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Morphological and molecular breast cancer profiling through explainable machine learning

Authors
Binder, AlexanderBockmayr, MichaelHagele, MiriamWienert, StephanHeim, DanielHellweg, KatharinaIshii, MasaruStenzinger, AlbrechtHocke, AndreasDenkert, CarstenMueller, Klaus-RobertKlauschen, Frederick
Issue Date
Apr-2021
Publisher
SPRINGERNATURE
Citation
NATURE MACHINE INTELLIGENCE, v.3, no.4, pp.355 - 366
Indexed
SCIE
SCOPUS
Journal Title
NATURE MACHINE INTELLIGENCE
Volume
3
Number
4
Start Page
355
End Page
366
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/128343
DOI
10.1038/s42256-021-00303-4
ISSN
2522-5839
Abstract
Recent advances in cancer research and diagnostics largely rely on new developments in microscopic or molecular profiling techniques, offering high levels of detail with respect to either spatial or molecular features, but usually not both. Here, we present an explainable machine-learning approach for the integrated profiling of morphological, molecular and clinical features from breast cancer histology. First, our approach allows for the robust detection of cancer cells and tumour-infiltrating lymphocytes in histological images, providing precise heatmap visualizations explaining the classifier decisions. Second, molecular features, including DNA methylation, gene expression, copy number variations, somatic mutations and proteins are predicted from histology. Molecular predictions reach balanced accuracies up to 78%, whereas accuracies of over 95% can be achieved for subgroups of patients. Finally, our explainable AI approach allows assessment of the link between morphological and molecular cancer properties. The resulting computational multiplex-histology analysis can help promote basic cancer research and precision medicine through an integrated diagnostic scoring of histological, clinical and molecular features. Cancers are complex diseases that are increasingly studied using a diverse set of omics data. At the same time, histological images show the interaction of cells, which is not visible with bulk omics methods. Binder and colleagues present a method to learn from both kinds of data, such that molecular markers can be associated with visible patterns in the tissue samples and be used for more accurate breast cancer diagnosis.
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