RETRACTED: Inhibition of breast cancer metastasis with microRNA-302a by downregulation of CXCR4 expression (Retracted article. See vol. 196, pg. 665, 2022)

被引:45
作者
Liang, Zhongxing [1 ,2 ]
Bian, Xuehai [1 ,3 ]
Shim, Hyunsuk [1 ,2 ]
机构
[1] Emory Univ, Dept Radiol & Imaging Sci, Atlanta, GA 30322 USA
[2] Emory Univ, Winship Canc Inst, Atlanta, GA 30322 USA
[3] Jilin Univ, Dept Thyroid Surg, China Japan Union Hosp, Changchun 130023, Peoples R China
关键词
MicroRNA; Breast cancer; Metastasis; CXCR4; CELLS; TUMOR; CLUSTER; GROWTH; GENE; ANGIOGENESIS; MIR-302-367; TARGETS; BLOCKS; LIGAND;
D O I
10.1007/s10549-014-3053-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metastasis remains a main cause of mortality from breast cancer and an unresolved issue. The purpose of this study is to investigate the role of miR-302a in the development of breast cancer metastasis mediated by CXCR4, a critical regulator of metastasis, and to identify miR-302a as an effective therapeutic agent for therapy and prevention of breast cancer metastasis. Our studies show that miR-302a expression levels were downregulated in metastatic breast cancer cells and tumor tissues. Additionally, the expression levels of miR-302a were inversely correlated with CXCR4 levels. More promisingly, miR-302a inhibited the invasion and metastasis of breast cancer cells in vitro and in vivo and reduced the expression of CXCR4. Our findings demonstrated that the repression of miR-302a levels contributes to breast cancer metastasis and restoration of miR-302a baseline expression inhibits the invasion and metastasis of breast cancer cells. These data suggest that miR-302a mimics are potential therapeutic agents for breast cancer metastasis.
引用
收藏
页码:535 / 542
页数:8
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