miR-93/106b and Their Host Gene, MCM7, Are Differentially Expressed in Leiomyomas and Functionally Target F3 and IL-8

被引:91
作者
Chuang, Tsai-Der [1 ]
Luo, Xiaoping [1 ]
Panda, Harekrushna [1 ]
Chegini, Nasser [1 ]
机构
[1] Univ Florida, Dept Obstet & Gynecol, Gainesville, FL 32610 USA
基金
美国国家卫生研究院;
关键词
CATECHOL-O-METHYLTRANSFERASE; TISSUE FACTOR EXPRESSION; GROWTH-FACTOR; VASCULAR INFLAMMATION; UTERINE LEIOMYOMA; MICRORNA CLUSTER; HUMAN MYOMETRIUM; BREAST-CANCER; FACTOR VIIA; TGF-BETA;
D O I
10.1210/me.2012-1075
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
miR-93/106b and their host gene minichromosome maintenance complex component 7 (MCM7) reside at chr7q22, a region frequently rearranged in leiomyomas. We explored the expression of miR-93/106b in leiomyoma and paired myometrium (n = 63) from untreated and patients exposed to hormonal therapies (GnRH agonist, Depo-Provera, and oral contraceptives) from African-Americans and Caucasians and their regulatory functions in isolated paired (n = 15) leiomyoma and myometrial smooth muscle cells and the leiomyosarcoma cell line. At tissue level leiomyomas expressed significantly lower levels of miR-93 and elevated MCM7 as compared with myometrium with limited racial influence or hormonal exposure on their expression. Assessing the regulatory function of miR-93/106b through doxycycline-inducible lentiviral transduction in a microarray analysis, tissue factor (F3) and IL8 were identified as their possible targets. At the tissue level, leiomyomas expressed a significantly lower level of F3 and an elevated IL-8 level, which exhibited an inverse relationship with miR-93 but with limited racial or hormonal influences. The gain of function of miR-93/106b in leiomyoma smooth muscle cells, myometrial smooth muscle cells, and the leiomyosarcoma cell line dose dependently repressed F3 and IL8 through direct interactions with their respective 3'-untranslated region and indirectly through F3 repression inhibited IL8, CTGF, and PAI-1 expression, confirmed by using small interfering RNA silencing or factor VIIa (FVIIa) activation of F3, as well as reducing the rate of proliferation, while increasing caspase-3/7 activity. We concluded that differential expression of miR-93/106b and their direct and/or indirect regulatory functions on F3, IL8, CTGF, and PAI-1 expression, with key roles in inflammation and tissue turnover may be of significance in the outcome of leiomyoma growth and associated symptoms. (Molecular Endocrinology 26: 1028-1042, 2012)
引用
收藏
页码:1028 / 1042
页数:15
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