miR-21, miR-17 and miR-19a induced by phosphatase of regenerating liver-3 promote the proliferation and metastasis of colon cancer

被引:102
|
作者
Zhang, J. [1 ]
Xiao, Z. [1 ]
Lai, D.
Sun, J. [1 ]
He, C. [1 ]
Chu, Z.
Ye, H. [1 ]
Chen, S.
Wang, J. [1 ]
机构
[1] Sun Yat Sen Univ, Dept Hepatobiliary Surg, Sun Yat Sen Mem Hosp, Guangzhou 510120, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
PRL-3; microRNA; STAT3; colon carcinoma; PRL-3; PROMOTES; UP-REGULATION; GENE-EXPRESSION; GASTRIC-CANCER; STAT3; INVASION; MIGRATION; PROTEIN; GROWTH; CELLS;
D O I
10.1038/bjc.2012.251
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: Phosphatase of regenerating liver-3 (PRL-3) is an oncogene known to promote tumour metastasis, especially in colorectal cancer (CRC). Here, we demonstrate that the miR-21, miR-17 and miR-19a expressions induced by PRL-3 are involved in the proliferation and metastasis of colon cancer. METHODS: Microarray analysis and quantitative reverse-transcription polymerase chain reactions (qRT-PCR) were used to investigate the changes in miRNA expression due to the overexpression of PRL-3. Transwell chamber invasion assays, CCK-8 proliferation assays and RNA interference assays were used to explore the effects of PRL-3 on miR-21, miR-17 and miR-19a expression in colon cancer cells. Immunohistochemistry and qRT-PCR were performed in colon cancer tissues to evaluate the expression of PRL-3, signal transducer and activator of transcription 3 (STAT3), miR-21, miR-17 and miR-19a. RESULTS: Our study demonstrated that the overexpression of PRL-3 in colon cancer cells induced the expression of miR-21, miR-17 and miR-19a by activating STAT3. Subsequently, these microRNAs contributed to the increased proliferation and invasiveness of the colon cancer cells. Positive correlations between PRL-3 and these microRNAs were also observed in matched primary colon cancer tissues and metastatic lesions. CONCLUSION: miR-21, miR-17 and miR-19a induced by PRL-3 contribute to the proliferation and invasion of colon cancer. British Journal of Cancer (2012) 107, 352-359. doi:10.1038/bjc.2012.251 www.bjcancer.com Published online 7 June 2012 (c) 2012 Cancer Research UK
引用
收藏
页码:352 / 359
页数:8
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