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High-throughput RNAi screen for essential genes and drug synergistic combinations in colorectal cancer
Metastatic colorectal cancer is a leading cause of cancer death. However, current therapy options are limited to chemotherapy, with the addition of anti-EGFR antibodies for patients with RAS wild-type tumours. Novel drug targets, or drug combinations that induce a synergistic response, would be of g...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625556/ https://www.ncbi.nlm.nih.gov/pubmed/28972570 http://dx.doi.org/10.1038/sdata.2017.139 |
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author | Williams, Steven P. Barthorpe, Andrew S. Lightfoot, Howard Garnett, Mathew J. McDermott, Ultan |
author_facet | Williams, Steven P. Barthorpe, Andrew S. Lightfoot, Howard Garnett, Mathew J. McDermott, Ultan |
author_sort | Williams, Steven P. |
collection | PubMed |
description | Metastatic colorectal cancer is a leading cause of cancer death. However, current therapy options are limited to chemotherapy, with the addition of anti-EGFR antibodies for patients with RAS wild-type tumours. Novel drug targets, or drug combinations that induce a synergistic response, would be of great benefit to patients. The identification of genes that are essential for cell survival can be undertaken using functional genomics screens. Furthermore, performing such screens in the presence of a targeted agent would allow the identification of combinations that result in a synthetic lethal interaction. Here, we present a dataset containing the results of a large scale RNAi screen (815 genes) to detect essential genes as well as synergistic combinations with targeted therapeutic agents using a panel of 27 colorectal cancer cell lines. These data identify genes that are essential for colorectal cancer cell survival as well as synthetic lethal treatment combinations using novel computational approaches. Moreover, this dataset could be utilised in combination with genomic profiling to identify predictive biomarkers of response. |
format | Online Article Text |
id | pubmed-5625556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-56255562017-10-04 High-throughput RNAi screen for essential genes and drug synergistic combinations in colorectal cancer Williams, Steven P. Barthorpe, Andrew S. Lightfoot, Howard Garnett, Mathew J. McDermott, Ultan Sci Data Data Descriptor Metastatic colorectal cancer is a leading cause of cancer death. However, current therapy options are limited to chemotherapy, with the addition of anti-EGFR antibodies for patients with RAS wild-type tumours. Novel drug targets, or drug combinations that induce a synergistic response, would be of great benefit to patients. The identification of genes that are essential for cell survival can be undertaken using functional genomics screens. Furthermore, performing such screens in the presence of a targeted agent would allow the identification of combinations that result in a synthetic lethal interaction. Here, we present a dataset containing the results of a large scale RNAi screen (815 genes) to detect essential genes as well as synergistic combinations with targeted therapeutic agents using a panel of 27 colorectal cancer cell lines. These data identify genes that are essential for colorectal cancer cell survival as well as synthetic lethal treatment combinations using novel computational approaches. Moreover, this dataset could be utilised in combination with genomic profiling to identify predictive biomarkers of response. Nature Publishing Group 2017-10-03 /pmc/articles/PMC5625556/ /pubmed/28972570 http://dx.doi.org/10.1038/sdata.2017.139 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ The Creative Commons Public Domain Dedication waiver http://creativecommons.org/publicdomain/zero/1.0/ applies to the metadata files made available in this article. |
spellingShingle | Data Descriptor Williams, Steven P. Barthorpe, Andrew S. Lightfoot, Howard Garnett, Mathew J. McDermott, Ultan High-throughput RNAi screen for essential genes and drug synergistic combinations in colorectal cancer |
title | High-throughput RNAi screen for essential genes and drug synergistic combinations in colorectal cancer |
title_full | High-throughput RNAi screen for essential genes and drug synergistic combinations in colorectal cancer |
title_fullStr | High-throughput RNAi screen for essential genes and drug synergistic combinations in colorectal cancer |
title_full_unstemmed | High-throughput RNAi screen for essential genes and drug synergistic combinations in colorectal cancer |
title_short | High-throughput RNAi screen for essential genes and drug synergistic combinations in colorectal cancer |
title_sort | high-throughput rnai screen for essential genes and drug synergistic combinations in colorectal cancer |
topic | Data Descriptor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5625556/ https://www.ncbi.nlm.nih.gov/pubmed/28972570 http://dx.doi.org/10.1038/sdata.2017.139 |
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