Zhang Yi, Chen Min, Cheng Xiaohui, Wei Hanyan
School of Information Science and Engineering, Guilin University of Technology, Guilin, China.
School of Computer Science and Technology, Hunan Institute of Technology, Hengyang, China.
Front Genet. 2020 Apr 30;11:389. doi: 10.3389/fgene.2020.00389. eCollection 2020.
Growing evidences have indicated that microRNAs (miRNAs) play a significant role relating to many important bioprocesses; their mutations and disorders will cause the occurrence of various complex diseases. The prediction of miRNAs associated with underlying diseases computational approaches is beneficial to identify biomarkers and discover specific medicine, which can greatly reduce the cost of diagnosis, cure, prognosis, and prevention of human diseases. However, how to further achieve a more reliable prediction of potential miRNA-disease associations with effective integration of different biological data is a challenge for researchers. In this study, we proposed a computational model by using a federated method of combined multiple-similarities fusion and space projection (MSFSP). MSFSP firstly fused the integrated disease similarity (composed of disease semantic similarity, disease functional similarity, and disease Hamming similarity) with the integrated miRNA similarity (composed of miRNA functional similarity, miRNA sequence similarity, and miRNA Hamming similarity). Secondly, it constructed the weighted network of miRNA-disease associations from the experimentally verified Boolean network of miRNA-disease associations by using similarity networks. Finally, it calculated the prediction results by weighting miRNA space projection scores and the disease space projection scores. Leave-one-out cross-validation demonstrated that MSFSP has the distinguished predictive accuracy with area under the receiver operating characteristics curve (AUC) of 0.9613 better than that of five other existing models. In case studies, the predictive ability of MSFSP was further confirmed as 96 and 98% of the top 50 predictions for prostatic neoplasms and lung neoplasms were successfully validated by experimental evidences and supporting experimental evidences were also found for 100% of the top 50 predictions for isolated diseases.
越来越多的证据表明,微小RNA(miRNA)在许多重要的生物过程中发挥着重要作用;它们的突变和紊乱会导致各种复杂疾病的发生。通过计算方法预测与潜在疾病相关的miRNA,有利于识别生物标志物和发现特效药物,这可以大大降低人类疾病诊断、治疗、预后和预防的成本。然而,如何通过有效整合不同的生物数据进一步实现对潜在miRNA-疾病关联的更可靠预测,对研究人员来说是一个挑战。在本研究中,我们提出了一种计算模型,即使用多相似性融合与空间投影相结合的联邦方法(MSFSP)。MSFSP首先将整合的疾病相似性(由疾病语义相似性、疾病功能相似性和疾病汉明相似性组成)与整合的miRNA相似性(由miRNA功能相似性、miRNA序列相似性和miRNA汉明相似性组成)进行融合。其次,通过相似性网络,从经实验验证的miRNA-疾病关联布尔网络构建miRNA-疾病关联加权网络。最后,通过对miRNA空间投影得分和疾病空间投影得分进行加权计算预测结果。留一法交叉验证表明,MSFSP具有卓越的预测准确性,其受试者工作特征曲线下面积(AUC)为0.9613,优于其他五个现有模型。在案例研究中,MSFSP的预测能力进一步得到证实,前列腺肿瘤和肺肿瘤前50个预测中有96%和98%被实验证据成功验证,对于孤立疾病的前50个预测中,100%也找到了支持性实验证据。