Downregulated long non-coding RNA CLMAT3 promotes the proliferation of colorectal cancer cells by targeting regulators of the cell cycle pathway

被引:20
作者
Ye, Le-chi [1 ,2 ]
Chen, Tao [1 ]
Zhu, De-xiang [1 ]
Lv, Shi-xu [1 ]
Qiu, Jun-jun [3 ]
Xu, Jianmin [1 ]
Yuan, Feng-lai [4 ]
Wei, Ye [1 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Gen Surg, Shanghai, Peoples R China
[2] Wenzhou Med Univ, Dept Surg Oncol, Affiliated Hosp 1, Wenzhou, Peoples R China
[3] Fudan Univ, Dept Gynecol, Obstet & Gynecol Hosp, Shanghai, Peoples R China
[4] Nantong Univ, Hosp Affiliated 3, Nantong, Peoples R China
关键词
colorectal cancer; long non-coding RNA; lncRNA-CLMAT3; cell cycle pathway; EXPRESSION;
D O I
10.18632/oncotarget.10431
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Over-expression of long non-coding RNA (lncRNA)-CLMAT3 is significantly associated with colorectal liver metastasis and is an independent predictor of poor survival for colorectal cancer patients. However, as little is known regarding the role of this gene in the proliferation of colorectal cancer in vitro, we investigated the involvement of lncRNA-CLMAT3 in colorectal cancer cell proliferation. In this study, we demonstrate that lncRNA-CLMAT3 expression was significantly increased in colorectal cancer cells compared with a normal intestinal mucous cell line and that inhibition of lncRNA-CLMAT3 suppressed colorectal cancer cell proliferation in vitro. We also found that this reduced colorectal cancer cell proliferation due to lncRNA-CLMAT3 knockdown is associated with G0/G1 cell-cycle arrest induction and apoptosis enhancement. Furthermore, lncRNA-CLMAT3 knockdown enhanced Cdh1 expression and resulted in p27Kip accumulation via increased Skp2 protein ubiquitination. Taken together, our findings suggest that reducing lncRNA-CLMAT3 inhibits colorectal cancer cell proliferation by affecting cell cycle components.
引用
收藏
页码:58931 / 58938
页数:8
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