Li Jie, Wu Zengrui, Cheng Feixiong, Li Weihua, Liu Guixia, Tang Yun
Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China.
1] Shanghai Key Laboratory of New Drug Design, School of Pharmacy, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China [2] Key Laboratory of Cigarette Smoke, Technical Center, Shanghai Tobacco Group Co. Ltd., Shanghai 200082, China.
Sci Rep. 2014 Jul 4;4:5576. doi: 10.1038/srep05576.
MicroRNAs (miRNAs) play important roles in multiple biological processes and have attracted much scientific attention recently. Their expression can be altered by environmental factors (EFs), which are associated with many diseases. Identification of the phenotype-genotype relationships among miRNAs, EFs, and diseases at the network level will help us to better understand toxicology mechanisms and disease etiologies. In this study, we developed a computational systems toxicology framework to predict new associations among EFs, miRNAs and diseases by integrating EF structure similarity and disease phenotypic similarity. Specifically, three comprehensive bipartite networks: EF-miRNA, EF-disease and miRNA-disease associations, were constructed to build predictive models. The areas under the receiver operating characteristic curves using 10-fold cross validation ranged from 0.686 to 0.910. Furthermore, we successfully inferred novel EF-miRNA-disease networks in two case studies for breast cancer and cigarette smoke. Collectively, our methods provide a reliable and useful tool for the study of chemical risk assessment and disease etiology involving miRNAs.
微小RNA(miRNAs)在多个生物学过程中发挥重要作用,近年来已引起科学界的广泛关注。它们的表达可被环境因素(EFs)改变,而环境因素与许多疾病相关。在网络层面识别微小RNA、环境因素和疾病之间的表型-基因型关系,将有助于我们更好地理解毒理学机制和疾病病因。在本研究中,我们开发了一种计算系统毒理学框架,通过整合环境因素结构相似性和疾病表型相似性来预测环境因素、微小RNA和疾病之间的新关联。具体而言,构建了三个综合二分网络:环境因素-微小RNA、环境因素-疾病和微小RNA-疾病关联,以建立预测模型。使用10折交叉验证的受试者工作特征曲线下面积范围为0.686至0.910。此外,我们在乳腺癌和香烟烟雾的两个案例研究中成功推断出了新的环境因素-微小RNA-疾病网络。总体而言,我们的方法为涉及微小RNA的化学风险评估和疾病病因研究提供了一个可靠且有用的工具。