Systematically identify key genes in inflammatory and non-inflammatory breast cancer

被引:25
作者
Chai, Fan [1 ]
Liang, Yan [1 ]
Zhang, Fan [1 ]
Wang, Minghao [1 ]
Zhong, Ling [1 ]
Jiang, Jun [1 ]
机构
[1] Third Mil Med Univ, Southwest Hosp, Breast Dis Ctr, Chongqing 400038, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Tumor microenvironment; Inflammatory breast cancer; non-inflammatory breast cancer; PDGFR beta; SUMO1 and COL1A1; RECEPTOR-BETA; CELL-MIGRATION; METASTASIS; OVEREXPRESSION; ANGIOGENESIS; SUMOYLATION; EXPRESSION; CARCINOMA; PATHWAYS; PROTEIN;
D O I
10.1016/j.gene.2015.09.025
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Although the gene expression in breast tumor stroma, playing a critical role in determining inflammatory breast cancer (IBC) phenotype, has been proved to be significantly different between IBC and non-inflammatory breast cancer (non-IBC), more effort needs to systematically investigate the gene expression profiles between tumor epithelium and stroma and to efficiently uncover the potential molecular networks and critical genes for IBC and non-IBC. Here, we comprehensively analyzed and compared the transcriptional profiles from IBC and non-IBC patients using hierarchical clustering, protein-protein interaction (PPI) network, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) database analyses, and identified PDGFR beta, SUMO1, COL1A1, FYN, CAV1, COL5A1 and MMP2 to be the key genes for breast cancer. Interestingly, PDGFR beta was found to be the hub gene in both IBC and non-IBC; SUMO1 and COL1A1 were respectively the key genes for IBC and non-IBC. These analysis results indicated that those key genes might play important role in IBC and non-IBC and provided some clues for future studies. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:600 / 614
页数:15
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