Skp2 is over-expressed in breast cancer and promotes breast cancer cell proliferation

被引:48
作者
Zhang, Wenwen [1 ]
Cao, Lulu [1 ]
Sun, Zijia [1 ]
Xu, Jing [1 ]
Tang, Lin [1 ]
Chen, Weiwei [1 ]
Luo, Jiayan [1 ]
Yang, Fang [1 ]
Wang, Yucai [2 ]
Guan, Xiaoxiang [1 ,3 ]
机构
[1] Nanjing Univ, Sch Med, Jinling Hosp, Dept Med Oncol, 305 East Zhongshan Rd, Nanjing 210002, Jiangsu, Peoples R China
[2] Rutgers New Jersey Med Sch, Dept Med, Newark, NJ USA
[3] Nanjing Med Univ, Jinling Hosp, Dept Med Oncol, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
breast cancer; PHB; PIG3; prognosis; proliferation; p53; Skp2; Skp2B; DEGRADATION; P27(KIP1); P53; PHOSPHORYLATION; CONTRIBUTES; APOPTOSIS; GENE; PIG3; UBIQUITINATION; DEREGULATION;
D O I
10.1080/15384101.2016.1160986
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The F box protein Skp2 is oncogenic. Skp2 and Skp2B, an isoform of Skp2 are overexpressed in breast cancer. However, little is known regarding the mechanism by which Skp2B promotes the occurrence and development of breast cancer. Here, we determined the expression and clinical outcomes of Skp2 in breast cancer samples and cell lines using breast cancer database, and investigated the role of Skp2 and Skp2B in breast cancer cell growth, apoptosis and cell cycle arrest. We obtained Skp2 is significantly overexpressed in breast cancer samples and cell lines, and high Skp2 expression positively correlated with poor prognosis of breast cancer. Both Skp2 and Skp2B could promote breast cancer cell proliferation, inhibit cell apoptosis, change the cell cycle distribution and induce the increased S phase cells and therefore induce cell proliferation in breast cancer cells. Moreover, the 2 isoforms could both suppress PIG3 expression via independent pathways in the breast cancer cells. Skp2 suppressed p53 and inhibited PIG3-induced apoptosis, while Skp2B attenuated the function of PIG3 by inhibiting PHB. Our results indicate that Skp2 and Skp2B induce breast cancer cell development and progression, making Skp2 and Skp2B potential molecular targets for breast cancer therapy.
引用
收藏
页码:1344 / 1351
页数:8
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