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首页> 外文期刊>Obesity facts : the European journal of obesity. >MicroRNA Expression Profiles in the Subcutaneous Adipose Tissues of Morbidly Obese Chinese Women
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MicroRNA Expression Profiles in the Subcutaneous Adipose Tissues of Morbidly Obese Chinese Women

机译:Microrna表达谱在病态肥胖肥胖肥胖组织中的病态肥胖肥胖组织

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摘要

Introduction: Obesity is a main global health issue and an outstanding cause of morbidity and mortality. Exploring miRNA profiling may help further studies on obesity. Methods: Three morbidly obese and 5 normal-weight Chinese women were enrolled in the microarray testing group. Abdominal subcutaneous adipose tissue (SAT) samples were excised. Total RNAs including miRNAs were extracted. Affymetrix GeneChip miRNA 4.0 Array was used to compare the expression profiles of miRNAs between the 2 groups. Two algorithms, miRanda and TargetScan, were used to predict target messenger RNAs (mRNAs). Bioinformatics analysis was then done based on the Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) databases. The sample sizes were further expanded to 8 morbidly obese and 9 normal-weight subjects, and quantitative real-time PCR (qRT-PCR) was utilized to verify the expression of differential miRNAs and target genes. Results: As per the microarray assay, 58 miRNAs were differentially expressed in the SAT from the morbidly obese and normal-weight groups (Fold 4, p 0.01, FDR 0.05); 54 of these were downregulated and 4 were upregulated in morbidly obese subjects. A total of 1,333 target genes were jointly predicted by miRanda and TargetScan. Further bioinformatics analysis showed that the differential miRNAs were involved in 269 significant biological functions and 89 significant signaling pathways. The validation experiment by qRT-PCR showed that the expression levels of miRNA-143-5p, miRNA-143-3p, miRNA-145-5p, and let-7a-5p were downregulated in morbidly obese subjects, consistent with the microarray detection. High-mobility group A2 ( HMGA2 ), a target gene of the downregulated miRNA let-7a-5p, was first found to be upregulated 3.19-fold in the SAT of morbidly obese Chinese women when compared to normal-weight controls. Conclusions: MiRNA downregulation is a hallmark of intact SAT in a morbidly obese state. Transcription (DNA-dependent), small-molecule metabolic processes, the MAPK signaling pathway, and cancer-related pathways may play important roles in the occurrence and development of obesity. For the first time, we proved that HMGA2 , a target gene of let-7a-5p, is upregulated in the SAT of morbidly obese Chinese women.
机译:介绍:肥胖是一个主要的全球健康问题,也是发病率和死亡率的杰出原因。探索miRNA分析可能有助于进一步研究肥胖症。方法:在微阵列试验组中注册了三种病态肥胖和5例正常的中国女性。切除腹部皮下脂肪组织(SAT)样品。提取包括miRNA在内的总RNA。 Affymetrix GeneChip MiRNA 4.0阵列用于比较2组之间miRNA的表达谱。两种算法,Miranda和TargetScan用于预测目标信使RNA(MRNA)。然后基于基因本体(GO)和基因组(KEGG)数据库的基因本体(GO)和京都百科全书进行生物信息学分析。样品尺寸进一步扩增至8个病态肥胖和9个正常重量受试者,并且利用定量实时PCR(QRT-PCR)来验证差异miRNA和靶基因的表达。结果:根据微阵列测定,58 miRNA在来自病态肥胖的肥胖和正常重量基团的饱和差异上表达(折叠& 4,P <0.01,FDR <0.05);其中54中可下调,4例在病态肥胖的受试者中上调。通过Miranda和TargetScan共同预测了总共1,333个靶基因。进一步的生物信息学分析表明,差异miRNA参与了269例显着的生物功能和89个显着的信号通路。 QRT-PCR的验证实验表明,MiRNA-143-5P,MiRNA-143-3P,miRNA-145-5P和Let-7A-5P的表达水平在病态肥胖的受试者中下调,与微阵列检测一致。首先发现高迁移率组A2(HMGA2),下调MiRNA Let-7A-5P的靶基因,在与正常重量控制相比,在病态肥胖肥胖的肥胖肥胖的六个六个左右上升3.19倍。结论:MiRNA下调是一个在病态肥胖状态下完整的标志。转录(DNA依赖性),小分子代谢过程,MAPK信号通路和癌症相关途径可能在肥胖的发生和发展中起重要作用。我们首次证明HMGA2是Let-7A-5P的靶基因,在病态肥胖的肥胖肥胖肥胖的六个患者中上调。

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