4.6 Article

Moanna: Multi-Omics Autoencoder-Based Neural Network Algorithm for Predicting Breast Cancer Subtypes

Journal

IEEE ACCESS
Volume 11, Issue -, Pages 10912-10924

Publisher

IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/ACCESS.2023.3240515

Keywords

Breast cancer; Gene expression; Cancer; Deep learning; Neural networks; Tumors; Feature extraction; Artificial neural networks; Genomics; Bioinformatics; cancer subtyping; artificial neural networks; machine learning; classification algorithms; cancer genomics; bioinformatics; genetic expression; deep learning; artificial intelligence

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Cancer subtyping provides valuable insights and is an essential step toward personalized medicine. However, recent studies have highlighted inconsistencies in breast cancer subtype classifications, indicating the need for optimization. We propose a deep-learning-based algorithm, Moanna, that integrates multi-omics data to predict breast cancer subtypes. Evaluation results show high accuracy and improved correlation with patient survival compared to existing methods.
Cancer subtyping delivers valuable insights into the study of cancer heterogeneity and fulfills an essential step toward personalized medicine. For example, studies in breast cancer have shown that cancer subtypes based on molecular differences are associated with different patient survival and treatment responses. However, recent studies have suggested inconsistent breast cancer subtype classifications using alternative approaches, suggesting that current methods are yet to be optimized. Existing computation-based methods have also been limited by their dependency on incomplete prior knowledge and ineffectiveness in handling high-dimensional data beyond gene expression. Here, we propose a novel deep-learning-based algorithm, Moanna, that is trained to integrate multi-omics data for predicting breast cancer subtypes. Moanna's architecture consists of a semi-supervised Autoencoder attached to a multi-task learning network for generalizing the combination of gene expression, copy number and somatic mutation data. We trained Moanna on a subset of the METABRIC breast cancer dataset and evaluated the performance on the remaining hold-out METABRIC samples and a fully independent cohort of TCGA samples. We evaluated our use of Autoencoder against other dimensionality reduction techniques and demonstrated its superiority in learning patterns associated with breast cancer subtypes. The overall Moanna model also achieved high accuracy in predicting samples' ER status (96%), differentiating basal-like samples (98%), and classifying samples into PAM50 subtypes (85%). Moreover, Moanna's predicted subtypes show a stronger correlation with patient survival when compared to the original PAM50 subtypes.

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