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选择性孕激素受体调节剂对体内子宫肌瘤细胞凋亡诱导作用的影响。

Effect of a selective progesterone receptor modulator on induction of apoptosis in uterine fibroids in vivo.

机构信息

Department of Obstetrics and Gynaecology, First Faculty of Medicine, Charles University in Prague, Apolinarska 18, 128 00 Prague, Czech Republic.

出版信息

Int J Endocrinol. 2012;2012:436174. doi: 10.1155/2012/436174. Epub 2012 Jul 16.

Abstract

Aim. To determine if hormonal treatment induces apoptosis in uterine fibroids. Methods. Immunohistochemical examination of fibroid tissue, using avidin-biotin complex and cleaved caspase-3 antibody for detecting apoptosis, was performed in premenopausal women who underwent 12-week treatment with oral SPRM (6 patients with 5 mg and 5 patients with 10 mg of ulipristal acetate per day) or gonadoliberin agonist (GnRHa, 17 patients) and subsequent myomectomy or hysterectomy for symptomatic uterine fibroids. Ten patients with no presurgical hormonal treatment were used as controls. Results. Apoptosis was present in a significantly higher proportion of patients treated with ulipristal acetate compared to GnRHa (P = 0.01) and to patients with no hormonal treatment (P = 0.01). In contrast to an AI of 158.9 in SPRM patients, the mean AI was 27.5 and 2.0 in GnRHa and control groups, respectively. No statistical difference in the AI was observed between the two groups of patients treated with ulipristal acetate (5 mg or 10 mg). Conclusion. Treatment with ulipristal acetate induces apoptosis in uterine fibroid cells. This effect of SPRM may contribute to their positive clinical effect on uterine fibroids.

摘要

目的。确定激素治疗是否会诱导子宫肌瘤细胞凋亡。方法。对接受为期 12 周的口服 SPRM(每天 5mg 和 10mg 醋酸乌利司他 6 例和 5 例)或促性腺激素释放激素激动剂(GnRHa,17 例)治疗的绝经前妇女的子宫肌瘤组织进行免疫组织化学检查,使用亲和素-生物素复合物和裂解的半胱天冬酶-3 抗体检测凋亡。因有症状的子宫肌瘤而行子宫肌瘤切除术或子宫切除术。将 10 例无术前激素治疗的患者作为对照组。结果。与 GnRHa(P=0.01)和无激素治疗的患者(P=0.01)相比,接受醋酸乌利司他治疗的患者中凋亡的比例明显更高。与 SPRM 患者的平均 AI 为 158.9 相比,GnRHa 和对照组的平均 AI 分别为 27.5 和 2.0。接受醋酸乌利司他治疗的两组患者的 AI 无统计学差异(5mg 或 10mg)。结论。醋酸乌利司他治疗可诱导子宫肌瘤细胞凋亡。SPRM 的这种作用可能有助于其对子宫肌瘤的积极临床疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3213/3403220/6f9e748a986a/IJE2012-436174.001.jpg

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