Machine learning on syngeneic mouse tumor profiles to model clinical immunotherapy response.
Zexian ZengShengqing Stan GuCheryl J WongLin YangNofal OuardaouiDian LiWubing ZhangMyles A BrownX Shirley LiuPublished in: Science advances (2022)
Most patients with cancer are refractory to immune checkpoint blockade (ICB) therapy, and proper patient stratification remains an open question. Primary patient data suffer from high heterogeneity, low accessibility, and lack of proper controls. In contrast, syngeneic mouse tumor models enable controlled experiments with ICB treatments. Using transcriptomic and experimental variables from >700 ICB-treated/control syngeneic mouse tumors, we developed a machine learning framework to model tumor immunity and identify factors influencing ICB response. Projected on human immunotherapy trial data, we found that the model can predict clinical ICB response. We further applied the model to predicting ICB-responsive/resistant cancer types in The Cancer Genome Atlas, which agreed well with existing clinical reports. Last, feature analysis implicated factors associated with ICB response. In summary, our computational framework based on mouse tumor data reliably stratified patients regarding ICB response, informed resistance mechanisms, and has the potential for wide applications in disease treatment studies.
Keyphrases
- machine learning
- big data
- electronic health record
- single cell
- papillary thyroid
- squamous cell carcinoma
- ejection fraction
- endothelial cells
- emergency department
- climate change
- gene expression
- mesenchymal stem cells
- risk assessment
- randomized controlled trial
- case report
- data analysis
- young adults
- dna methylation
- rna seq
- genome wide
- human health
- induced pluripotent stem cells
- pluripotent stem cells