Upregulation of MicroRNA-107 induces proliferation in human gastric cancer cells by targeting the transcription factor FOXO1

被引:51
作者
Li, Fan [1 ]
Liu, Baohua [1 ]
Gao, Yu [1 ]
Liu, Yuliang [2 ]
Xu, Yu [3 ]
Tong, Weidong [1 ]
Zhang, Anping [1 ]
机构
[1] Third Mil Med Univ, Daping Hosp, Inst Surg Res, Dept Gen Surg, Chongqing 400042, Peoples R China
[2] Chongqing Med Univ, Affiliated Hosp 1, Dept Resp Med, Chongqing 400016, Peoples R China
[3] Third Mil Med Univ, Xinqiao Hosp, Inst Resp Dis, Chongqing 400037, Peoples R China
基金
中国国家自然科学基金;
关键词
MicroRNA-107; FOXO1; Gastric cancer; Cell proliferation; CONSTITUTIVE PHOSPHORYLATION; TUMOR-SUPPRESSOR; PROGRESSION; EXPRESSION; ANGIOGENESIS; CARCINOMA; DICER1;
D O I
10.1016/j.febslet.2013.12.009
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
MicroRNA-107 (miR-107) has been demonstrated to regulate proliferation and apoptosis in many types of cancers. Nevertheless, its biological function in gastric cancer remains largely unexplored. Here, we found that the expression level of miR-107 was increased in gastric cancer in comparison with the adjacent normal tissues. The enforced expression of miR-107 was able to promote cell proliferation in NCI-N87 and AGS cells, while miR-107 antisense oligonucleotides (antisense miR-107) blocked cell proliferation. At the molecular level, our results further revealed that expression of FOXO1 was negatively regulated by miR-107. Therefore, the data reported here demonstrate that miR-107 is an important regulator in gastric cancer, which will contribute to a better understanding of the important mis-regulated miRNAs in gastric cancer. (C) 2014 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:538 / 544
页数:7
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