Deep contrastive learning for predicting cancer prognosis using gene expression values.

Autor: Sun A; Department of Electrical and Computer Engineering, University of Miami, Miami, FL 33146, United States., Franzmann EJ; Department of Otolaryngology, University of Miami, Miami, FL 33146, United States.; Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL 33146, United States., Chen Z; Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL 33146, United States.; Department of Microbiology and Immunology, University of Miami, Miami, FL 33146, United States., Cai X; Department of Electrical and Computer Engineering, University of Miami, Miami, FL 33146, United States.; Sylvester Comprehensive Cancer Center, University of Miami, Miami, FL 33146, United States.
Jazyk: angličtina
Zdroj: Briefings in bioinformatics [Brief Bioinform] 2024 Sep 23; Vol. 25 (6).
DOI: 10.1093/bib/bbae544
Abstrakt: Recent advancements in image classification have demonstrated that contrastive learning (CL) can aid in further learning tasks by acquiring good feature representation from a limited number of data samples. In this paper, we applied CL to tumor transcriptomes and clinical data to learn feature representations in a low-dimensional space. We then utilized these learned features to train a classifier to categorize tumors into a high- or low-risk group of recurrence. Using data from The Cancer Genome Atlas (TCGA), we demonstrated that CL can significantly improve classification accuracy. Specifically, our CL-based classifiers achieved an area under the receiver operating characteristic curve (AUC) greater than 0.8 for 14 types of cancer, and an AUC greater than 0.9 for 3 types of cancer. We also developed CL-based Cox (CLCox) models for predicting cancer prognosis. Our CLCox models trained with the TCGA data outperformed existing methods significantly in predicting the prognosis of 19 types of cancer under consideration. The performance of CLCox models and CL-based classifiers trained with TCGA lung and prostate cancer data were validated using the data from two independent cohorts. We also show that the CLCox model trained with the whole transcriptome significantly outperforms the Cox model trained with the 16 genes of Oncotype DX that is in clinical use for breast cancer patients. The trained models and the Python codes are publicly accessible and provide a valuable resource that will potentially find clinical applications for many types of cancer.
(© The Author(s) 2024. Published by Oxford University Press.)
Databáze: MEDLINE
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