Department of Obstetrics, Gynecology, and Reproductive Sciences, University of California, San Francisco, 505 Parnassus Avenue, San Francisco, California 94143-0132, USA.
J Clin Endocrinol Metab. 2013 Sep;98(9):3765-75. doi: 10.1210/jc.2013-1923. Epub 2013 Jul 3.
Endometrium in polycystic ovary syndrome (PCOS) presents altered gene expression indicating progesterone resistance and predisposing to reduced endometrial receptivity and endometrial cancer.
We hypothesized that an altered endocrine/metabolic environment in PCOS may result in an endometrial "disease phenotype" affecting the gene expression of different endometrial cell populations, including stem cells and their differentiated progeny.
This was a prospective study conducted at an academic medical center.
Proliferative-phase endometrium was obtained from 6 overweight/obese PCOS (National Institutes of Health criteria) and 6 overweight/obese controls. Microarray analysis was performed on fluorescence-activated cell sorting-isolated endometrial epithelial cells (eEPs), endothelial cells, stromal fibroblasts (eSFs), and mesenchymal stem cells (eMSCs). Gene expression data were validated using microfluidic quantitative RT-PCR and immunohistochemistry.
The comparison between eEP(PCOS) and eEP(Ctrl) showed dysregulation of inflammatory genes and genes with oncogenic potential (CCL2, IL-6, ORM1, TNAIFP6, SFRP4, SPARC). eSF(PCOS) and eSF(Ctrl) showed up-regulation of inflammatory genes (C4A/B, CCL2, ICAM1, TNFAIP3). Similarly, in eMSC(PCOS) vs eMSC(Ctrl), the most up-regulated genes were related to inflammation and cancer (IL-8, ICAM1, SPRR3, LCN2). Immunohistochemistry scoring showed increased expression of CCL2 in eEP(PCOS) and eSF(PCOS) compared with eEP(Ctrl) and eSF(Ctrl) and IL-6 in eEP(PCOS) compared with eEP(Ctrl).
Isolated endometrial cell populations in women with PCOS showed altered gene expression revealing inflammation and prooncogenic changes, independent of body mass index, especially in eEP(PCOS) and eMSC(PCOS), compared with controls. The study reveals an endometrial disease phenotype in women with PCOS with potential negative effects on endometrial function and long-term health.
多囊卵巢综合征(PCOS)的子宫内膜表现出改变的基因表达,表明孕激素抵抗,并易发生子宫内膜容受性降低和子宫内膜癌。
我们假设 PCOS 中改变的内分泌/代谢环境可能导致子宫内膜“疾病表型”,影响不同子宫内膜细胞群体的基因表达,包括干细胞及其分化后代。
这是在学术医疗中心进行的前瞻性研究。
从 6 名超重/肥胖的 PCOS 患者(美国国立卫生研究院标准)和 6 名超重/肥胖的对照者中获得增生期子宫内膜。对荧光激活细胞分选分离的子宫内膜上皮细胞(eEPs)、内皮细胞、基质成纤维细胞(eSFs)和间充质干细胞(eMSCs)进行微阵列分析。使用微流控定量 RT-PCR 和免疫组织化学验证基因表达数据。
eEP(PCOS)与 eEP(Ctrl)的比较显示,炎症基因和具有致癌潜力的基因(CCL2、IL-6、ORM1、TNAIFP6、SFRP4、SPARC)失调。eSF(PCOS)和 eSF(Ctrl)显示炎症基因(C4A/B、CCL2、ICAM1、TNFAIP3)上调。同样,在 eMSC(PCOS)与 eMSC(Ctrl)相比,上调最明显的基因与炎症和癌症有关(IL-8、ICAM1、SPRR3、LCN2)。免疫组织化学评分显示,与 eEP(Ctrl)和 eSF(Ctrl)相比,eEP(PCOS)和 eSF(PCOS)中 CCL2 的表达增加,eEP(PCOS)中 IL-6 的表达增加。
与对照组相比,PCOS 妇女的分离子宫内膜细胞群表现出改变的基因表达,显示出炎症和促癌变化,这与体重指数无关,尤其是在 eEP(PCOS)和 eMSC(PCOS)中。该研究揭示了 PCOS 妇女的子宫内膜疾病表型,可能对子宫内膜功能和长期健康产生负面影响。