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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Published inGenomics, proteomics & bioinformatics Vol. 19; no. 6; pp. 973 - 985
Main Authors Milanese, Jean-Sébastien, Tibiche, Chabane, Zaman, Naif, Zou, Jinfeng, Han, Pengyong, Meng, Zhigang, Nantel, Andre, Droit, Arnaud, Wang, Edwin
Format Journal Article
LanguageEnglish
Published China Elsevier B.V 01.12.2021
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
Subjects
Online AccessGet full text
ISSN1672-0229
2210-3244
DOI10.1016/j.gpb.2020.06.009

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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.
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
AuthorAffiliation_xml – name: 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 Research Institute,University of Calgary,Calgary T2N 4N1,Canada;Department of Medicine,McGill University,Montreal H3G 2M1,Canada
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Issue 6
Keywords Breast cancer
Sequencing data
Systems biology
Predictive model
Machine learning
Predictive models
System biology
Language English
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PublicationTitle Genomics, proteomics & bioinformatics
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PublicationYear 2021
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
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Alberta Children's Hospital Research Institute and Arnie Charbonneau Cancer Research Institute,University of Calgary,Calgary T2N 4N1,Canada
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Snippet Continual reduction in sequencing cost is expanding the accessibility of genome sequencing data for routine clinical applications. However, the lack of methods...
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...
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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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