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Evolution‐informed modeling improves outcome prediction for cancers
Despite wide applications of high‐throughput biotechnologies in cancer research, many biomarkers discovered by exploring large‐scale omics data do not provide satisfactory performance when used to predict cancer treatment outcomes. This problem is partly due to the overlooking of functional implicat...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5192825/ https://www.ncbi.nlm.nih.gov/pubmed/28035236 http://dx.doi.org/10.1111/eva.12417 |
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author | Liu, Li Chang, Yung Yang, Tao Noren, David P Long, Byron Kornblau, Steven Qutub, Amina Ye, Jieping |
author_facet | Liu, Li Chang, Yung Yang, Tao Noren, David P Long, Byron Kornblau, Steven Qutub, Amina Ye, Jieping |
author_sort | Liu, Li |
collection | PubMed |
description | Despite wide applications of high‐throughput biotechnologies in cancer research, many biomarkers discovered by exploring large‐scale omics data do not provide satisfactory performance when used to predict cancer treatment outcomes. This problem is partly due to the overlooking of functional implications of molecular markers. Here, we present a novel computational method that uses evolutionary conservation as prior knowledge to discover bona fide biomarkers. Evolutionary selection at the molecular level is nature's test on functional consequences of genetic elements. By prioritizing genes that show significant statistical association and high functional impact, our new method reduces the chances of including spurious markers in the predictive model. When applied to predicting therapeutic responses for patients with acute myeloid leukemia and to predicting metastasis for patients with prostate cancers, the new method gave rise to evolution‐informed models that enjoyed low complexity and high accuracy. The identified genetic markers also have significant implications in tumor progression and embrace potential drug targets. Because evolutionary conservation can be estimated as a gene‐specific, position‐specific, or allele‐specific parameter on the nucleotide level and on the protein level, this new method can be extended to apply to miscellaneous “omics” data to accelerate biomarker discoveries. |
format | Online Article Text |
id | pubmed-5192825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-51928252016-12-29 Evolution‐informed modeling improves outcome prediction for cancers Liu, Li Chang, Yung Yang, Tao Noren, David P Long, Byron Kornblau, Steven Qutub, Amina Ye, Jieping Evol Appl Original Articles Despite wide applications of high‐throughput biotechnologies in cancer research, many biomarkers discovered by exploring large‐scale omics data do not provide satisfactory performance when used to predict cancer treatment outcomes. This problem is partly due to the overlooking of functional implications of molecular markers. Here, we present a novel computational method that uses evolutionary conservation as prior knowledge to discover bona fide biomarkers. Evolutionary selection at the molecular level is nature's test on functional consequences of genetic elements. By prioritizing genes that show significant statistical association and high functional impact, our new method reduces the chances of including spurious markers in the predictive model. When applied to predicting therapeutic responses for patients with acute myeloid leukemia and to predicting metastasis for patients with prostate cancers, the new method gave rise to evolution‐informed models that enjoyed low complexity and high accuracy. The identified genetic markers also have significant implications in tumor progression and embrace potential drug targets. Because evolutionary conservation can be estimated as a gene‐specific, position‐specific, or allele‐specific parameter on the nucleotide level and on the protein level, this new method can be extended to apply to miscellaneous “omics” data to accelerate biomarker discoveries. John Wiley and Sons Inc. 2016-10-21 /pmc/articles/PMC5192825/ /pubmed/28035236 http://dx.doi.org/10.1111/eva.12417 Text en © 2016 The Authors. Evolutionary Applications published by John Wiley & Sons Ltd This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Liu, Li Chang, Yung Yang, Tao Noren, David P Long, Byron Kornblau, Steven Qutub, Amina Ye, Jieping Evolution‐informed modeling improves outcome prediction for cancers |
title | Evolution‐informed modeling improves outcome prediction for cancers |
title_full | Evolution‐informed modeling improves outcome prediction for cancers |
title_fullStr | Evolution‐informed modeling improves outcome prediction for cancers |
title_full_unstemmed | Evolution‐informed modeling improves outcome prediction for cancers |
title_short | Evolution‐informed modeling improves outcome prediction for cancers |
title_sort | evolution‐informed modeling improves outcome prediction for cancers |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5192825/ https://www.ncbi.nlm.nih.gov/pubmed/28035236 http://dx.doi.org/10.1111/eva.12417 |
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