4.6 Article

MicroRNA-9 inhibits ovarian cancer cell growth through regulation of NF-κB1

Journal

FEBS JOURNAL
Volume 276, Issue 19, Pages 5537-5546

Publisher

WILEY
DOI: 10.1111/j.1742-4658.2009.07237.x

Keywords

cell growth; miR-9; NF-kappa B1; ovarian cancer; target gene

Funding

  1. National Natural Science Foundation of China [30873017]
  2. Natural Science Foundation of Tianjin [08JCZDJC23300, 09JCZDJC17500]

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MicroRNAs are emerging as important regulators of cancer-related processes. Our studies show that microRNA-9 (miR-9) is downregulated in human ovarian cancer relative to normal ovary, and overexpression of miR-9 suppresses cell growth in vitro. Furthermore, the 3'-UTR of NF-kappa B1 mRNA is found to be regulated directly by miR-9, demonstrating that NF-kappa B1 is a functionally important target of miR-9 in ovarian cancer cells. When miR-9 is overexpressed in ovarian cancer cells, the mRNA and protein levels of NF-kappa B1 are both suppressed, whereas inhibition of miR-9 results in an increase in the NF-kappa B1 expression level. Ovarian cancer tissues display significantly low expression of miR-9 and a high level of NF-kappa B1 compared with normal tissues, indicating that regulation of NF-kappa B1 by miR-9 is an important mechanism for miR-9 to inhibit ovarian cancer proliferation.

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