The effect of raloxifene, a SERM, on extracellular matrix protein expression of pelvic fibroblasts

被引:2
|
作者
Lee, Jung Han [2 ]
Wen, Yan [1 ]
Polan, Mary Lake [1 ]
Chen, Bertha [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Obstet & Gynecol, Stanford, CA 94305 USA
[2] Hanyang Univ, Sch Med, Dept Obstet & Gynecol, Seoul 133791, South Korea
基金
美国国家卫生研究院;
关键词
Collagen; MMP; Pelvic organ prolapse; Raloxifene; TIMP; Pelvic floor disorder; ESTROGEN-RECEPTOR MODULATORS; STRESS URINARY-INCONTINENCE; BETA MESSENGER RNA; ORGAN PROLAPSE; POSTMENOPAUSAL WOMEN; COLLAGEN-METABOLISM; VAGINAL TISSUE; ISOFORM-ALPHA; INHIBITORS; CELLS;
D O I
10.1007/s00192-011-1567-0
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
We hypothesize that the abnormal extracellular matrix (ECM) turnover in pelvic tissues of women with prolapse may be attenuated by raloxifene. We examine the effect of raloxifene on ECM protein expression in pelvic fibroblasts. Pelvic fibroblasts were isolated from cases (N = 6) and controls (N = 3). Cells were treated with raloxifene. Dose-response analyses were performed by ANOVA. mRNA and protein expression of collagen I, III, MMPs, and TIMPs were determined by RT-PCR and Western blot. MMP activity was analyzed by zymography. The mRNA expression of TIMP-3 and protein expression of TIMP-1 and TIMP-3 were significantly increased by raloxifene in fibroblasts from both cases and controls (P < 0.05). Collagen I, III, and MMP mRNA and protein expressions were not affected. Raloxifene selectively attenuates abnormal matrix degradation by increasing inhibitors of proteases, TIMPs, in pelvic fibroblasts. This opens the possibility for SERMs to be used as preventive therapy for pelvic floor disorders.
引用
收藏
页码:349 / 355
页数:7
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