Your browser doesn't support javascript.
loading
MFSynDCP: multi-source feature collaborative interactive learning for drug combination synergy prediction.
Dong, Yunyun; Chang, Yunqing; Wang, Yuxiang; Han, Qixuan; Wen, Xiaoyuan; Yang, Ziting; Zhang, Yan; Qiang, Yan; Wu, Kun; Fan, Xiaole; Ren, Xiaoqiang.
Afiliação
  • Dong Y; School of Software, Taiyuan University of Technology, Taiyuan, Shanxi, China. dongyunyun@tyut.edu.cn.
  • Chang Y; School of Software, Taiyuan University of Technology, Taiyuan, Shanxi, China.
  • Wang Y; School of Software, Taiyuan University of Technology, Taiyuan, Shanxi, China.
  • Han Q; School of Software, Taiyuan University of Technology, Taiyuan, Shanxi, China.
  • Wen X; School of Software, Taiyuan University of Technology, Taiyuan, Shanxi, China.
  • Yang Z; School of Software, Taiyuan University of Technology, Taiyuan, Shanxi, China.
  • Zhang Y; School of Software, Taiyuan University of Technology, Taiyuan, Shanxi, China.
  • Qiang Y; College of Computer Science and Technology (College of Data Science), Taiyuan University of Technology, Taiyuan, Shanxi, China. qiangyan@tyut.edu.cn.
  • Wu K; School of Computing, University of Leeds, Leeds, West Yorkshire, UK.
  • Fan X; Information Management Department, Shanxi Provincial People's Hospital, Taiyuan, Shanxi, China.
  • Ren X; Information Management Department, Shanxi Provincial People's Hospital, Taiyuan, Shanxi, China.
BMC Bioinformatics ; 25(1): 140, 2024 Apr 01.
Article em En | MEDLINE | ID: mdl-38561679
ABSTRACT
Drug combination therapy is generally more effective than monotherapy in the field of cancer treatment. However, screening for effective synergistic combinations from a wide range of drug combinations is particularly important given the increase in the number of available drug classes and potential drug-drug interactions. Existing methods for predicting the synergistic effects of drug combinations primarily focus on extracting structural features of drug molecules and cell lines, but neglect the interaction mechanisms between cell lines and drug combinations. Consequently, there is a deficiency in comprehensive understanding of the synergistic effects of drug combinations. To address this issue, we propose a drug combination synergy prediction model based on multi-source feature interaction learning, named MFSynDCP, aiming to predict the synergistic effects of anti-tumor drug combinations. This model includes a graph aggregation module with an adaptive attention mechanism for learning drug interactions and a multi-source feature interaction learning controller for managing information transfer between different data sources, accommodating both drug and cell line features. Comparative studies with benchmark datasets demonstrate MFSynDCP's superiority over existing methods. Additionally, its adaptive attention mechanism graph aggregation module identifies drug chemical substructures crucial to the synergy mechanism. Overall, MFSynDCP is a robust tool for predicting synergistic drug combinations. The source code is available from GitHub at https//github.com/kkioplkg/MFSynDCP .
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Benchmarking / Treinamento por Simulação Idioma: En Revista: BMC Bioinformatics Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Benchmarking / Treinamento por Simulação Idioma: En Revista: BMC Bioinformatics Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China