Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Jang, Su-Kyeong, Yoon, Byung-Ha, Kang, Seung Min, Yoon, Yeo-Gha, Kim, Seon-Young, Kim, Wankyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Molecular and Cellular Biology 2019
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
_version_ 1783408909215596544
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
work_keys_str_mv AT jangsukyeong cdrgatoranintegrativenavigatorofcancerdrugresistancegenesignatures
AT yoonbyungha cdrgatoranintegrativenavigatorofcancerdrugresistancegenesignatures
AT kangseungmin cdrgatoranintegrativenavigatorofcancerdrugresistancegenesignatures
AT yoonyeogha cdrgatoranintegrativenavigatorofcancerdrugresistancegenesignatures
AT kimseonyoung cdrgatoranintegrativenavigatorofcancerdrugresistancegenesignatures
AT kimwankyu cdrgatoranintegrativenavigatorofcancerdrugresistancegenesignatures