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

被引:189
作者
Guo, Li-Min
Pu, Yong
Han, Zhe
Liu, Tao
Li, Yi-Xuan
Liu, Min
Li, Xin
Tang, Hua [1 ,2 ]
机构
[1] Tianjin Med Univ, Tianjin Life Sci Res Ctr, Tianjin 300070, Peoples R China
[2] Tianjin Med Univ, Basic Med Sch, Tianjin 300070, Peoples R China
基金
中国国家自然科学基金;
关键词
cell growth; miR-9; NF-kappa B1; ovarian cancer; target gene; NF-KAPPA-B; SMALL RNAS; ADENOCARCINOMA; SPECIFICITY; MIRNAS; GENES; LET-7;
D O I
10.1111/j.1742-4658.2009.07237.x
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
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.
引用
收藏
页码:5537 / 5546
页数:10
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