Perfil diferencial de transcritos em endométrio eutópico de mulheres inférteis com endometriose e controles durante a janela de implantação

Michele Gomes Da Broi , Carlos Valério Rocha‐Junior , Jessica Rodrigues Plaça , Wilson Araujo Silva Jr. , Rui Alberto Ferriani , Paula Andrea Navarro
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Abstract

Objectives

Molecular alterations in the eutopic endometrium of women with endometriosis may be involved in the endometriosis‐related infertility. This study aimed to compare the differentially expressed genes (DEG) in eutopic endometrium of infertile women with endometriosis, infertile controls (IC; male and/or tubal factor) and fertile controls (FC) through RNA‐Seq.

Material and methods

Endometrial biopsies were obtained from 17 patiens (6 infertile women with endometriosis, 6 IC and 5 FC) during the implantation window. The RNA was extracted and the RNA‐Seq was performed at a HISEQ 2500 Illumina Platform, high output, paired end. Standardization and differential expression were conducted in the statistical R environment using DESeq2 package.

Results

The groups IC and FC were similar. No DEG has been identified comparing CF and endometriosis groups. Five DEGs (SCUBE1, CCL20, LGALS9 C, TRIM 29 e WNT11) were identified in the advanced endometriosis (EIII/IV) group, and 1 (KANSL1‐AS1) in the initial endometriosis (EI/II) group compared to FC. Two DEGs (KANSL1‐AS1 and VGLL3) were identified by comparing EI/II and EIII/IV groups.

Conclusions

These data suggest that the eutopic endometrium of infertile women with endometriosis, especially those with advanced disease, may be molecularly different from those of fertile women during the implantation window.

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子宫内膜异位症不孕妇女和对照组在着床窗口期正常子宫内膜转录本的差异图谱
目的探讨子宫内膜异位症患者异位子宫内膜的分子改变可能与子宫内膜异位症相关的不孕症有关。本研究旨在比较子宫内膜异位症不孕妇女异位子宫内膜差异表达基因(DEG)、不孕对照(IC;男性和/或输卵管因子)和生育对照(FC)通过RNA‐Seq。材料与方法对17例患者(6例伴有子宫内膜异位症的不孕妇女,6例子宫内膜异位症,5例子宫内膜异位症)在着床窗期进行子宫活检。提取RNA,并在HISEQ 2500 Illumina平台上进行RNA‐Seq,高输出,配对端。使用DESeq2软件包在统计R环境下进行标准化和差异表达。结果IC组与FC组相似。未发现CF组和子宫内膜异位症组的DEG比较。与FC相比,在晚期子宫内膜异位症(EIII/IV)组中鉴定出5个基因(SCUBE1、CCL20、lgals9c、TRIM 29和WNT11),在初始子宫内膜异位症(EI/II)组中鉴定出1个基因(KANSL1‐AS1)。通过比较EI/II组和EIII/IV组,鉴定出两个DEGs (KANSL1‐AS1和VGLL3)。结论伴有子宫内膜异位症的不孕症患者,特别是晚期疾病患者的异位子宫内膜在着床窗期可能与正常受孕女性的异位子宫内膜存在分子差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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