CSN6 promotes the cell migration of breast cancer cells by positively regulating Snail1 stability

被引:7
|
作者
Mou, Jie [1 ,2 ,3 ]
Wei, Lulu [1 ,4 ,5 ]
Liang, Jia [1 ]
Du, Wenqi [6 ]
Pei, Dongsheng [1 ]
机构
[1] Xuzhou Med Univ, Dept Pathol, Xuzhou, Jiangsu, Peoples R China
[2] Xuzhou Med Univ, Jiangsu Key Lab New Drug & Clin Pharm, Xuzhou, Jiangsu, Peoples R China
[3] Xuzhou Med Univ, Sch Pharm, Xuzhou, Jiangsu, Peoples R China
[4] Nanjing Univ, Ctr Translat Med, Med Sch, Nanjing, Peoples R China
[5] Nanjing Univ, Jiangsu Key Lab Mol Med, Med Sch, Nanjing, Peoples R China
[6] Xuzhou Med Univ, Dept Human Anat, Xuzhou, Jiangsu, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
CSN6; Snail1; cell migration; breast cancer; COP9; SIGNALOSOME; DOWN-REGULATION; E-CADHERIN; EXPRESSION; DEGRADATION; CARCINOMA; EMT; PHOSPHORYLATION; METASTASIS; MECHANISMS;
D O I
10.7150/ijms.50206
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: CSN6, a subunit of the highly conserved constitutive photomorphogenesis 9 (COP9) signalosome (CSN), has been reported to be implicated in tumor progression in various kinds of malignant tumors. However, the mechanism underlying CSN6 in the tumor development of breast cancer has not yet been fully elucidated. Methods: CSN6 staining in breast cancer tissues and paracancerous tissues was measured by tissue microarray (TMA) technology. The metastatic effect of CSN6 was measured by cell migration assay. Co-immunoprecipitation study was used to show the interaction between the protein CSN6 and Snail1. Ubiquitination assay was performed to validate whether ubiquitination is involved in the upregulation of Snail1 by CSN6. The impact of CSN6 on tumor metastasis in vivo was analyzed using xenotransplantation experiments in BALB/c mice. Results: Here, we demonstrated that CSN6 expression was dramatically increased in breast cancer tissues compared with paired adjacent cancerous tissues. CSN6 promoted the cell migration and wound healing abilities in breast cancer cell lines. Also we showed that CSN6 associates with Snail1 and enhances Snail1 protein level by inhibiting the ubiquitin-mediated degradation of Snail1. Thus, CSN6 is involved in positively regulating the stability of Snail1. We further proved that CSN6 protein level was positively correlated with the Snail1 expression in xenograft model. Conclusion: These findings provide new insight into applicability of using the CSN6-Snail1 axis as a potential therapeutic target in breast cancer.
引用
收藏
页码:2809 / 2818
页数:10
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