Circular RNA circRPPH1 promotes triple-negative breast cancer progression via the miR-556-5p/YAP1 axis

被引:2
作者
Zhou, Yehui [1 ,2 ]
Liu, Xiaorong [1 ,3 ]
Lang, Jing [2 ]
Wan, Yuqiu [2 ]
Zhu, Xun [1 ]
机构
[1] Soochow Univ, Affiliated Hosp 2, Dept Gen Surg, 1055 Sanxiang Rd, Suzhou 215004, Jiangsu, Peoples R China
[2] Soochow Univ, Affiliated Hosp 1, Dept Gen Surg, Suzhou 215006, Jiangsu, Peoples R China
[3] Jiaxing Univ, Affiliated Hosp 2, Dept Gen Surg, 1518 North Huancheng Rd, Jiaxing 314000, Zhejiang, Peoples R China
来源
AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH | 2020年 / 12卷 / 10期
关键词
Breast cancer; miRNA sponge; circRPPH1; miR-556-5p; YAP1; YES-ASSOCIATED PROTEIN; HIPPO PATHWAY; YAP; METASTASIS; SUPPRESSOR; EXPRESSION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Circular RNAs (circRNAs), which are considered to be important functional regulators in cancer, have provided a new perspective regarding our understanding of tumor biology, including that of breast cancer. To investigate the regulatory effect of circRPPH1 on cellular behaviors of breast cancer and the potential mechanism, the expression of circRPPH1 and miR-556-5p in breast cancer tissues and cell lines were examined by quantitative RT-PCR. The regulatory effects of the circRPPH1/miR-556-5p/YAP1 axis on cellular behaviors of breast cancer cells were evaluated through functional experiments in vitro and tumor growth in vivo. The relationship between circRPPH1 and miR-556-5p/YAP1 was assessed using dual-luciferase reporter and RNA immunoprecipitation assays. PCR results showed that circRPPH1 levels were significantly upregulated in tumor tissues and breast cancer cells. Functionally, circRPPH1 promoted the proliferation, migration, invasion, and angiogenesis of breast cancer cell lines and tumor growth in vivo. Regarding the mechanism, dual-luciferase reporter and RNA immunoprecipitation assays showed that circRPPH1 was capable of sponging miR-556-5p to increase expression of the oncogene YAP1. Our data reveal that circRPPH1 plays a vital regulatory role in breast cancer via the miR-556-5p/YAP1 axis and may serve as a promising therapeutic target for breast cancer treatment.
引用
收藏
页码:6220 / 6234
页数:15
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