School of Computer Science and Software Engineering, University of Science and Technology Liaoning, Anshan, China.
School of Electronic and Information Engineering, University of Science and Technology Liaoning, Anshan, China.
J Cell Mol Med. 2024 Oct;28(19):e18591. doi: 10.1111/jcmm.18591.
The unique non-coding RNA molecule known as circular RNA (circRNA) is distinguished from conventional linear RNA by having a longer half-life, greater degree of conservation and inherent solidity. Extensive research has demonstrated the profound impact of circRNA expression on cellular drug sensitivity and therapeutic efficacy. There is an immediate need for the creation of efficient computational techniques to anticipate the potential correlations between circRNA and drug sensitivity, as classical biological research approaches are time-consuming and costly. In this work, we introduce a novel deep learning model called SNMGCDA, which aims to forecast the relationships between circRNA and drug sensitivity. SNMGCDA incorporates a diverse range of similarity networks, enabling the derivation of feature vectors for circRNAs and drugs using three distinct calculation methods. First, we utilize a sparse autoencoder for the extraction of drug characteristics. Subsequently, the application of non-negative matrix factorization (NMF) enables the identification of relationships between circRNAs and drugs based on their shared features. Additionally, the multi-head graph attention network is employed to capture the characteristics of circRNAs. After acquiring the characteristics from these three separate components, we combine them to form a unified and inclusive feature vector for each cluster of circRNA and drug. Finally, the relevant feature vectors and labels are inputted into a multilayer perceptron (MLP) to make predictions. The outcomes of the experiment, obtained through 5-fold cross-validation (5-fold CV) and 10-fold cross-validation (10-fold CV), demonstrate SNMGCDA outperforms five other state-of-art methods in terms of performance. Additionally, the majority of case studies have predominantly confirmed newly discovered correlations by SNMGCDA, thereby emphasizing its reliability in predicting potential relationships between circRNAs and drugs.
一种被称为环状 RNA(circRNA)的独特非编码 RNA 分子,与常规线性 RNA 不同,其半衰期更长、保守性更高且具有固有的稳定性。大量研究表明,circRNA 的表达对细胞药物敏感性和治疗效果有深远的影响。目前迫切需要创建有效的计算技术,以预测 circRNA 与药物敏感性之间的潜在相关性,因为经典的生物学研究方法既耗时又昂贵。在这项工作中,我们引入了一种名为 SNMGCDA 的新型深度学习模型,旨在预测 circRNA 与药物敏感性之间的关系。SNMGCDA 结合了多种相似性网络,使用三种不同的计算方法为 circRNA 和药物推导特征向量。首先,我们使用稀疏自编码器提取药物特征。然后,应用非负矩阵分解(NMF)可以根据 circRNA 和药物的共享特征识别它们之间的关系。此外,采用多头图注意网络捕获 circRNA 的特征。从这三个独立的组件中获取特征后,我们将它们组合在一起,为每个 circRNA 和药物簇形成一个统一的综合特征向量。最后,将相关特征向量和标签输入多层感知机(MLP)进行预测。通过 5 倍交叉验证(5-fold CV)和 10 倍交叉验证(10-fold CV)获得的实验结果表明,SNMGCDA 在性能方面优于其他五种最先进的方法。此外,大多数案例研究主要证实了 SNMGCDA 新发现的相关性,从而强调了其在预测 circRNA 和药物之间潜在关系方面的可靠性。