Expression and significance of Cystatin-C in clear cell renal cell carcinoma

被引:17
|
作者
Guo, Kunbin [1 ]
Chen, Qiuhong [2 ]
He, Xiaobo [3 ]
Yao, Kai [2 ]
Li, Zhiyong [2 ]
Liu, Zefu [2 ]
Chen, Jieping [2 ]
Liu, Zhuowei [2 ]
Guo, Chao [4 ]
Lu, Jiabin [5 ]
Wu, Chenyan [5 ]
Li, Weirong [1 ]
Wang, Qi [1 ]
Chen, Ping [6 ]
Lu, Wenhua [6 ]
Wang, Yongqiang [2 ,7 ]
Han, Hui [2 ]
Cao, Yun [5 ]
Guo, Shengjie [2 ]
机构
[1] Guangzhou Univ Chinese Med, Inst Clin Pharmacol, Guangzhou 510060, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Dept Urol, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China,Canc Ctr, Guangzhou 510060, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Dept Med Oncol, Affiliated Hosp 5, Zhuhai 519000, Peoples R China
[4] Guangdong Med Univ, Dept Plast Surg, Zhanjiang 524001, Guangdong, Peoples R China
[5] Sun Yat Sen Univ, Collaborat Innovat Ctr Canc Med, Dept Pathol, State Key Lab Oncol South China,Canc Ctr, Guangzhou 510060, Guangdong, Peoples R China
[6] Sun Yat Sen Univ, Collaborat Innovat Ctr Canc Med, State Key Lab Oncol South China, Canc Ctr, Guangzhou 510060, Guangdong, Peoples R China
[7] Univ Calif Davis, Sch Med, Dept Biochem & Mol Med, Sacramento, CA 95817 USA
基金
中国国家自然科学基金;
关键词
Cystatin-C; CRISPR/Case; 9; Clear cell renal cell cancer; Biomarker; CYSTEINE PROTEASE INHIBITORS; SIGNALING PATHWAY; CATHEPSINS B; NITRIC-OXIDE; STEFIN B; CANCER; GROWTH; ANGIOGENESIS; TISSUE; SERA;
D O I
10.1016/j.biopha.2018.08.083
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Purpose: Cystatin-C (Cys-C) has been studied as a valuable prognostic indicator in several malignancies. The goal of this study is to explore the expression and prognostic significance of Cys-C in clear cell renal cell carcinoma (CCRCC). Methods: Immunohistochemistry and western blot assays were performed to evaluate the level of Cys-C expression in CCRCC tissue. Expression levels of Cys-C in CCRCC tissue samples in relation to clinicopathological characteristics of the tumors were assessed. Their prognostic significance was analyzed by univariate and multivariate analyses. In addition, the expression of Cys-C in 786-O cell lines was inhibited by using CRISPR/Case9 and the effects of Cys-C knockout on 786-O cells in vitro were evaluated using MTT method, colony formation assay, cell cycle assay, and cell migration and invasive assay. Results: The expression level of Cys-C was lower in CCRCC tissues (n=253) than in paired adjacent non-cancerous tissues (n=164) by immunohistochemistry (P < 0.001). Among the 253 patients, the results showed that patients with low Cys-C expression level in cancer tissue has longer overall survival (OS) than that with high Cys-C level. Furthermore, knockout of Cys-C in 786-O cell line has ability to suppress cell proliferation, induce G0/G1 phase arrest, inhibited cell invasion, decreased phosphorylation of ERK1/2, STAT-3 and enhanced phosphorylated JNK expression. Conclusions: A decrease in serum Cys-C is a favorable prognostic indicator for CCRCC patients. Inhibition of CysC suppressed RCC 786-O cell proliferation and invasion. These results indicated that Cys-C could serve as an ideal prognostic biomarker in patients with CCRCC.
引用
收藏
页码:1237 / 1245
页数:9
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