Inhibition of cell invasion and migration by CEACAM1-4S in breast cancer

被引:11
作者
Yang, Changcheng [1 ,4 ]
Cao, Manlin [2 ]
Liu, Yiwen [1 ]
He, Yiqing [1 ]
Yang, Cuixia [1 ]
Du, Yan [1 ]
Wang, Wenjuan [1 ]
Zhang, Guoliang [1 ]
Wu, Man [1 ]
Zhou, Muqing [1 ]
Gao, Feng [3 ]
机构
[1] Shanghai Jiao Tong Univ, Affiliated Peoples Hosp 6, Dept Mol Biol, Shanghai 200233, Peoples R China
[2] Shanghai Jiao Tong Univ, Affiliated Peoples Hosp 6, Dept Rehabil Med, Shanghai 200233, Peoples R China
[3] Shanghai Jiao Tong Univ, Affiliated Peoples Hosp 6, Dept Mol Biol & Clin Lab, 600 Yishan Rd, Shanghai 200233, Peoples R China
[4] Zhengzhou Univ, Affiliated Canc Hosp, Dept Med Oncol, Henan Canc Hosp, Zhengzhou 450008, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
carcinoembryonic antigen-related cell adhesion molecule 1-4S; breast cancer; invasion; migration; balanced regulation; epithelial-mesenchymal transition; ADHESION MOLECULE; TUMOR-SUPPRESSOR; BILIARY GLYCOPROTEIN; MATRIX METALLOPROTEINASES; GENE-EXPRESSION; DOWN-REGULATION; ANTIGEN FAMILY; CD66A BGP; GROWTH; ANGIOGENESIS;
D O I
10.3892/ol.2017.6791
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1), a cell-cell adhesion molecule, has been revealed to perform an important role in tumor progression. Although there are a number of studies on CEACAM1 in patients with breast cancer, there is limited information on the roles of CEACAM1 in breast cancer metastasis. The present study aimed to identify whether CEACAM1 is involved in breast cancer development and to investigate the underlying mechanisms. First, the expression of CEACAM1 was observed in patients with breast cancer, and the association between CEACAM1 expression levels and migration and invasion of breast cancer cells was analyzed. As there are 12 isoforms of CEACAM1, of which CEACAM1-4S dominates in the human breast epithelium, subsequent study focused on CEACAM1-4S as a representative of all the isoforms. Results of the present study demonstrated that CEACAM1-4S suppresses breast cancer cell invasion and migration in a manner that is dependent on the balance between matrix metalloproteinase 2/tissue inhibitor of metalloproteinase 2 and E-/N-cadherin expression. In addition, CEACAM1-4S was likely to cause reversal of epithelial-mesenchymal transition of breast cancer cells through repressing Smad2 and signal transducer and phosphorylation of activator of transcription 3. In conclusion, the present study demonstrated that CEACAM1-4S performs an inhibitory role in breast cancer metastasis, and restoring CEACAM1-4S expression may provide a novel strategy for therapy of patients with metastatic breast cancer.
引用
收藏
页码:4758 / 4766
页数:9
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