microRNA-342-5p and miR-608 inhibit colon cancer tumorigenesis by targeting NAA10

被引:67
|
作者
Yang, Hongju [1 ]
Li, Qian [2 ]
Niu, Jie [3 ]
Li, Bai [2 ]
Jiang, Dejun [1 ]
Wan, Zhihua [1 ]
Yang, Qingmei [1 ]
Jiang, Fei [1 ]
Wei, Ping [1 ]
Bai, Song [1 ]
机构
[1] Kunming Med Univ, Affiliated Hosp 1, Kunming, Yunnan, Peoples R China
[2] Yunnan Univ, Ctr Human Genet, Kunming, Yunnan, Peoples R China
[3] Chinese Acad Med Sci, Inst Med Biol, Kunming, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
NAA10; miR-342-5p; miR-608; colon cancer; POOR-PROGNOSIS; CELL-CYCLE; ARD1; PROTEIN; EXPRESSION; APOPTOSIS; LUNG;
D O I
10.18632/oncotarget.6458
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
miRNAs have been shown to play pivotal roles in the establishment and progression of colon cancer, but their underlying mechanisms are not fully understood. N-acetyltransferase NAA10 participates in many cellular processes, including tumorigenesis. Here we showed that miR-342-5p and miR-608 suppressed the tumorigenesis of colon cancer cells in vitro and in vivo by targeting NAA10 mRNA for degradation. Overexpression of miR-342-5p or miR-608 decreased NAA10 mRNA and protein levels and thereby suppressed cell proliferation, migration, and cell-cycle progression, as well as promoted apoptosis in SW480 and SW620 cells. More importantly, miR-342-5p and miR-608 significantly decreased the tumorigenic capacity of SW480 and SW620 cells in a mouse xenograft model. We also observed an inverse correlation between the expression of NAA10 and that of both miRNAs. Our results implicate miR-342-5p and miR-608 in colon cancer development and unveil the underlying mechanism of this phenomenon, which involves NAA10.
引用
收藏
页码:2709 / 2720
页数:12
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