A Deep Learning Framework for Prediction of Clinical Drug Response of Cancer Patients and Identification of Drug Sensitivity Biomarkers using Preclinical Samples
Hostallero, D. E.; Wei, L.; Wang, L.; Cairns, J.; Emad, A.
Show abstract
BackgroundPrediction of the response of cancer patients to different treatments and identification of biomarkers of drug sensitivity are two major goals of individualized medicine. In this study, we developed a deep learning framework called TINDL, completely trained on preclinical cancer cell lines, to predict the response of cancer patients to different treatments. TINDL utilizes a tissue-informed normalization to account for the tissue and cancer type of the tumours and to reduce the statistical discrepancies between cell lines and patient tumours. In addition, this model identifies a small set of genes whose mRNA expression are predictive of drug response in the trained model, enabling identification of biomarkers of drug sensitivity. ResultsUsing data from two large databases of cancer cell lines and cancer tumours, we showed that this model can distinguish between sensitive and resistant tumours for 10 (out of 14) drugs, outperforming various other machine learning models. In addition, our siRNA knockdown experiments on 10 genes identified by this model for one of the drugs (tamoxifen) confirmed that all of these genes significantly influence the drug sensitivity of the MCF7 cell line to this drug. In addition, genes implicated for multiple drugs pointed to shared mechanism of action among drugs and suggested several important signaling pathways. ConclusionsIn summary, this study provides a powerful deep learning framework for prediction of drug response and for identification of biomarkers of drug sensitivity in cancer.
Matching journals
The top 8 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Tissue-guided LASSO for prediction of clinical drug response using preclinical samples 99%
- Impact of between-tissue differences on pan-cancer predictions of drug sensitivity 97%
- A regularized functional regression model enabling transcriptome-wide dosage-dependent association study of cancer drug response 96%
Similar papers in this journal
Similar papers in this journal
- A Survey and Systematic Assessment of Computational Methods for Drug Response Prediction 95%
- GexMolGen: Cross-modal Generation of Hit-like Molecules via Large Language Model Encoding of Gene Expression Signatures 94%
- TG468: A Text Graph Convolutional Network for Predicting Clinical Response to Immune Checkpoint Inhibitor Therapy 94%
Similar papers in this journal
Similar papers in this journal
- MFmap: A semi-supervised generative model matching cell lines to tumours and cancer subtypes 96%
- Combining explainable machine learning, demographic and multi-omic data to identify precision medicine strategies for inflammatory bowel disease 95%
- Two-step multi-omics modelling of drug sensitivity in cancer cell lines to identify driving mechanisms 94%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.