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Differential expression and functional analysis of micro RNAs in emPapio anubis/em induced with endometriosis for early detection of the disease

机译:子宫内膜异位症诱导诱导的微rNA中微rnas的差异表达和功能分析,用于早期检测疾病

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Endometriosis is a common gynecological disorder affecting approximately 10% of women of reproductive age who often experience chronic pelvic pain and infertility. Laparoscopy, which is invasive and expensive, is the gold standard for diagnosis of endometriosis. A simple minimally-invasive test for endometriosis-specific biomarkers which is yet to be realized would offer a timely and accurate diagnosis for the disease thereby allowing early treatment intervention. Although aberrant microRNA expression has been implicated in endometriosis in several studies, conflicting results have been reported. This study hypothesized that the use of an appropriate animal model will provide a unique entry point for the discovery of biomarkers for early diagnosis of endometriosis. The study aimed at identifying miRNAs that are differentially expressed in eutopic endometrium of induced endometriosis in Papio anubis for early detection of endometriosis. Female adult baboons (n = 3) were induced with endometriosis by intraperitoneal inoculation of autologous menstrual endometrium. We sequenced small RNA samples obtained from normal (control) and diseased eutopic endometrium. Quality reads from the sequences were subjected to differential expression analysis using to identify dysregulated microRNAs and genes from other non-coding small RNA in the samples using a bioinformatics approach. Through in-silico analysis, gene targets of the dysregulated miRNA target genes and their functions were determined. Our findings show significant high expression of seven microRNAs namely miR-199a-3p, miR-145-5p, miR-214-3p, miR-143-3p, miR-125b-5p, miR-199a-5p and miR-10b-5p. The study also reveals five microRNAs that were significantly down regulated and they include miR-29b-3p, miR-16- 5p, miR-342-3p, miR-378a-3p and let-7g-5p. Seventeen genes from non-coding small RNAs were significantly dysregulated. The dysregulated microRNAs and genes play important roles in pathogenesis of endometriosis. Our findings indicate that specific miRNA signatures are associated with endometriosis, and the dysregulated miRNAs could constitute new and informative biomarkers for early diagnosis of endometriosis.
机译:子宫内膜异位症是一种常见的妇科疾病,影响了大约10%的生殖年龄妇女,常常经历慢性盆腔疼痛和不孕症。腹腔镜检查,侵入性和昂贵,是诊断子宫内膜异位症的金标准。对于尚待实现的子宫内膜异位症特异性生物标志物的一种简单的微创试验将为疾病提供及时和准确的诊断,从而允许早期治疗干预。虽然异常的microRNA表达在几项研究中涉及子宫内膜异位症,但报告了矛盾的结果。这项研究假设使用适当的动物模型的使用将为发现生物标志物的早期诊断提供了一个独特的进入点。该研究旨在鉴定MiRNA,其在诱导的子宫内膜异位症的诱导子宫内膜异位症中差异表达,用于早期检测子宫内膜异位症。通过腹腔接种自体月经内肿瘤内膜的子宫内膜异位症诱导女性成年狒狒(n = 3)。我们测序了从正常(对照)和患病的副肿瘤子宫内膜获得的小RNA样品。通过使用生物信息学方法鉴定来自样品中的其他非编码小RNA的鉴别的微小RNA和基因,对来自序列的质量读出差异表达分析。通过硅基分析,测定了失去的miRNA靶基因的基因靶标及其功能。我们的研究结果显示出七个MicroRNA的显着高表达,即MiR-199A-3P,MIR-145-5P,MIR-214-3P,MIR-143-3P,MIR-125B-5P,MIR-199A-5P和MIR-10B- 5P。该研究还揭示了5种MicroRNA,其显着调节,包括miR-29b-3p,miR-16-5p,miR-342-3p,miR-378a-3p和let-7g-5p。来自非编码小RNA的十七种基因显着失去了过量。失调的微小RNA和基因在子宫内膜异位症的发病机制中起重要作用。我们的研究结果表明,特定的miRNA签名与子宫内膜异位症有关,并且疑虑的miRNA可以构成新的和信息性的生物标志物,用于早期诊断子宫内膜异位症。

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