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使用生物信息学分析鉴定克罗恩病和乳腺癌之间共享的关键途径和基因。

Identification of key pathways and genes shared between Crohn's disease and breast cancer using bioinformatics analysis.

作者信息

Zhou Jiang, Yang Rongcun

机构信息

State Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin 300071, P.R. China.

Key Laboratory of Bioactive Materials of The Ministry of Education, School of Medicine, Nankai University, Tianjin 300071, P.R. China.

出版信息

Oncol Lett. 2020 Oct;20(4):119. doi: 10.3892/ol.2020.11981. Epub 2020 Aug 13.

Abstract

Patients with Crohn's disease (CD) have a high risk of developing breast cancer, suggesting that there may be shared molecular mechanisms underlying CD and breast cancer. The purpose of the present study was to identify the critical genes and pathways underlying these molecular similarities using bioinformatics analysis. Publicly available microarray expression data from the Gene Expression Omnibus were analyzed, and a total of 53 overlapping differentially expressed genes (DEGs) between the CD (vs. controls) and breast cancer (vs. controls) groups were identified. These common DEGs were then subjected to Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analyses. Subsequently, a gene interaction network of the DEGs was constructed using Cytoscape software, with its plug-in cytoHubba and Molecular Complex Detection. The gene interaction network and module analysis demonstrated that prostaglandin G/H synthase 2, interleukin ()1β and were the major hub genes in the upregulated overlapping DEGs. The upregulated overlapping DEGs are found to be enriched in both the IL-17 and NF-kB signaling pathways. Taken together, the critical pathways and genes identified in the present study may help improve our understanding of why and how CD may contribute to the development of breast cancer.

摘要

克罗恩病(CD)患者患乳腺癌的风险较高,这表明CD和乳腺癌可能存在共同的分子机制。本研究的目的是通过生物信息学分析确定这些分子相似性背后的关键基因和通路。对来自基因表达综合数据库的公开可用微阵列表达数据进行了分析,共鉴定出CD组(与对照组相比)和乳腺癌组(与对照组相比)之间53个重叠的差异表达基因(DEG)。然后对这些共同的DEG进行基因本体论和京都基因与基因组百科全书通路富集分析。随后,使用Cytoscape软件及其插件cytoHubba和分子复合物检测构建了DEG的基因相互作用网络。基因相互作用网络和模块分析表明,前列腺素G/H合酶2、白细胞介素()1β和是上调的重叠DEG中的主要枢纽基因。上调的重叠DEG在IL-17和NF-κB信号通路中均富集。综上所述,本研究中确定的关键通路和基因可能有助于提高我们对CD为何以及如何促进乳腺癌发生的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c80b/7448569/925f4ade906a/ol-20-04-11981-g00.jpg

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