miR-20a promotes proliferation and invasion by targeting APP in human ovarian cancer cells

被引:90
作者
Fan, Xingxing
Liu, Yankun
Jiang, Jiechun
Ma, Zhuoya
Wu, Haidong
Liu, Tao
Liu, Min
Li, Xin
Tang, Hua [1 ]
机构
[1] Tianjin Med Univ, Tianjin Life Sci Res Ctr, Tianjin 300070, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-20a; ovarian carcinoma; colony formation; invasion; amyloid precursor protein (APP); AMYLOID PRECURSOR PROTEIN; EXPRESSION; MICRORNAS; DEREGULATION; MIR-17-92; GENE;
D O I
10.1093/abbs/gmq026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
MicroRNAs (miRNAs) are emerging as a class of small regulated RNAs, and the alterations of miRNAs are implicated in the initiation and progression of human cancers. Our study shows that inhibition of miR-20a in OVCAR3 ovarian cancer cell line could suppress, whereas overexpression of miR-20a could enhance cell long- term proliferation and invasion. We also confirmed amyloid precursor protein (APP) as a direct target gene of miR20a. Furthermore, suppression of APP expression could also promote ovarian cancer cell proliferation and invasion, which is consistent with the results of miR-20a overexpression. Therefore, we concluded that the regulation of APP is an important mechanism for miR-20a to promote proliferation and invasion in ovarian cancer cells.
引用
收藏
页码:318 / 324
页数:7
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