Chen Yi-Xiao, Rong Yu, Jiang Feng, Chen Jia-Bin, Duan Yuan-Yuan, Dong Shan-Shan, Zhu Dong-Li, Chen Hao, Yang Tie-Lin, Dai Zhijun, Guo Yan
Key Laboratory of Biomedical Information Engineering of Ministry of Education, Biomedical Informatics & Genomics Center, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an, Shaanxi Province 710049, PR China.
Research Institute of Xi'an Jiaotong University, Zhejiang Province 311215, PR China.
Comput Struct Biotechnol J. 2020 Oct 8;18:2826-2835. doi: 10.1016/j.csbj.2020.10.001. eCollection 2020.
Although genome-wide association studies (GWASs) have successfully identified thousands of risk variants for human complex diseases, understanding the biological function and molecular mechanisms of the associated SNPs involved in complex diseases is challenging. Here we developed a framework named integrative multi-omics network-based approach (IMNA), aiming to identify potential key genes in regulatory networks by integrating molecular interactions across multiple biological scales, including GWAS signals, gene expression-based signatures, chromatin interactions and protein interactions from the network topology. We applied this approach to breast cancer, and prioritized key genes involved in regulatory networks. We also developed an abnormal gene expression score (AGES) signature based on the gene expression deviation of the top 20 rank-ordered genes in breast cancer. The AGES values are associated with genetic variants, tumor properties and patient survival outcomes. Among the top 20 genes, was identified as a new candidate gene for breast cancer. Thus, our integrative network-based approach provides a genetic-driven framework to unveil tissue-specific interactions from multiple biological scales and reveal potential key regulatory genes for breast cancer. This approach can also be applied in other complex diseases such as ovarian cancer to unravel underlying mechanisms and help for developing therapeutic targets.
尽管全基因组关联研究(GWAS)已成功识别出数千种人类复杂疾病的风险变异,但了解复杂疾病相关单核苷酸多态性(SNP)的生物学功能和分子机制仍具有挑战性。在此,我们开发了一种名为基于整合多组学网络的方法(IMNA)的框架,旨在通过整合跨多个生物尺度的分子相互作用来识别调控网络中的潜在关键基因,这些相互作用包括GWAS信号、基于基因表达的特征、染色质相互作用以及来自网络拓扑结构的蛋白质相互作用。我们将此方法应用于乳腺癌,并对调控网络中涉及的关键基因进行了优先级排序。我们还基于乳腺癌中排名前20的基因的基因表达偏差开发了一种异常基因表达评分(AGES)特征。AGES值与遗传变异、肿瘤特性和患者生存结果相关。在前20个基因中, 被确定为乳腺癌的一个新候选基因。因此,我们基于整合网络的方法提供了一个遗传驱动的框架,以揭示来自多个生物尺度的组织特异性相互作用,并揭示乳腺癌潜在的关键调控基因。这种方法也可应用于其他复杂疾病,如卵巢癌,以阐明潜在机制并有助于开发治疗靶点。