Queensland Institute of Medical Research, Herston, Brisbane, Queensland, Australia.
Mol Hum Reprod. 2011 Feb;17(2):92-103. doi: 10.1093/molehr/gaq084. Epub 2010 Oct 8.
Previous microarray analyses identified 22 microRNAs (miRNAs) differentially expressed in paired ectopic and eutopic endometrium of women with and without endometriosis. To investigate further the role of these miRNAs in women with endometriosis, we conducted an association study aiming to explore the relationship between endometriosis risk and single-nucleotide polymorphisms (SNPs) in miRNA target sites for these differentially expressed miRNAs. A panel of 102 SNPs in the predicted miRNA binding sites were evaluated for an endometriosis association study and an ingenuity pathway analysis was performed. Fourteen rare variants were identified in this study. We found SNP rs14647 in the Wolf-Hirschhorn syndrome candidate gene1 (WHSC1) 3'UTR (untranslated region) was associated with endometriosis-related infertility presenting an odds ratio of 12.2 (95% confidence interval = 2.4-60.7, P = 9.03 × 10(-5)). SNP haplotype AGG in the solute carrier family 22, member 23 (SLC22A23) 3'UTR was associated with endometriosis-related infertility and more severe disease. With the individual genotyping data, ingenuity pathways analysis identified the tumour necrosis factor and cyclin-dependant kinase inhibitor as major factors in the molecular pathways. Significant associations between WHSC1 alleles and endometriosis-related infertility and SLC22A23 haplotypes and the disease severe stage were identified. These findings may help focus future research on subphenotypes of this disease. Replication studies in independent large sample sets to confirm and characterize the involvement of the gene variation in the pathogenesis of endometriosis are needed.
先前的微阵列分析鉴定了在患有和不患有子宫内膜异位症的女性的异位和正常子宫内膜中差异表达的 22 个 microRNAs(miRNAs)。为了进一步研究这些 miRNAs 在子宫内膜异位症患者中的作用,我们进行了一项关联研究,旨在探索这些差异表达 miRNA 的 miRNA 靶位的单核苷酸多态性(SNP)与子宫内膜异位症风险之间的关系。在 miRNA 结合位点预测中评估了一组 102 个 SNP,进行了 ingenuity 通路分析。在这项研究中发现了 14 种罕见变异。我们发现 Wolf-Hirschhorn 综合征候选基因 1(WHSC1)3'UTR(非翻译区)中的 SNP rs14647 与子宫内膜异位症相关的不孕不育有关,其比值比为 12.2(95%置信区间为 2.4-60.7,P = 9.03×10(-5))。溶质载体家族 22 成员 23(SLC22A23)3'UTR 中的 SNP 单体型 AGG 与子宫内膜异位症相关的不孕不育和更严重的疾病有关。利用个体基因分型数据,ingenuity 通路分析确定肿瘤坏死因子和细胞周期依赖性激酶抑制剂为分子通路中的主要因素。WHSC1 等位基因与子宫内膜异位症相关的不孕不育以及 SLC22A23 单体型与疾病严重程度之间存在显著关联。这些发现可能有助于将未来的研究集中在该疾病的亚表型上。需要在独立的大样本集中进行复制研究,以确认和描述基因变异在子宫内膜异位症发病机制中的作用。