MiR-143 inhibits cell proliferation and invasion by targeting DNMT3A in gastric cancer

被引:28
|
作者
Zhang, Quan [1 ,2 ]
Feng, Yong [1 ,3 ]
Liu, Ping [1 ]
Yang, Jing [4 ]
机构
[1] Nanjing Med Univ, Affiliated Hosp 1, Dept Oncol, Nanjing 210029, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Huaian Peoples Hosp 1, Dept Radiat Oncol, Huaian, Peoples R China
[3] Nanjing Med Univ, Huaian Peoples Hosp 1, Dept Oncol, Huaian, Peoples R China
[4] Nanjing Med Univ, Huaian Peoples Hosp 1, Dept Cardiol, 6 Beijing West Rd, Huaian 223300, Peoples R China
关键词
Gastric cancer; miR-143; DNMT3A; cell proliferation; cell invasion; TUMOR-SUPPRESSOR; EXPRESSION; MICRORNA-143; MORTALITY;
D O I
10.1177/1010428317711312
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Increasing evidence has suggested that MircroRNAs (miRNAs) dysregulated in pathogenesis and tumorigenicity in human cancers including gastric cancer (GC). MiR-143 had been reported to function as tumor suppressor in GC progression, however, the underlying function of miR-143 in GC still need to be well known. In the study, we revealed that miR-143 was significantly down-regulated in GC cell lines. Upregulation of miR-143 inhibited cell proliferation, invasion, S phase cell proportion and cell cycle related protein levels of Cyclin D1, CDK4 and CDK6 in GC. Furthermore, luciferase reporter assays demonstrated that DNMT3A was a direct target of miR-143 and Upregulation of miR-143 inhibited the DNMT3A mRNA and protein expression levels in GC cells. Moreover, we demonstrated that DNMT3A knockdown rescued the promoting effect of miR-143 inhibitor on cell proliferation in GC. Thus, these results demonstrated that miR-143 targeted DNMT3A in GC cells and inhibit GC tumorigenesis and progression, which may provide a novel therapeutic target of GC.
引用
收藏
页码:1 / 8
页数:8
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