School of Computer Science and Engineering, South China University of Technology, Guangzhou 510006, China.
School of Computer, Electronics and Information, Guangxi University, Nanning 530004, China.
Biomed Res Int. 2021 Feb 23;2021:6652948. doi: 10.1155/2021/6652948. eCollection 2021.
The existing studies have shown that miRNAs are related to human diseases by regulating gene expression. Identifying miRNA association with diseases will contribute to diagnosis, treatment, and prognosis of diseases. The experimental identification of miRNA-disease associations is time-consuming, tremendously expensive, and of high-failure rate. In recent years, many researchers predicted potential associations between miRNAs and diseases by computational approaches. In this paper, we proposed a novel method using deep collaborative filtering called DCFMDA to predict miRNA-disease potential associations. To improve prediction performance, we integrated neural network matrix factorization (NNMF) and multilayer perceptron (MLP) in a deep collaborative filtering framework. We utilized known miRNA-disease associations to capture miRNA-disease interaction features by NNMF and utilized miRNA similarity and disease similarity to extract miRNA feature vector and disease feature vector, respectively, by MLP. At last, we merged outputs of the NNMF and MLP to obtain the prediction matrix. The experimental results indicate that compared with other existing computational methods, our method can achieve the AUC of 0.9466 based on 10-fold cross-validation. In addition, case studies show that the DCFMDA can effectively predict candidate miRNAs for breast neoplasms, colon neoplasms, kidney neoplasms, leukemia, and lymphoma.
现有研究表明,miRNA 通过调控基因表达与人类疾病有关。鉴定 miRNA 与疾病的关联有助于疾病的诊断、治疗和预后。miRNA 与疾病关联的实验鉴定既耗时、费用高昂,又失败率高。近年来,许多研究人员通过计算方法预测 miRNA 与疾病之间的潜在关联。在本文中,我们提出了一种使用深度协同过滤的新方法,称为 DCFMDA,用于预测 miRNA-疾病的潜在关联。为了提高预测性能,我们在深度协同过滤框架中集成了神经网络矩阵分解(NNMF)和多层感知机(MLP)。我们利用已知的 miRNA-疾病关联,通过 NNMF 捕获 miRNA-疾病相互作用特征,利用 miRNA 相似性和疾病相似性,通过 MLP 分别提取 miRNA 特征向量和疾病特征向量。最后,我们合并 NNMF 和 MLP 的输出,得到预测矩阵。实验结果表明,与其他现有计算方法相比,我们的方法在 10 折交叉验证中可以达到 0.9466 的 AUC。此外,案例研究表明,DCFMDA 可以有效地预测乳腺癌、结肠癌、肾癌、白血病和淋巴瘤的候选 miRNA。