4.4 Article

Genistein Down-Regulates miR-223 Expression in Pancreatic Cancer Cells

期刊

CURRENT DRUG TARGETS
卷 14, 期 10, 页码 1150-1156

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/13894501113149990187

关键词

miR-223; Fbw7; apoptosis; cell growth; genistein; pancreatic cancer

资金

  1. NSFC [81172087]
  2. Natural Science Research key Project of Education Office of Anhui Province [KJ2012A196]

向作者/读者索取更多资源

Although genistein has been shown to inhibit tumorigenesis in a variety of human cancers including pancreatic cancer (PC), the exact molecular mechanism of its anti-cancer effects has not yet been fully elucidated. Recently, microRNAs (miRNAs) have been reported to regulate multiple aspects of tumor development and progression, indicating that targeting miRNAs could be a novel strategy to treat human cancers. In the current study, we investigated whether a natural compound genistein could down-regulate onco-miR-223, resulting in the inhibition of cell growth and invasion, and induction of apoptosis in PC cells. We found that genistein treatment significantly inhibited miR-223 expression and up-regulated Fbw7, one of the targets of miR-223. Moreover, down-regulation of miR-223 inhibited cell growth and induced apoptosis in PC cells. These findings suggest that genistein exerts its anti-tumor activity partly through downregulation of miR-223 in PC cells.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据