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Inferences of drug responses in cancer cells from cancer genomic features and compound chemical and therapeutic properties
Accurately predicting the response of a cancer patient to a therapeutic agent is a core goal of precision medicine. Existing approaches were mainly relied primarily on genomic alterations in cancer cells that have been treated with different drugs. Here we focus on predicting drug response based on...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028846/ https://www.ncbi.nlm.nih.gov/pubmed/27645580 http://dx.doi.org/10.1038/srep32679 |
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author | Wang, Yongcui Fang, Jianwen Chen, Shilong |
author_facet | Wang, Yongcui Fang, Jianwen Chen, Shilong |
author_sort | Wang, Yongcui |
collection | PubMed |
description | Accurately predicting the response of a cancer patient to a therapeutic agent is a core goal of precision medicine. Existing approaches were mainly relied primarily on genomic alterations in cancer cells that have been treated with different drugs. Here we focus on predicting drug response based on integration of the heterogeneously pharmacogenomics data from both cell and drug sides. Through a systematical approach, named as PDRCC (Predict Drug Response in Cancer Cells), the cancer genomic alterations and compound chemical and therapeutic properties were incorporated to determine the chemotherapeutic response in cancer patients. Using the Cancer Cell Line Encyclopedia (CCLE) study as the benchmark dataset, all pharmacogenomics data exhibited their roles in inferring the relationships between cancer cells and drugs. When integrating both genomic resources and compound information, the prediction coverage was significantly increased. The validity of PDRCC was also supported by its effective in uncovering the unknown cell-drug associations with database and literature evidences. It set the stage for clinical testing of novel therapeutic strategies, such as the sensitive association between cancer cell ‘A549_LUNG’ and compound ‘Topotecan’. In conclusion, PDRCC offers the possibility for faster, safer, and cheaper the development of novel anti-cancer therapeutics in the early-stage clinical trails. |
format | Online Article Text |
id | pubmed-5028846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50288462016-09-28 Inferences of drug responses in cancer cells from cancer genomic features and compound chemical and therapeutic properties Wang, Yongcui Fang, Jianwen Chen, Shilong Sci Rep Article Accurately predicting the response of a cancer patient to a therapeutic agent is a core goal of precision medicine. Existing approaches were mainly relied primarily on genomic alterations in cancer cells that have been treated with different drugs. Here we focus on predicting drug response based on integration of the heterogeneously pharmacogenomics data from both cell and drug sides. Through a systematical approach, named as PDRCC (Predict Drug Response in Cancer Cells), the cancer genomic alterations and compound chemical and therapeutic properties were incorporated to determine the chemotherapeutic response in cancer patients. Using the Cancer Cell Line Encyclopedia (CCLE) study as the benchmark dataset, all pharmacogenomics data exhibited their roles in inferring the relationships between cancer cells and drugs. When integrating both genomic resources and compound information, the prediction coverage was significantly increased. The validity of PDRCC was also supported by its effective in uncovering the unknown cell-drug associations with database and literature evidences. It set the stage for clinical testing of novel therapeutic strategies, such as the sensitive association between cancer cell ‘A549_LUNG’ and compound ‘Topotecan’. In conclusion, PDRCC offers the possibility for faster, safer, and cheaper the development of novel anti-cancer therapeutics in the early-stage clinical trails. Nature Publishing Group 2016-09-20 /pmc/articles/PMC5028846/ /pubmed/27645580 http://dx.doi.org/10.1038/srep32679 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Wang, Yongcui Fang, Jianwen Chen, Shilong Inferences of drug responses in cancer cells from cancer genomic features and compound chemical and therapeutic properties |
title | Inferences of drug responses in cancer cells from cancer genomic features and compound chemical and therapeutic properties |
title_full | Inferences of drug responses in cancer cells from cancer genomic features and compound chemical and therapeutic properties |
title_fullStr | Inferences of drug responses in cancer cells from cancer genomic features and compound chemical and therapeutic properties |
title_full_unstemmed | Inferences of drug responses in cancer cells from cancer genomic features and compound chemical and therapeutic properties |
title_short | Inferences of drug responses in cancer cells from cancer genomic features and compound chemical and therapeutic properties |
title_sort | inferences of drug responses in cancer cells from cancer genomic features and compound chemical and therapeutic properties |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5028846/ https://www.ncbi.nlm.nih.gov/pubmed/27645580 http://dx.doi.org/10.1038/srep32679 |
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