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Genotypes of cancer stem cells characterized by epithelial-to-mesenchymal transition and proliferation related functions
Cancer stem cells (CSCs), or cancer cells with stem cell-like properties, generally exhibit drug resistance and have highly potent cancer inducing capabilities. Genome-wide expression data collected at public repositories over the last few years provide excellent material for studies that can lead t...
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/PMC5011650/ https://www.ncbi.nlm.nih.gov/pubmed/27597445 http://dx.doi.org/10.1038/srep32523 |
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author | Hsu, Chueh-Lin Chung, Feng-Hsiang Chen, Chih-Hao Hsu, Tzu-Ting Liu, Szu-Mam Chung, Dao-Sheng Hsu, Ya-Fen Chen, Chien-Lung Ma, Nianhan Lee, Hoong-Chien |
author_facet | Hsu, Chueh-Lin Chung, Feng-Hsiang Chen, Chih-Hao Hsu, Tzu-Ting Liu, Szu-Mam Chung, Dao-Sheng Hsu, Ya-Fen Chen, Chien-Lung Ma, Nianhan Lee, Hoong-Chien |
author_sort | Hsu, Chueh-Lin |
collection | PubMed |
description | Cancer stem cells (CSCs), or cancer cells with stem cell-like properties, generally exhibit drug resistance and have highly potent cancer inducing capabilities. Genome-wide expression data collected at public repositories over the last few years provide excellent material for studies that can lead to insights concerning the molecular and functional characteristics of CSCs. Here, we conducted functional genomic studies of CSC based on fourteen PCA-screened high quality public CSC whole genome gene expression datasets and, as control, four high quality non-stem-like cancer cell and non-cancerous stem cell datasets from the Gene Expression Omnibus database. A total of 6,002 molecular signatures were taken from the Molecular Signatures Database and used to characterize the datasets, which, under two-way hierarchical clustering, formed three genotypes. Type 1, consisting of mainly glia CSCs, had significantly enhanced proliferation, and significantly suppressed epithelial-mesenchymal transition (EMT), related functions. Type 2, mainly breast CSCs, had significantly enhanced EMT, but not proliferation, related functions. Type 3, composed of ovarian, prostate, and colon CSCs, had significantly suppressed proliferation related functions and mixed expressions on EMT related functions. |
format | Online Article Text |
id | pubmed-5011650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50116502016-09-12 Genotypes of cancer stem cells characterized by epithelial-to-mesenchymal transition and proliferation related functions Hsu, Chueh-Lin Chung, Feng-Hsiang Chen, Chih-Hao Hsu, Tzu-Ting Liu, Szu-Mam Chung, Dao-Sheng Hsu, Ya-Fen Chen, Chien-Lung Ma, Nianhan Lee, Hoong-Chien Sci Rep Article Cancer stem cells (CSCs), or cancer cells with stem cell-like properties, generally exhibit drug resistance and have highly potent cancer inducing capabilities. Genome-wide expression data collected at public repositories over the last few years provide excellent material for studies that can lead to insights concerning the molecular and functional characteristics of CSCs. Here, we conducted functional genomic studies of CSC based on fourteen PCA-screened high quality public CSC whole genome gene expression datasets and, as control, four high quality non-stem-like cancer cell and non-cancerous stem cell datasets from the Gene Expression Omnibus database. A total of 6,002 molecular signatures were taken from the Molecular Signatures Database and used to characterize the datasets, which, under two-way hierarchical clustering, formed three genotypes. Type 1, consisting of mainly glia CSCs, had significantly enhanced proliferation, and significantly suppressed epithelial-mesenchymal transition (EMT), related functions. Type 2, mainly breast CSCs, had significantly enhanced EMT, but not proliferation, related functions. Type 3, composed of ovarian, prostate, and colon CSCs, had significantly suppressed proliferation related functions and mixed expressions on EMT related functions. Nature Publishing Group 2016-09-06 /pmc/articles/PMC5011650/ /pubmed/27597445 http://dx.doi.org/10.1038/srep32523 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 Hsu, Chueh-Lin Chung, Feng-Hsiang Chen, Chih-Hao Hsu, Tzu-Ting Liu, Szu-Mam Chung, Dao-Sheng Hsu, Ya-Fen Chen, Chien-Lung Ma, Nianhan Lee, Hoong-Chien Genotypes of cancer stem cells characterized by epithelial-to-mesenchymal transition and proliferation related functions |
title | Genotypes of cancer stem cells characterized by epithelial-to-mesenchymal transition and proliferation related functions |
title_full | Genotypes of cancer stem cells characterized by epithelial-to-mesenchymal transition and proliferation related functions |
title_fullStr | Genotypes of cancer stem cells characterized by epithelial-to-mesenchymal transition and proliferation related functions |
title_full_unstemmed | Genotypes of cancer stem cells characterized by epithelial-to-mesenchymal transition and proliferation related functions |
title_short | Genotypes of cancer stem cells characterized by epithelial-to-mesenchymal transition and proliferation related functions |
title_sort | genotypes of cancer stem cells characterized by epithelial-to-mesenchymal transition and proliferation related functions |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5011650/ https://www.ncbi.nlm.nih.gov/pubmed/27597445 http://dx.doi.org/10.1038/srep32523 |
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