Development of diagnostic and prognostic molecular biomarkers in hepatocellular carcinoma using machine learning: A systematic review

Author:

Brar Amanpreet1,Zhu Alice1ORCID,Baciu Cristina2ORCID,Sharma Divya3,Xu Wei3,Orchanian‐Cheff Ani4ORCID,Wang Bo5,Reimand Jüri678,Grant Robert9,Bhat Mamatha210

Affiliation:

1. Department of Surgery University of Toronto Toronto Canada

2. Ajmera Transplant Program University Health Network, Toronto General Hospital Toronto Canada

3. Department of Biostatistics, Dalla Lana School of Public Health, Princess Margaret Cancer Centre University Health Network Toronto Ontario Canada

4. Library and Information Services University Health Network Toronto Ontario Canada

5. Vector Institute for Artificial Intelligence University of Toronto Toronto Canada

6. Computational Biology Program Ontario Institute for Cancer Research Toronto Canada

7. Department of Medical Biophysics University of Toronto Toronto Canada

8. Department of Molecular Genetics University of Toronto Toronto Canada

9. Department of Medical Oncology, Princess Margaret Cancer Centre University Health Network Toronto Ontario Canada

10. Division of Gastroenterology & Hepatology, Department of Medicine Temerty Faculty of Medicine, University of Toronto Toronto Canada

Abstract

AbstractHepatocellular carcinoma (HCC) is a leading cause of cancer‐related mortality and morbidity worldwide. Machine learning (ML) tools have been developed in recent years to generate diagnostic and prognostic molecular biomarkers for this high‐fatality cancer. To delineate the landscape of ML in HCC, we performed a systematic search of Ovid Medline, Ovid Embase, Cochrane Database of Systematic Reviews (Ovid) and Cochrane CENTRAL (Ovid) to identify studies of HCC molecular biomarkers using ML strategies. In total, 75 studies met our inclusion criteria, 53 of which were pertinent to diagnosis of HCC and 22 of which were pertinent to prognostication of HCC. Genomic, transcriptomic, epigenomic, proteomic and metabolomic signatures were derived using various ML techniques (supervised, unsupervised and deep learning approaches) using serum, urine and tissue samples of HCC. The ML algorithms achieved a sensitivity of up to 95% for the diagnosis of HCC. Through pathway analysis of the signatures derived by ML tools, we identified regulators of epithelial‐mesenchymal transition and the cancer pathway Ras/Raf/MAPK as being particularly prognostic of HCC outcome. The application of ML to molecular data in HCC has thus far resulted in the generation of highly sensitive diagnostic and prognostic signatures. In future, development of ML algorithms that incorporate clinical, laboratory, alongside molecular features will be needed to fulfil the promise of personalized HCC diagnosis and treatment.

Funder

Toronto General and Western Hospital Foundation

Publisher

Wiley

Subject

Ocean Engineering

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