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Molecular Integrative Clustering of Asian Gastric Cell Lines Revealed Two Distinct Chemosensitivity Clusters

Cell lines recapitulate cancer heterogeneity without the presence of interfering tissue found in primary tumor. Their heterogeneous characteristics are reflected in their multiple genetic abnormalities and variable responsiveness to drug treatments. In order to understand the heterogeneity observed...

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Autores principales: Choong, Meng Ling, Tan, Shan Ho, Tan, Tuan Zea, Manesh, Sravanthy, Ngo, Anna, Yong, Jacklyn W. Y., Yang, Henry He, Lee, May Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208810/
https://www.ncbi.nlm.nih.gov/pubmed/25343454
http://dx.doi.org/10.1371/journal.pone.0111146
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author Choong, Meng Ling
Tan, Shan Ho
Tan, Tuan Zea
Manesh, Sravanthy
Ngo, Anna
Yong, Jacklyn W. Y.
Yang, Henry He
Lee, May Ann
author_facet Choong, Meng Ling
Tan, Shan Ho
Tan, Tuan Zea
Manesh, Sravanthy
Ngo, Anna
Yong, Jacklyn W. Y.
Yang, Henry He
Lee, May Ann
author_sort Choong, Meng Ling
collection PubMed
description Cell lines recapitulate cancer heterogeneity without the presence of interfering tissue found in primary tumor. Their heterogeneous characteristics are reflected in their multiple genetic abnormalities and variable responsiveness to drug treatments. In order to understand the heterogeneity observed in Asian gastric cancers, we have performed array comparative genomic hybridization (aCGH) on 18 Asian gastric cell lines. Hierarchical clustering and single-sample Gene Set Enrichment Analysis were performed on the aCGH data together with public gene expression data of the same cell lines obtained from the Cancer Cell Line Encyclopedia. We found a large amount of genetic aberrations, with some cell lines having 13 fold more aberrations than others. Frequently mutated genes and cellular pathways are identified in these Asian gastric cell lines. The combined analyses of aCGH and expression data demonstrate correlation of gene copy number variations and expression profiles in human gastric cancer cells. The gastric cell lines can be grouped into 2 integrative clusters (ICs). Gastric cells in IC1 are enriched with gene associated with mitochondrial activities and oxidative phosphorylation while cells in IC2 are enriched with genes associated with cell signaling and transcription regulations. The two clusters of cell lines were shown to have distinct responsiveness towards several chemotherapeutics agents such as PI3 K and proteosome inhibitors. Our molecular integrative clustering provides insight into critical genes and pathways that may be responsible for the differences in survival in response to chemotherapy.
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spelling pubmed-42088102014-10-27 Molecular Integrative Clustering of Asian Gastric Cell Lines Revealed Two Distinct Chemosensitivity Clusters Choong, Meng Ling Tan, Shan Ho Tan, Tuan Zea Manesh, Sravanthy Ngo, Anna Yong, Jacklyn W. Y. Yang, Henry He Lee, May Ann PLoS One Research Article Cell lines recapitulate cancer heterogeneity without the presence of interfering tissue found in primary tumor. Their heterogeneous characteristics are reflected in their multiple genetic abnormalities and variable responsiveness to drug treatments. In order to understand the heterogeneity observed in Asian gastric cancers, we have performed array comparative genomic hybridization (aCGH) on 18 Asian gastric cell lines. Hierarchical clustering and single-sample Gene Set Enrichment Analysis were performed on the aCGH data together with public gene expression data of the same cell lines obtained from the Cancer Cell Line Encyclopedia. We found a large amount of genetic aberrations, with some cell lines having 13 fold more aberrations than others. Frequently mutated genes and cellular pathways are identified in these Asian gastric cell lines. The combined analyses of aCGH and expression data demonstrate correlation of gene copy number variations and expression profiles in human gastric cancer cells. The gastric cell lines can be grouped into 2 integrative clusters (ICs). Gastric cells in IC1 are enriched with gene associated with mitochondrial activities and oxidative phosphorylation while cells in IC2 are enriched with genes associated with cell signaling and transcription regulations. The two clusters of cell lines were shown to have distinct responsiveness towards several chemotherapeutics agents such as PI3 K and proteosome inhibitors. Our molecular integrative clustering provides insight into critical genes and pathways that may be responsible for the differences in survival in response to chemotherapy. Public Library of Science 2014-10-24 /pmc/articles/PMC4208810/ /pubmed/25343454 http://dx.doi.org/10.1371/journal.pone.0111146 Text en © 2014 Choong et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Choong, Meng Ling
Tan, Shan Ho
Tan, Tuan Zea
Manesh, Sravanthy
Ngo, Anna
Yong, Jacklyn W. Y.
Yang, Henry He
Lee, May Ann
Molecular Integrative Clustering of Asian Gastric Cell Lines Revealed Two Distinct Chemosensitivity Clusters
title Molecular Integrative Clustering of Asian Gastric Cell Lines Revealed Two Distinct Chemosensitivity Clusters
title_full Molecular Integrative Clustering of Asian Gastric Cell Lines Revealed Two Distinct Chemosensitivity Clusters
title_fullStr Molecular Integrative Clustering of Asian Gastric Cell Lines Revealed Two Distinct Chemosensitivity Clusters
title_full_unstemmed Molecular Integrative Clustering of Asian Gastric Cell Lines Revealed Two Distinct Chemosensitivity Clusters
title_short Molecular Integrative Clustering of Asian Gastric Cell Lines Revealed Two Distinct Chemosensitivity Clusters
title_sort molecular integrative clustering of asian gastric cell lines revealed two distinct chemosensitivity clusters
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208810/
https://www.ncbi.nlm.nih.gov/pubmed/25343454
http://dx.doi.org/10.1371/journal.pone.0111146
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