The expression of Cullin1 is increased in renal cell carcinoma and promotes cancer cell proliferation, migration, and invasion

被引:13
作者
Ping, Ji-Gen [1 ]
Wang, Fei [1 ]
Pu, Jin-Xian [1 ]
Hou, Ping-Fu [2 ,3 ]
Chen, Yan-Su [2 ,3 ]
Bai, Jin [2 ,3 ]
Zheng, Jun-Nian [2 ,3 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, Dept Urol, Suzhou 215006, Jiangsu, Peoples R China
[2] Xuzhou Med Coll, Jiangsu Key Lab Biol Canc Therapy, 84 West Huaihai Rd, Xuzhou 221002, Jiangsu, Peoples R China
[3] Xuzhou Med Coll, Inst Canc, Jiangsu Ctr Collaborat & Innovat Canc Biotherapy, Xuzhou 221002, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Renal cell carcinoma; Cullin1; Tissue microarray; Cell progression; POOR-PROGNOSIS; SKP2; P27; METASTASIS; P27(KIP1);
D O I
10.1007/s13277-016-5151-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cullin1 (Cul1) is a scaffold protein of the ubiquitin E3 ligase Skp1/Cullin1/Rbx1/F-box protein complex, which ubiquitinates a broad range of proteins involved in cell-cycle progression, signal transduction, and transcription. To investigate the role of Cul1 in the development of renal cell carcinoma (RCC), we evaluated the Cul1 expression by immunohistochemistry using a tissue microarray (TMA) containing 307 cases of RCC tissues and 34 normal renal tissues. The Cul1 expression was increased significantly in RCC and was correlated with renal carcinoma histology grade (P = 0.007), tumor size (P = 0.013), and pT status (P = 0.023). Also, we found that silencing of Cul1 leads to increased expression of p21 and p27 that could inhibit the cyclin D-1 and cyclin E-2 expressions and arrest cell cycle at the G1 phase. Furthermore, knockdown of Cul1 inhibits RCC cell migration and invasion abilities by up-regulating the expression of TIMP-1 which could inhibit the expression of MMP-9. Finally, using bioluminescence imaging, we found that Cul1 knockdown significantly reduced the tumor growth in vivo. Cul1 may constitute a potential therapeutic target in RCC.
引用
收藏
页码:12823 / 12831
页数:9
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