microRNA-199a:子宫内膜异位症中的关键因子
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  • 英文篇名:microRNA-199a:a key factor in endometriosis
  • 作者:苟凤钗 ; 杨红 ; 钱麟 ; 章晓乐 ; 齐聪
  • 英文作者:GOU Fengchai;YANG Hong;QIAN Lin;Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine;
  • 关键词:子宫内膜异位症 ; miR-199a ; 核因子-κB ; 白细胞介素-8 ; 血管内皮生长因子A
  • 英文关键词:endometriosis;;miR-199a;;nuclear factor-κB;;interleukin-8;;vascular endothelial growth factor A
  • 中文刊名:HBYZ
  • 英文刊名:Hebei Medical Journal
  • 机构:上海中医药大学附属曙光医院妇科;
  • 出版日期:2019-06-26
  • 出版单位:河北医药
  • 年:2019
  • 期:v.41
  • 基金:上海中医药大学名老中医药专家经验研究项目(SZYMZYGZS4014);上海中医药大学预算内项目(编号:2016YSN43);; 国家自然科学基金青年项目(编号:81704108)
  • 语种:中文;
  • 页:HBYZ201912033
  • 页数:6
  • CN:12
  • ISSN:13-1090/R
  • 分类号:130-135
摘要
子宫内膜异位症是一种常见的雌激素依赖性疾病,其特征在于子宫外的子宫内膜组织的生长。微小RNA最近已被确定为调节靶基因表达的调节因子,并被认为参与子宫内膜异位症的发展。miR-199a在子宫内膜异位症患者子宫内膜中的表达水平较低,与正常女性子宫内膜相比,卵巢子宫内膜瘤的表达水平甚至更低。MiR-199a在子宫内膜间质细胞(ESC)中靶向并抑制IkappaB激酶β(IKKb),随着IKKb的减少,miR-199a抑制了ESC中的核因子-κB(NF-κB)途径激活和白细胞介素-8(IL-8)的产生。miR-199a通过血管内皮生长因子A(VEGF-A)途径抑制部分缺氧条件下胚胎干细胞的血管生成潜能。所有这些发现表明,在子宫内膜异位症中下调的miR-199a部分通过IKK/NF-κB途径,VEGF-A途径抑制和降低的IL-8表达减弱了体外胚胎干细胞的粘附侵袭和血管生成能力。因此,miR-199a可能在子宫内膜异位症的发病机制中发挥关键作用,并可能成为该疾病的潜在治疗靶点。
        Endometriosis is a common estrogen-dependent disorder characterized by the growth of endometrial tissue outside the uterus.MicroRNAs have recently been identified as regulators of target gene expression and are thought to be involved in the development and progression of endometriosis.In patients with endometriosis,the expression levels of miR-199a in the endometrium in situ are low,and the expression levels of ovarian endometrioma are even lower than those in normal female endometrium.MiR-199a targets and inhibits IkappaB kinase(IKKb) in endometrial stromal cells(ESC).With the decrease of IKKb,miR-199a inhibits the nuclear factor-κB(NF-κB) pathway activation and the production of interleukin-8(IL-8) in ESC.Moreover Mir-199a inhibits the angiogenic potential of embryonic stem cells under partial hypoxia through the vascular endothelial growth factor A(VEGF-A) pathway.All these findings suggest that the down-regulated miR-199a portion of endometriosis reduces the adhesion invasion and angiogenesis of embryonic stem cells in vitro by inhibiting and decreasing IL-8 expression through the IKK/NF-κB pathway and VEGF-A pathway.Therefore,miA-199a may play a key role in the pathogenesis of endometriosis and may be a potential therapeutic target for this disease.
引文
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