eTumorMetastasis: A Network-based Algorithm Predicts Clinical Outcomes Using Whole-exome Sequencing Data of Cancer Patients
Continual reduction in sequencing cost is expanding the accessibility of genome sequencing data for routine clinical applications. However, the lack of methods to construct machine learning-based predictive models using these datasets has become a crucial bottleneck for the application of sequencing...
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Abstract | Continual reduction in sequencing cost is expanding the accessibility of genome sequencing data for routine clinical applications. However, the lack of methods to construct machine learning-based predictive models using these datasets has become a crucial bottleneck for the application of sequencing technology in clinics. Here, we develop a new algorithm, eTumorMetastasis, which transforms tumor functional mutations into network-based profiles and identifies network operational gene (NOG) signatures. NOG signatures model the tipping point at which a tumor cell shifts from a state that doesn’t favor recurrence to one that does. We show that NOG signatures derived from genomic mutations of tumor founding clones (i.e., the ‘most recent common ancestor’ of the cells within a tumor) significantly distinguish the recurred and non-recurred breast tumors as well as outperform the most popular genomic test (i.e., Oncotype DX). These results imply that mutations of the tumor founding clones are associated with tumor recurrence and can be used to predict clinical outcomes. As such, predictive tools could be used in clinics to guide treatment routes. Finally, the concepts underlying the eTumorMetastasis pave the way for the application of genome sequencing in predictions for other complex genetic diseases. eTumorMetastasis pseudocode and related data used in this study are available at https://github.com/WangEdwinLab/eTumorMetastasis. |
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AbstractList | NRC publication: Yes Continual reduction in sequencing cost is expanding the accessibility of genome sequencing data for routine clinical applications. However, the lack of methods to construct machine learning -based predictive models using these datasets has become a crucial bottleneck for the application of sequencing technology in clinics. Here, we develop a new algorithm, eTumorMetastasis, which transforms tumor functional mutations into network-based profiles and identifies network operational gene (NOG) signatures. NOG signatures model the tipping point at which a tumor cell shifts from a state that doesn’t favor recurrence to one that does. We show that NOG signatures derived from genomic mutations of tumor founding clones ( i.e. , the ‘most recent common ancestor’ of the cells within a tumor) significantly distinguish the recurred and non-recurred breast tumors as well as outperform the most popular genomic test ( i.e. , Oncotype DX). These results imply that mutations of the tumor founding clones are associated with tumor recurrence and can be used to predict clinical outcomes. As such, predictive tools could be used in clinics to guide treatment routes. Finally, the concepts underlying the eTumorMetastasis pave the way for the application of genome sequencing in predictions for other complex genetic diseases. eTumorMetastasis pseudocode and related data used in this study are available at https://github.com/WangEdwinLab/eTumorMetastasis . Continual reduction in sequencing cost is expanding the accessibility of genome sequencing data for routine clinical applications. However, the lack of methods to construct machine learning-based predictive models using these datasets has become a crucial bottleneck for the application of sequencing technology in clinics. Here, we develop a new algorithm, eTumorMetastasis, which transforms tumor functional mutations into network-based profiles and identifies network operational gene (NOG) signatures. NOG signatures model the tipping point at which a tumor cell shifts from a state that doesn’t favor recurrence to one that does. We show that NOG signatures derived from genomic mutations of tumor founding clones (i.e., the ‘most recent common ancestor’ of the cells within a tumor) significantly distinguish the recurred and non-recurred breast tumors as well as outperform the most popular genomic test (i.e., Oncotype DX). These results imply that mutations of the tumor founding clones are associated with tumor recurrence and can be used to predict clinical outcomes. As such, predictive tools could be used in clinics to guide treatment routes. Finally, the concepts underlying the eTumorMetastasis pave the way for the application of genome sequencing in predictions for other