Gao Shan, Liu Shuang, Gao Zi-Ming, Deng Peng, Wang Dan-Bo
Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang 110042, Liaoning Province, China.
Department of Surgical Oncology and General Surgery, First Affiliated Hospital of China Medical University, Shenyang 110042, Liaoning Province, China.
World J Clin Cases. 2019 Aug 26;7(16):2155-2164. doi: 10.12998/wjcc.v7.i16.2155.
Endometriosis (EMs) is a chronic and recurrent, but benign, disease in women of reproductive age, and EMs patients have a high risk of developing gynecological tumors and autoimmune disorders. The etiology of EMs is not clear. Certain genetic markers in the eutopic endometrium are key in the pathogenesis of EMs. MicroRNAs (miRNAs) are implicated in several biological processes, such as cell proliferation, differentiation, and apoptosis. MiR-451 is interesting, as it acts as a tumor suppressor and is relevant to the poor prognosis of cancers.
To evaluate the expression levels and role of miR-451 in the eutopic endometrium and predict possible targets of miR-451 and related signaling pathways.
Quantitative real-time polymerase chain reaction was used to evaluate miR-451 expression in cultured cell lines as well as in pathologic tissues from 40 patients with EMs and 20 donors with no history of the disease (controls). Cell Counting Kit-8 and flow cytometric assays were performed to determine cell proliferation and survival rates after transfection with miR-451 mimics and siRNAs. MiR-451 targets were predicted using miRDB and miRcode target-predicting databases.
We observed lower miR-451 levels in eutopic endometrial tissues from patients with EMs than in control tissues, and this difference was not related to the American Society for Reproductive Medicine stage. Ectopic overexpression of miR-451 in eutopic cells induced apoptosis and inhibited cell proliferation. SiRNA-mediated miR-451 knockdown reversed these effects. Using miRDB and miRcode, we identified 12 potential miR-451 target genes. We hypothesize that the expression of , , , and may be regulated by miR-451 and be involved in disease pathogenesis.
Reduced miR-451 expression in the eutopic endometrium contributes to the pathogenesis of EMs by promoting cell proliferation and reducing apoptosis. Thus, miR-451 is a novel biomarker for EMs. , , , and are potential target genes of miR-451 and may have key roles in this disease.
子宫内膜异位症(EMs)是一种发生于育龄女性的慢性复发性良性疾病,EMs患者发生妇科肿瘤和自身免疫性疾病的风险较高。EMs的病因尚不清楚。在位内膜中的某些遗传标志物是EMs发病机制的关键。微小RNA(miRNAs)参与多种生物学过程,如细胞增殖、分化和凋亡。MiR-451很有趣,因为它作为一种肿瘤抑制因子,与癌症的不良预后相关。
评估miR-451在位内膜中的表达水平和作用,并预测miR-451可能的靶标及相关信号通路。
采用定量实时聚合酶链反应评估miR-451在培养细胞系以及40例EMs患者和20例无该病病史的供体(对照)的病理组织中的表达。转染miR-451模拟物和小干扰RNA后,进行细胞计数试剂盒-8检测和流式细胞术检测以确定细胞增殖和存活率。使用miRDB和miRcode靶标预测数据库预测miR-451的靶标。
我们观察到EMs患者在位内膜组织中的miR-451水平低于对照组织,且这种差异与美国生殖医学学会分期无关。在位细胞中miR-451的异位过表达诱导细胞凋亡并抑制细胞增殖。小干扰RNA介导的miR-451敲低逆转了这些效应。使用miRDB和miRcode,我们鉴定出12个潜在的miR-451靶基因。我们推测, 、 、 和 的表达可能受miR-451调控,并参与疾病发病机制。
在位内膜中miR-451表达降低通过促进细胞增殖和减少细胞凋亡而促进EMs的发病机制。因此,miR-451是EMs的一种新型生物标志物。 、 、 和 是miR-451的潜在靶基因,可能在该疾病中起关键作用。