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CDRgator: An Integrative Navigator of Cancer Drug Resistance Gene Signatures
Understanding the mechanisms of cancer drug resistance is a critical challenge in cancer therapy. For many cancer drugs, various resistance mechanisms have been identified such as target alteration, alternative signaling pathways, epithelial–mesenchymal transition, and epigenetic modulation. Resista...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Molecular and Cellular Biology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449719/ https://www.ncbi.nlm.nih.gov/pubmed/30759968 http://dx.doi.org/10.14348/molcells.2018.0413 |
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author | Jang, Su-Kyeong Yoon, Byung-Ha Kang, Seung Min Yoon, Yeo-Gha Kim, Seon-Young Kim, Wankyu |
author_facet | Jang, Su-Kyeong Yoon, Byung-Ha Kang, Seung Min Yoon, Yeo-Gha Kim, Seon-Young Kim, Wankyu |
author_sort | Jang, Su-Kyeong |
collection | PubMed |
description | Understanding the mechanisms of cancer drug resistance is a critical challenge in cancer therapy. For many cancer drugs, various resistance mechanisms have been identified such as target alteration, alternative signaling pathways, epithelial–mesenchymal transition, and epigenetic modulation. Resistance may arise via multiple mechanisms even for a single drug, making it necessary to investigate multiple independent models for comprehensive understanding and therapeutic application. In particular, we hypothesize that different resistance processes result in distinct gene expression changes. Here, we present a web-based database, CDRgator (Cancer Drug Resistance navigator) for comparative analysis of gene expression signatures of cancer drug resistance. Resistance signatures were extracted from two different types of datasets. First, resistance signatures were extracted from transcriptomic profiles of cancer cells or patient samples and their resistance-induced counterparts for >30 cancer drugs. Second, drug resistance group signatures were also extracted from two large-scale drug sensitivity datasets representing ~1,000 cancer cell lines. All the datasets are available for download, and are conveniently accessible based on drug class and cancer type, along with analytic features such as clustering analysis, multidimensional scaling, and pathway analysis. CDRgator allows meta-analysis of independent resistance models for more comprehensive understanding of drug-resistance mechanisms that is difficult to accomplish with individual datasets alone (database URL: http://cdrgator.ewha.ac.kr). |
format | Online Article Text |
id | pubmed-6449719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Society for Molecular and Cellular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-64497192019-04-10 CDRgator: An Integrative Navigator of Cancer Drug Resistance Gene Signatures Jang, Su-Kyeong Yoon, Byung-Ha Kang, Seung Min Yoon, Yeo-Gha Kim, Seon-Young Kim, Wankyu Mol Cells Article Understanding the mechanisms of cancer drug resistance is a critical challenge in cancer therapy. For many cancer drugs, various resistance mechanisms have been identified such as target alteration, alternative signaling pathways, epithelial–mesenchymal transition, and epigenetic modulation. Resistance may arise via multiple mechanisms even for a single drug, making it necessary to investigate multiple independent models for comprehensive understanding and therapeutic application. In particular, we hypothesize that different resistance processes result in distinct gene expression changes. Here, we present a web-based database, CDRgator (Cancer Drug Resistance navigator) for comparative analysis of gene expression signatures of cancer drug resistance. Resistance signatures were extracted from two different types of datasets. First, resistance signatures were extracted from transcriptomic profiles of cancer cells or patient samples and their resistance-induced counterparts for >30 cancer drugs. Second, drug resistance group signatures were also extracted from two large-scale drug sensitivity datasets representing ~1,000 cancer cell lines. All the datasets are available for download, and are conveniently accessible based on drug class and cancer type, along with analytic features such as clustering analysis, multidimensional scaling, and pathway analysis. CDRgator allows meta-analysis of independent resistance models for more comprehensive understanding of drug-resistance mechanisms that is difficult to accomplish with individual datasets alone (database URL: http://cdrgator.ewha.ac.kr). Korean Society for Molecular and Cellular Biology 2019-03-31 2019-02-12 /pmc/articles/PMC6449719/ /pubmed/30759968 http://dx.doi.org/10.14348/molcells.2018.0413 Text en © The Korean Society for Molecular and Cellular Biology. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/. |
spellingShingle | Article Jang, Su-Kyeong Yoon, Byung-Ha Kang, Seung Min Yoon, Yeo-Gha Kim, Seon-Young Kim, Wankyu CDRgator: An Integrative Navigator of Cancer Drug Resistance Gene Signatures |
title | CDRgator: An Integrative Navigator of Cancer Drug Resistance Gene Signatures |
title_full | CDRgator: An Integrative Navigator of Cancer Drug Resistance Gene Signatures |
title_fullStr | CDRgator: An Integrative Navigator of Cancer Drug Resistance Gene Signatures |
title_full_unstemmed | CDRgator: An Integrative Navigator of Cancer Drug Resistance Gene Signatures |
title_short | CDRgator: An Integrative Navigator of Cancer Drug Resistance Gene Signatures |
title_sort | cdrgator: an integrative navigator of cancer drug resistance gene signatures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449719/ https://www.ncbi.nlm.nih.gov/pubmed/30759968 http://dx.doi.org/10.14348/molcells.2018.0413 |
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