complex genetic diseases. eTumorMetastasis pseudocode and related data used in this study are available at https://github.com/WangEdwinLab/eTumorMetastasis. Continual reduction in sequencing cost is expanding the accessibility of genome sequencing data for routine clinical applications. However, the lack of methods to construct machine learning-based predictive models using these datasets has become a crucial bottleneck for the application of sequencing technology in clinics. Here we developed a new algorithm, eTumorMetastasis, which transforms tumor functional mutations into network-based profiles and identifies network operational gene signatures (NOG signatures). NOG signatures model the tipping point at which a tumor cell shifts from a state that doesn't favor recurrence to one that does. We showed that NOG signatures derived from genomic mutations of tumor founding clones (i.e., the 'most recent common ancestor' of the cells within a tumor) significantly distinguished recurred and non-recurred breast tumors as well as outperformed the most popular genomic test (i.e., Oncotype DX breast cancer recurrence score). These results imply that mutations of the tumor founding clones are associated with tumor recurrence and can be used to predict clinical outcomes. As such, predictive tools could be used in clinics to guide treatment routes. Finally, the concepts underlying the eTumorMetastasis pave the way for the application of genome sequencing in predictions for other complex genetic diseases. ETumorMetastasis pseudocode and related data used in this study can be found in our Github directory (https://github.com/WangEdwinLab/eTumorMetastasis). |
Author | Meng, Zhigang Wang, Edwin Tibiche, Chabane Droit, Arnaud Milanese, Jean-Sébastien Zou, Jinfeng Zaman, Naif Nantel, Andre Han, Pengyong |
AuthorAffiliation | Human Health Therapeutics,National Research Council Canada,Montreal H4P 2R2,Canada;Genomics Center,Centre Hospitalier Universitaire de Québec-UniversitéLaval Research Center,Quebec G1V 4G2,Canada%Human Health Therapeutics,National Research Council Canada,Montreal H4P 2R2,Canada%Department of Biochemistry&Molecular Biology,Medical Genetics,and Oncology,University of Calgary,Calgary T2N 4N1,Canada%Department of Biochemistry&Molecular Biology,Medical Genetics,and Oncology,University of Calgary,Calgary T2N 4N1,Canada;Institute of Biotechnology,Chinese Academy of Agricultural Sciences,Beijing 100086,China%Genomics Center,Centre Hospitalier Universitaire de Québec-UniversitéLaval Research Center,Quebec G1V 4G2,Canada%Human Health Therapeutics,National Research Council Canada,Montreal H4P 2R2,Canada;Department of Biochemistry&Molecular Biology,Medical Genetics,and Oncology,University of Calgary,Calgary T2N 4N1,Canada;Alberta Children's Hospital Research Institute and Arnie Charbonneau Cancer |
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Keywords | Breast cancer Sequencing data Systems biology Predictive model Machine learning Predictive models System biology |
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Publisher | Elsevier B.V Elsevier Department of Medicine,McGill University,Montreal H3G 2M1,Canada Genomics Center,Centre Hospitalier Universitaire de Québec-UniversitéLaval Research Center,Quebec G1V 4G2,Canada%Human Health Therapeutics,National Research Council Canada,Montreal H4P 2R2,Canada%Department of Biochemistry&Molecular Biology,Medical Genetics,and Oncology,University of Calgary,Calgary T2N 4N1,Canada%Department of Biochemistry&Molecular Biology,Medical Genetics,and Oncology,University of Calgary,Calgary T2N 4N1,Canada Human Health Therapeutics,National Research Council Canada,Montreal H4P 2R2,Canada Department of Biochemistry&Molecular Biology,Medical Genetics,and Oncology,University of Calgary,Calgary T2N 4N1,Canada Institute of Biotechnology,Chinese Academy of Agricultural Sciences,Beijing 100086,China%Genomics Center,Centre Hospitalier Universitaire de Québec-UniversitéLaval Research Center,Quebec G1V 4G2,Canada%Human Health Therapeutics,National Research Council Canada,Montreal H4P 2R2,Canada Alberta Children's Hospital Research Institute and Arnie Charbonneau Cancer Research Institute,University of Calgary,Calgary T2N 4N1,Canada |
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SubjectTerms | algorithms ancestry bioinformatics Breast cancer breast neoplasms breasts cancer recurrence data collection genes genomics Machine learning neoplasm cells Original Research Predictive model proteomics Sequencing data Systems biology |
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Title | eTumorMetastasis: A Network-based Algorithm Predicts Clinical Outcomes Using Whole-exome Sequencing Data of Cancer Patients |
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