GAM-MDR: probing miRNA–drug resistance using a graph autoencoder based on random path masking

Author:

Zhou Zhecheng1,Du Zhenya2,Jiang Xin1,Zhuo Linlin1,Xu Yixin3,Fu Xiangzheng4,Liu Mingzhe1,Zou Quan5

Affiliation:

1. Wenzhou University of Technology , 325000, Wenzhou , China

2. Guangzhou Xinhua University , 510520, Guangzhou , China

3. West China School of Pharmacy Sichuan University , 610041, Chengdu , China

4. College of Computer Science and Electronic Engineering, Hunan University , 410006, Changsha , China

5. Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China , 611730, Chengdu , China

Abstract

Abstract MicroRNAs (miRNAs) are found ubiquitously in biological cells and play a pivotal role in regulating the expression of numerous target genes. Therapies centered around miRNAs are emerging as a promising strategy for disease treatment, aiming to intervene in disease progression by modulating abnormal miRNA expressions. The accurate prediction of miRNA–drug resistance (MDR) is crucial for the success of miRNA therapies. Computational models based on deep learning have demonstrated exceptional performance in predicting potential MDRs. However, their effectiveness can be compromised by errors in the data acquisition process, leading to inaccurate node representations. To address this challenge, we introduce the GAM-MDR model, which combines the graph autoencoder (GAE) with random path masking techniques to precisely predict potential MDRs. The reliability and effectiveness of the GAM-MDR model are mainly reflected in two aspects. Firstly, it efficiently extracts the representations of miRNA and drug nodes in the miRNA–drug network. Secondly, our designed random path masking strategy efficiently reconstructs critical paths in the network, thereby reducing the adverse impact of noisy data. To our knowledge, this is the first time that a random path masking strategy has been integrated into a GAE to infer MDRs. Our method was subjected to multiple validations on public datasets and yielded promising results. We are optimistic that our model could offer valuable insights for miRNA therapeutic strategies and deepen the understanding of the regulatory mechanisms of miRNAs. Our data and code are publicly available at GitHub:https://github.com/ZZCrazy00/GAM-MDR.

Publisher

Oxford University Press (OUP)

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