子宫内膜异位症疾病通路相关基因的生物信息学富集分析

Kushum Kusum, Ashish Ashish, Ravi Bhushan, Radha Chaube, Sangeeta Rai, Royana Singh
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摘要

子宫内膜异位症是一种妇科疾病,子宫(异位)内膜腺体和组织存在于子宫内位置、异位区域(盆腔腹膜、输卵管或卵巢)之外。约有 5-10%的育龄妇女和 20-50% 的不孕妇女患有子宫内膜异位症。子宫内膜异位症的发病机制与多种因素有关,如激素、环境、遗传和免疫系统等,这些因素直接或间接地改变了雌激素水平,从而影响了妇女的生殖健康。目前的研究旨在利用 mRNA seq 分析找出子宫内膜异位症潜在的新型生物标记物。研究人员从原始基因表达谱中发现了差异表达基因(DEGs),并进一步对其进行了功能分析。与对照组相比,在患有子宫内膜异位症的妇女样本中总共发现了 552 个 DEGs(312 个上调,240 个下调)。发现形成枢纽节点的主要 DEGs(如 C3、PSAP、APP、GNG12)参与了上皮细胞分化和发育、蛋白分解、腺体发育、肌纤维发育、对激素刺激的反应等多种功能。所发现的 DEGs 可直接或间接参与子宫内膜异位症的发病机制,并可作为异位子宫内膜的潜在生物标志物。目前的研究将为子宫内膜异位症的发病机制提供一个初步的认识,但其完整的作用路径还需要进一步的详细研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bioinformatical enrichment analysis of genes involved in the pathway of endometriosis disease
Endometriosis, is a gynecological disease, where uterine (eutopic) endometrial glands and tissues are present outside the intra-uterine locations, ectopic regions (pelvic peritoneum, fallopian tubes or ovaries). About 5-10% reproductive and 20-50% infertile women have endometriosis. Several factors like hormonal, environmental, genetic and immune system are involved in the pathogenesis of endometriosis both directly or indirectly altering the estrogen level and thus affecting the reproductive health of women. Current study was done with an aim to identify novel and potential biomarker for endometriosis using mRNA seq analysis. From raw gene expression profiles differentially expressed genes (DEGs) were identified and further their functional analysis was conducted. A total of 552 (312 up and 240 downregulated) DEGs were identified in samples from endometriosis suffering women when compared with control subjects. Major DEGs forming hubnodes like C3, PSAP, APP, GNG12 were found to be involved in various functions such as, epithelia cell differentiation and development, proteolysis, gland development, muscle fiber development, response to hormone stimulus. The identified DEGs can be directly or indirectly involved in the pathway of pathogenesis of endometriosis and can act as a potential biomarker for ectopic endometrium. Current study will provide a preliminary insight into the mechanism of endometriosis disease; however, it will require further detailed studies for its complete path of action.
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