Context-specific functional module based drug efficacy prediction

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Background: It is necessary to evaluate the efficacy of individual drugs on patients to realize personalized medicine. Testing drugs on patients in clinical trial is the only way to evaluate the efficacy of drugs. The approach is labour intensive and requires overwhelming costs and a number of experiments. Therefore, preclinical model system has been intensively investigated for predicting the efficacy of drugs. Current computational drug sensitivity prediction approaches use general biological network modules as their prediction features. Therefore, they miss indirect effectors or the effects from tissue-specific interactions. Results: We developed cell line specific functional modules. Enriched scores of functional modules are utilized as cell line specific features to predict the efficacy of drugs. Cell line specific functional modules are clusters of genes, which have similar biological functions in cell line specific networks. We used linear regression for drug efficacy prediction. We assessed the prediction performance in leave-one-out cross-validation (LOOCV). Our method was compared with elastic net model, which is a popular model for drug efficacy prediction. In addition, we analysed drug sensitivity-associated functions of five drugs - lapatinib, erlotinib, raloxifene, tamoxifen and gefitinib-by our model. Conclusions: Our model can provide cell line specific drug efficacy prediction and also provide functions which are associated with drug sensitivity. Therefore, we could utilize drug sensitivity associated functions for drug repositioning or for suggesting secondary drugs for overcoming drug resistance.
Publisher
BIOMED CENTRAL LTD
Issue Date
2016-07
Language
English
Article Type
Article; Proceedings Paper
Keywords

BREAST-CANCER; LUNG-CANCER; SENSITIVITY; RESISTANCE; CELLS; ENCYCLOPEDIA; GEFITINIB; NETWORKS; TARGETS

Citation

BMC BIOINFORMATICS, v.17, no.S6, pp.275

ISSN
1471-2105
DOI
10.1186/s12859-016-1078-6
URI
http://hdl.handle.net/10203/219679
Appears in Collection
BiS-Journal Papers(저널논문)
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