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首页> 外文期刊>Reproductive Biology and Endocrinology >Enhanced expression of the stemness-related factors OCT4, SOX15 and TWIST1 in ectopic endometrium of endometriosis patients
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Enhanced expression of the stemness-related factors OCT4, SOX15 and TWIST1 in ectopic endometrium of endometriosis patients

机译:子宫内膜异位症患者异位内膜中干相关因子OCT4,SOX15和TWIST1的表达增强

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Background Current evidence suggests that endometrial-derived stem cells, spilled in the peritoneal cavity via retrograde menstruation, are key players in the establishment of endometriotic lesions. The aim of this study was to determine the presence and distribution of the stemness-related factors OCT4, SOX15, TWIST1 and DCAMLK1 in women with and without endometriosis. Methods Immunohistochemical analysis was used to determine stromal and epithelial expression of OCT4, SOX15, TWIST1 and DCAMLK1 in endometriosis patient (EP) endometrium ( n =?69) and endometriotic tissue ( n =?90) and in control endometrium ( n =?50). Quantitative Real-Time PCR of OCT4, SOX15 TWIST1 and DCAMLK1 was performed in paired samples of EP endometrium and endometriotic tissue. Co-immunofluorescence staining was performed for OCT4 and SOX15. For statistical analyses we used unpaired t -test, Fisher combination test and Spearman test. For paired analyses, paired t -test and McNemar test were used. Results We detected a significant correlation between the expression of the established stem cell marker OCT4 and the stemness-related markers SOX15 ( p Conclusion Our findings support the hypothesis that upregulation of stem cell-related factors contribute to the establishment of endometriotic lesions. Trial registration The study was approved by the institutional review board (545/2010?on 6th of May 2014) of the Medical University of Vienna ( http://ethikkommission.meduniwien.ac.at/fileadmin/ethik/media/dokumente/register/alle_2010.pdf ).
机译:背景技术目前的证据表明,子宫内膜来源的干细胞经月经逆行溢出到腹膜腔内,是子宫内膜异位病变形成的关键因素。这项研究的目的是确定在有或没有子宫内膜异位症的女性中,干性相关因子OCT4,SOX15,TWIST1和DCAMLK1的存在和分布。方法采用免疫组织化学方法检测子宫内膜异位症患者(EP)子宫内膜(n =?69)和子宫内膜异位组织(n =?90)和子宫内膜异位症(n =?50)中OCT4,SOX15,TWIST1和DCAMLK1的基质和上皮表达。 )。在EP子宫内膜和子宫内膜异位组织的配对样品中进行OCT4,SOX15 TWIST1和DCAMLK1的定量实时PCR。对OCT4和SOX15进行了共免疫荧光染色。对于统计分析,我们使用了不成对的t检验,Fisher组合检验和Spearman检验。对于配对分析,使用配对t检验和McNemar检验。结果我们检测到已建立的干细胞标志物OCT4的表达与干性相关标志物SOX15之间存在显着相关性(p结论)我们的发现支持以下假设:干细胞相关因子的上调有助于子宫内膜异位病变的建立。研究得到维也纳医科大学的机构审查委员会(545/2010?,2014年5月6日)批准(http://ethikkommission.meduniwien.ac.at/fileadmin/ethik/media/dokumente/register/alle_2010。 pdf)。

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