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鉴定和验证与多囊卵巢综合征和代谢综合征相关的核心基因。

Identification and validation of core genes associated with polycystic ovary syndrome and metabolic syndrome.

机构信息

Reproductive Medicine Center, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.

Reproductive Medicine Center, The Southwest Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.

出版信息

Medicine (Baltimore). 2024 Oct 18;103(42):e40162. doi: 10.1097/MD.0000000000040162.

Abstract

Polycystic ovary syndrome (PCOS) is a common endocrine and metabolic disorder affecting women of reproductive age, affecting reproductive health, and increasing the incidence of diabetes mellitus and hypertension. Metabolic syndrome (MetS) is the most common metabolic disorder. Although clinical studies have shown a close association between PCOS and MetS, the molecular mechanisms are unknown. In this study, datasets of PCOS and MetS were obtained from the Gene Expression Omnibus database; differential expression analysis and weighted gene coexpression network analysis (WGCNA) were performed; and gene ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses also performed of differentially expressed genes (DEGs). The PCOS- and MetS-coexpressed DEGs were subsequently intersected with the coexpressed genes in the WGCNA module to obtain the core genes. By constructing receiver operating characteristic curves, we verified the predictive effects of the core genes. We also validated the expression of the core genes in the datasets. Finally, we verified the expression of the core genes by quantitative polymerase chain reaction in human follicular fluid granulosa cells. In addition, we used Cell-type Identification By Estimating Relative Subsets Of RNA Transcripts to analyze the immune infiltration of immune cells in PCOS and MetS. Finally, we obtained 52 coexpressed DEGs of PCOS and MetS and 3 coexpressed genes in the WGCNA module. By taking the intersection of coexpressed DEGs and coexpressed genes of the WGCNA module, we get ELOVL fatty acid elongase 7 (ELOVL7) as the core gene. Receiver operating characteristic curve analysis showed that ELOVL7 is a reliable biological marker for PCOS and MetS. The expression level of ELOVL7 in human follicular fluid granulosa cells from PCOS patients was significantly higher than that of controls, as verified by quantitative polymerase chain reaction. This study provides the first evidence of the role of ELOVL7 in developing PCOS and MetS. This gene may serve as a potential diagnostic marker and therapeutic target for both conditions.

摘要

多囊卵巢综合征(PCOS)是一种常见的影响育龄期妇女的内分泌和代谢紊乱疾病,它会影响生殖健康,并增加糖尿病和高血压的发病率。代谢综合征(MetS)是最常见的代谢紊乱。虽然临床研究表明 PCOS 与 MetS 之间存在密切关联,但分子机制尚不清楚。在这项研究中,从基因表达综合数据库中获取了 PCOS 和 MetS 的数据集;进行了差异表达分析和加权基因共表达网络分析(WGCNA);并对差异表达基因(DEGs)进行了基因本体和京都基因与基因组百科全书富集分析。随后,将 PCOS 和 MetS 共表达的 DEGs 与 WGCNA 模块中的共表达基因进行交集,获得核心基因。通过构建受试者工作特征曲线,验证了核心基因的预测效果。我们还验证了数据集核心基因的表达。最后,我们通过人类卵泡液颗粒细胞中的定量聚合酶链反应验证了核心基因的表达。此外,我们使用通过估计相对 RNA 转录物子集来鉴定细胞类型,分析了 PCOS 和 MetS 中免疫细胞的免疫浸润。最后,我们得到了 52 个 PCOS 和 MetS 的共表达 DEG 和 WGCNA 模块中的 3 个共表达基因。通过取共表达 DEG 和 WGCNA 模块的共表达基因的交集,得到 ELOVL 脂肪酸延长酶 7(ELOVL7)作为核心基因。受试者工作特征曲线分析表明,ELOVL7 是 PCOS 和 MetS 的可靠生物标志物。通过定量聚合酶链反应验证,从 PCOS 患者的人类卵泡液颗粒细胞中获得的 ELOVL7 表达水平明显高于对照组。这项研究首次提供了 ELOVL7 在 PCOS 和 MetS 发病机制中的作用证据。该基因可能作为这两种疾病的潜在诊断标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8801/11495751/32c29dcdeb15/medi-103-e40162-g001.jpg

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