SOX5 promotes breast cancer proliferation and invasion by transactivation of EZH2

被引:29
|
作者
Sun, Chuntao [1 ]
Ban, Yunqing [2 ]
Wang, Kai [3 ]
Sun, Yanming [1 ]
Zhao, Zhihua [4 ]
机构
[1] Weifang City Peoples Hosp, Dept Intervent Radiol, Weifang 261041, Shandong, Peoples R China
[2] Xinjiang Med Univ, Imaging Ctr, Affiliated Hosp 5, Urumqi 830011, Xinjiang, Peoples R China
[3] Weifang City Peoples Hosp, Dept Breast Surg, 151 Guangwen St, Weifang 261041, Shandong, Peoples R China
[4] Weifang City Peoples Hosp, Dept Nucl Med, Weifang 261041, Shandong, Peoples R China
关键词
sex determining region Y-box protein 5; enhancer of zeste 2 polycomb repressive complex 2 subunit; breast cancer; proliferation; invasion; EPITHELIAL-MESENCHYMAL TRANSITION; EXPRESSION; GENE; PROGRESSION;
D O I
10.3892/ol.2019.9914
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Sex determining region Y-box protein 5 (SOX5) is a transcriptional factor and serves important roles in various cancer types; however, the pathological role of SOX5 in patients with breast cancer remains unclear. In the present study, the expression and potential role of SOX5 in patients with breast cancer and in breast cancer cells was investigated. The data indicated that SOX5 was highly expressed in breast cancer tissues compared with adjacent healthy tissues, and overexpression of SOX5 was associated with a reduced overall survival rate in patients with breast cancer. Gain and loss of function studies with MTT, colony formation, wound healing and Matrigel invasion assays demonstrated that SOX5 significantly promoted breast cancer cell proliferation and invasion. The chromatin immunoprecipitation (ChIP) assay sequence, quantitative ChIP and luciferase reporter assays were used to identify enhancer of zeste 2 polycomb repressive complex 2 subunit (EZH2) as a downstream target gene of SOX5. Furthermore, it was determined that ectopic expression of SOX5 increased EZH2 expression at the mRNA and protein level, while the knockdown of SOX5 decreased EZH2 expression. Additionally, the biological effect of SOX5 was investigated, and it was determined to be dependent on the regulation of EZH2 expression. The present results may provide important insights into the biological significance of SOX5 serving as a candidate therapeutic target in breast cancer progression.
引用
收藏
页码:2754 / 2762
页数:9
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