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2000
Volume 14, Issue 10
  • ISSN: 1389-4501
  • E-ISSN: 1873-5592

Abstract

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.

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/content/journals/cdt/10.2174/13894501113149990187
2013-09-01
2025-05-23
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/content/journals/cdt/10.2174/13894501113149990187
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  • Article Type:
    Research Article
Keyword(s): apoptosis; cell growth; Fbw7; genistein; miR-223; pancreatic cancer
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