TY - JOUR
T1 - MCMVDRP
T2 - a multi-channel multi-view deep learning framework for cancer drug response prediction
AU - Li, Xiangyu
AU - Shi, Xiumin
AU - Li, Yuxuan
AU - Wang, Lu
N1 - Publisher Copyright:
© 2024 the author(s), published by De Gruyter, Berlin/Boston.
PY - 2024/9/1
Y1 - 2024/9/1
N2 - Drug therapy remains the primary approach to treating tumours. Variability among cancer patients, including variations in genomic profiles, often results in divergent therapeutic responses to analogous anti-cancer drug treatments within the same cohort of cancer patients. Hence, predicting the drug response by analysing the genomic profile characteristics of individual patients holds significant research importance. With the notable progress in machine learning and deep learning, many effective methods have emerged for predicting drug responses utilizing features from both drugs and cell lines. However, these methods are inadequate in capturing a sufficient number of features inherent to drugs. Consequently, we propose a representational approach for drugs that incorporates three distinct types of features: the molecular graph, the SMILE strings, and the molecular fingerprints. In this study, a novel deep learning model, named MCMVDRP, is introduced for the prediction of cancer drug responses. In our proposed model, an amalgamation of these extracted features is performed, followed by the utilization of fully connected layers to predict the drug response based on the IC50 values. Experimental results demonstrate that the presented model outperforms current state-of-the-art models in performance.
AB - Drug therapy remains the primary approach to treating tumours. Variability among cancer patients, including variations in genomic profiles, often results in divergent therapeutic responses to analogous anti-cancer drug treatments within the same cohort of cancer patients. Hence, predicting the drug response by analysing the genomic profile characteristics of individual patients holds significant research importance. With the notable progress in machine learning and deep learning, many effective methods have emerged for predicting drug responses utilizing features from both drugs and cell lines. However, these methods are inadequate in capturing a sufficient number of features inherent to drugs. Consequently, we propose a representational approach for drugs that incorporates three distinct types of features: the molecular graph, the SMILE strings, and the molecular fingerprints. In this study, a novel deep learning model, named MCMVDRP, is introduced for the prediction of cancer drug responses. In our proposed model, an amalgamation of these extracted features is performed, followed by the utilization of fully connected layers to predict the drug response based on the IC50 values. Experimental results demonstrate that the presented model outperforms current state-of-the-art models in performance.
KW - bidirectional long short-term memory
KW - convolutional neural network
KW - deep learning
KW - drug response prediction
KW - graph convolutional network
UR - http://www.scopus.com/inward/record.url?scp=85211393647&partnerID=8YFLogxK
U2 - 10.1515/jib-2024-0026
DO - 10.1515/jib-2024-0026
M3 - Article
C2 - 39238451
AN - SCOPUS:85211393647
SN - 1613-4516
VL - 21
JO - Journal of integrative bioinformatics
JF - Journal of integrative bioinformatics
IS - 3
ER -