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Determining and interpreting correlations in lipidomic networks found in glioblastoma cells
BACKGROUND: Intelligent and multitiered quantitative analysis of biological systems rapidly evolves to a key technique in studying biomolecular cancer aspects. Newly emerging advances in both measurement as well as bio-inspired computational techniques have facilitated the development of lipidomics...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2944140/ https://www.ncbi.nlm.nih.gov/pubmed/20819237 http://dx.doi.org/10.1186/1752-0509-4-126 |
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author | Görke, Robert Meyer-Bäse, Anke Wagner, Dorothea He, Huan Emmett, Mark R Conrad, Charles A |
author_facet | Görke, Robert Meyer-Bäse, Anke Wagner, Dorothea He, Huan Emmett, Mark R Conrad, Charles A |
author_sort | Görke, Robert |
collection | PubMed |
description | BACKGROUND: Intelligent and multitiered quantitative analysis of biological systems rapidly evolves to a key technique in studying biomolecular cancer aspects. Newly emerging advances in both measurement as well as bio-inspired computational techniques have facilitated the development of lipidomics technologies and offer an excellent opportunity to understand regulation at the molecular level in many diseases. RESULTS: We present computational approaches to study the response of glioblastoma U87 cells to gene- and chemo-therapy. To identify distinct biomarkers and differences in therapeutic outcomes, we develop a novel technique based on graph-clustering. This technique facilitates the exploration and visualization of co-regulations in glioblastoma lipid profiling data. We investigate the changes in the correlation networks for different therapies and study the success of novel gene therapies targeting aggressive glioblastoma. CONCLUSIONS: The novel computational paradigm provides unique "fingerprints" by revealing the intricate interactions at the lipidome level in glioblastoma U87 cells with induced apoptosis (programmed cell death) and thus opens a new window to biomedical frontiers. |
format | Text |
id | pubmed-2944140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29441402010-10-19 Determining and interpreting correlations in lipidomic networks found in glioblastoma cells Görke, Robert Meyer-Bäse, Anke Wagner, Dorothea He, Huan Emmett, Mark R Conrad, Charles A BMC Syst Biol Research Article BACKGROUND: Intelligent and multitiered quantitative analysis of biological systems rapidly evolves to a key technique in studying biomolecular cancer aspects. Newly emerging advances in both measurement as well as bio-inspired computational techniques have facilitated the development of lipidomics technologies and offer an excellent opportunity to understand regulation at the molecular level in many diseases. RESULTS: We present computational approaches to study the response of glioblastoma U87 cells to gene- and chemo-therapy. To identify distinct biomarkers and differences in therapeutic outcomes, we develop a novel technique based on graph-clustering. This technique facilitates the exploration and visualization of co-regulations in glioblastoma lipid profiling data. We investigate the changes in the correlation networks for different therapies and study the success of novel gene therapies targeting aggressive glioblastoma. CONCLUSIONS: The novel computational paradigm provides unique "fingerprints" by revealing the intricate interactions at the lipidome level in glioblastoma U87 cells with induced apoptosis (programmed cell death) and thus opens a new window to biomedical frontiers. BioMed Central 2010-09-07 /pmc/articles/PMC2944140/ /pubmed/20819237 http://dx.doi.org/10.1186/1752-0509-4-126 Text en Copyright ©2010 Görke et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Görke, Robert Meyer-Bäse, Anke Wagner, Dorothea He, Huan Emmett, Mark R Conrad, Charles A Determining and interpreting correlations in lipidomic networks found in glioblastoma cells |
title | Determining and interpreting correlations in lipidomic networks found in glioblastoma cells |
title_full | Determining and interpreting correlations in lipidomic networks found in glioblastoma cells |
title_fullStr | Determining and interpreting correlations in lipidomic networks found in glioblastoma cells |
title_full_unstemmed | Determining and interpreting correlations in lipidomic networks found in glioblastoma cells |
title_short | Determining and interpreting correlations in lipidomic networks found in glioblastoma cells |
title_sort | determining and interpreting correlations in lipidomic networks found in glioblastoma cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2944140/ https://www.ncbi.nlm.nih.gov/pubmed/20819237 http://dx.doi.org/10.1186/1752-0509-4-126 |
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