FoxD3 deficiency promotes breast cancer progression by induction of epithelial-mesenchymal transition

被引:32
作者
Chu, Tian-Li [1 ]
Zhao, Hong-Meng [2 ,3 ]
Li, Yue [4 ]
Chen, Ao-Xiang [2 ,3 ]
Sun, Xuan [2 ,3 ]
Ge, Jie [2 ,3 ]
机构
[1] Peoples Hosp Wuqing, Dept Gen Surg, Tianjin, Peoples R China
[2] Tianjin Med Univ, Canc Inst & Hosp, Minist Educ, Key Lab Breast Canc Prevent & Treatment, Tianjin, Peoples R China
[3] Tianjin Med Univ, Canc Inst & Hosp, Tianjin, Peoples R China
[4] Med Coll Chinese Peoples Armed Police Force, Affiliated Hosp, Dept Respirat, Tianjin, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
Breast cancer; Epithelial-mesenchymal transition; FoxD3; TRANSCRIPTION FACTOR; PLURIPOTENCY; EXPRESSION; LINEAGE;
D O I
10.1016/j.bbrc.2014.03.019
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 transcription factor forkhead box 03 (FOXD3) plays an important role in the development of neural crest and gastric cancer cells. However, the function and mechanisms of FOXD3 in the breast tumorigenesis and progression is still limited. Here, we report that FOXD3 is a tumor suppressor of breast cancer tumorigenicity and aggressiveness. We found that FOXD3 is down-regulated in breast cancer tissues. Patients with low FOXD3 expression have a poor outcome. Depletion of FOXD3 expression promotes breast cancer cell proliferation and invasion in vitro, whereas overexpression of FOXD3 inhibits breast cancer cell proliferation and invasion both in vitro and in vivo. In addition, depletion of FOXD3 is linked to epithelial-mesenchymal transition (EMT)-like phenotype. Our results indicate FOXD3 exhibits tumor suppressive activity and may be useful for breast therapy. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:580 / 584
页数:5
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