Long non-coding RNA PlncRNA-1 promotes cell proliferation and hepatic metastasis in colorectal cancer

被引:24
作者
Jia, Gui-Qing [1 ,2 ,3 ,4 ]
Zhang, Ming-Ming [5 ]
Wang, Kang [3 ,4 ]
Zhao, Gao-Ping [3 ,4 ]
Pang, Ming-Hui [3 ,4 ]
Chen, Zhe-Yu [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Liver Surg, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Liver Transplantat Ctr, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Acad Med Sci, Dept Gastrointestinal Surg, Chengdu, Peoples R China
[4] Sichuan Prov Peoples Hosp, Chengdu, Sichuan, Peoples R China
[5] Sichuan Univ, West China Hosp, Dept Gastrointestinal Surg, Chengdu, Sichuan, Peoples R China
关键词
CRC; miR-204; MMP9; PlncRNA-1; Wnt; -catenin; EPITHELIAL-MESENCHYMAL TRANSITION; UP-REGULATION; CERNA; PROGRESSION; EXPRESSION; MICRORNAS; APOPTOSIS; INVASION; AXIS;
D O I
10.1002/jcb.27031
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Emerging evidence has identified that long non-coding RNAs (lncRNAs) may play an important role in the pathogenesis of many cancer types, including colorectal cancer (CRC). However, the role of PlncRNA-1 in CRC remains unclear. The aim of our present study was to investigate the potential functions of PlncRNA-1 in CRC and to identify the underlying mechanisms of action. We demonstrated that up-regulated PlncRNA-1 in CRC tissues and cells promoted cell proliferation by accelerating cell cycle process and inhibiting cell apoptosis in vitro, enhanced tumor growth and matastasis in vivo and was associated with cell migration and invasion, EMT process of CRC cells. In addition, PlncRNA-1 was a target of miR-204 and enhanced the expression of an endogenous miR-204 target, MMP9 in CRC cells. Furthermore, we found that PlncRNA-1 activates Wnt/-catenin pathway through the miR-204 in CRC cells. These results suggest that the PlncRNA-1/miR-204/ Wnt/-catenin regulatory network may shed light on tumorigenesis in CRC.
引用
收藏
页码:7091 / 7104
页数:14
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