首页> 外文期刊>Fertility and Sterility: Official Journal of the American Fertility Society, Pacific Coast Fertility Society, and the Canadian Fertility and Andrology Society >Prokineticin 1, homeobox A10, and progesterone receptor messenger ribonucleic acid expression in primary cultures of endometrial stromal cells isolated from endometrium of healthy women and from eutopic endometrium of women with endometriosis.
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Prokineticin 1, homeobox A10, and progesterone receptor messenger ribonucleic acid expression in primary cultures of endometrial stromal cells isolated from endometrium of healthy women and from eutopic endometrium of women with endometriosis.

机译:从健康妇女的子宫内膜和子宫内膜异位症妇女的子宫内膜分离的子宫内膜基质细胞原代培养物中,促动蛋白1,同源盒A10和孕激素受体信使核糖核酸的表达。

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OBJECTIVE: To examine prokineticin 1 (PROK1), homeobox (HOX) A10, and P receptor (PR) messenger ribonucleic acid (mRNA) expression in primary cultures of endometrial stromal cells (ESC) obtained from eutopic endometrial samples of patients with endometriosis and to clarify whether in vitro steroid hormone dependence of PROK1 gene expression is altered in endometriosis. DESIGN: Prospective laboratory study. SETTING: Tertiary university hospital. PATIENT(S): Twelve normal women (controls) and 12 patients affected by moderate to severe endometriosis in the midsecretory phase of the menstrual cycle. INTERVENTION(S): Endometrial specimens were obtained from control women and from women affected by endometriosis; ESC were isolated from endometrial biopsies, and primary cultures were established. MAIN OUTCOME MEASURE(S): Real-time polymerase chain reaction analysis of PROK1, HOXA10, and PR mRNA expression in ESC after 1-4 days of steroid hormone treatment and after decidual differentiation. RESULT(S): Contrary to ESC from control women, in ESC obtained from women affected by endometriosis PROK1 and PR mRNA expression was not induced by 1-4 days of treatment with steroid hormones. Nevertheless, when ESC from both groups of women were differentiated to decidual phenotype, PROK1 mRNA was up-regulated and PR and HOXA10 mRNA were down-regulated to the same extent. CONCLUSION(S): Our results provide additional evidence for P resistance in endometriosis.
机译:目的:研究从原位子宫内膜异位症患者的子宫内膜基质细胞(ESC)的原代培养物中子宫内膜基质细胞(ESC)的原动蛋白1(PROK1),同源盒(HOX)A10和P受体(PR)信使核糖核酸(mRNA)的表达。阐明子宫内膜异位症中PROK1基因表达的体外类固醇激素依赖性是否改变。设计:前瞻性实验室研究。地点:大专医院。患者:十二名正常妇女(对照组)和十二名患者在月经周期的分泌中期受到中度至重度子宫内膜异位症的影响。干预措施:子宫内膜标本取自对照妇女和受子宫内膜异位症影响的妇女。从子宫内膜活组织检查中分离出ESC,并建立了原代培养物。主要观察指标:类固醇激素治疗1-4天后和蜕膜分化后,ESC中PROK1,HOXA10和PR mRNA表达的实时聚合酶链反应分析。结果:与对照女性的ESC相反,在接受子宫内膜异位症PROK1和PR mRNA表达影响的女性获得的ESC中,类固醇激素治疗1-4天未诱发。但是,当两组女性的ESC分化为蜕膜表型时,PROK1 mRNA均被上调,PR和HOXA10 mRNA均被下调至相同程度。结论:我们的结果为子宫内膜异位症的P抵抗提供了更多证据。

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