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MPFFPSDC: A multi-pooling feature fusion model for predicting synergistic drug combinations.
Bao, Xin; Sun, Jianqiang; Yi, Ming; Qiu, Jianlong; Chen, Xiangyong; Shuai, Stella C; Zhao, Qi.
Afiliação
  • Bao X; School of Automation and Electrical Engineering, Linyi University, Linyi 276000, China.
  • Sun J; School of Automation and Electrical Engineering, Linyi University, Linyi 276000, China. Electronic address: sjqyjs@sina.com.
  • Yi M; School of Mathematics and Physics, China University of Geosciences, Wuhan 430000, China.
  • Qiu J; School of Automation and Electrical Engineering, Linyi University, Linyi 276000, China.
  • Chen X; School of Automation and Electrical Engineering, Linyi University, Linyi 276000, China.
  • Shuai SC; Biological Science, Northwestern University, Evanston, IL 60208, USA.
  • Zhao Q; School of Computer Science and Software Engineering, University of Science and Technology Liaoning, Anshan 114051, China. Electronic address: zhaoqi@lnu.edu.cn.
Methods ; 217: 1-9, 2023 09.
Article em En | MEDLINE | ID: mdl-37321525
ABSTRACT
Drug combination therapies are common practice in the treatment of cancer, but not all combinations result in synergy. As traditional screening approaches are restricted in their ability to uncover synergistic drug combinations, computer-aided medicine is becoming a increasingly prevalent in this field. In this work, a predictive model of potential interactions between drugs named MPFFPSDC is presented, which can maintain the symmetry of drug inputs and eliminate inconsistencies in predictive results caused by different drug inputting sequences or positions. The experimental results show that MPFFPSDC outperforms comparative models in major performance indicators and exhibits better generalization for independent data. Furthermore, the case study demonstrates that our model can capture molecular substructures that contribute to the synergistic effect of two drugs. These results indicate that MPFFPSDC not only offers strong predictive performance, but also has good model interpretability that may provide new insights for the study of drug interaction mechanisms and the development of new drugs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Methods Assunto da revista: BIOQUIMICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Methods Assunto da revista: BIOQUIMICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China