 was significantly associated with lymph node metastasis in patients with breast cancer. Overexpression of miR-539 inhibited the proliferation and promoted apoptosis of breast cancer cells. Moreover, highly expressed miR-539 significantly suppressed the epithelial-mesenchymal transition (EMT) and sensitized cells to cisplatin treatment. Mechanistically, miR-539 was found to target the specificity protein 1 (SP1) and down-regulated the expression of SP1 in breast cancer cells. Knockdown of miR-539 consistently increased the expression of SP1. The expression of miR-539 in breast cancer tissues was negatively correlated with the expression of SP1. Restoration of SP1 significantly attenuated the inhibitory effect of miR-539 on the proliferation of breast cancer cells. Taken together, our results indicate that miR-539 has a tumor suppressive role in breast cancer via targeting SP1, suggesting miR-539 as a promising target for the diagnosis of breast cancer.
引用
收藏
页码:426 / 433
页数:8
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