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Systematic Verification of Upstream Regulators of a Computable Cellular Proliferation Network Model on Non-Diseased Lung Cells Using a Dedicated Dataset
We recently constructed a computable cell proliferation network (CPN) model focused on lung tissue to unravel complex biological processes and their exposure-related perturbations from molecular profiling data. The CPN consists of edges and nodes representing upstream controllers of gene expression...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3733638/ https://www.ncbi.nlm.nih.gov/pubmed/23926424 http://dx.doi.org/10.4137/BBI.S12167 |
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author | Belcastro, Vincenzo Poussin, Carine Gebel, Stephan Mathis, Carole Schlage, Walter K. Lichtner, Rosemarie B. Quadt-Humme, Sibille Wagner, Sandra Hoeng, Julia Peitsch, Manuel C. |
author_facet | Belcastro, Vincenzo Poussin, Carine Gebel, Stephan Mathis, Carole Schlage, Walter K. Lichtner, Rosemarie B. Quadt-Humme, Sibille Wagner, Sandra Hoeng, Julia Peitsch, Manuel C. |
author_sort | Belcastro, Vincenzo |
collection | PubMed |
description | We recently constructed a computable cell proliferation network (CPN) model focused on lung tissue to unravel complex biological processes and their exposure-related perturbations from molecular profiling data. The CPN consists of edges and nodes representing upstream controllers of gene expression largely generated from transcriptomics datasets using Reverse Causal Reasoning (RCR). Here, we report an approach to biologically verify the correctness of upstream controller nodes using a specifically designed, independent lung cell proliferation dataset. Normal human bronchial epithelial cells were arrested at G1/S with a cell cycle inhibitor. Gene expression changes and cell proliferation were captured at different time points after release from inhibition. Gene set enrichment analysis demonstrated cell cycle response specificity via an overrepresentation of proliferation related gene sets. Coverage analysis of RCR-derived hypotheses returned statistical significance for cell cycle response specificity across the whole model as well as for the Growth Factor and Cell Cycle sub-network models. |
format | Online Article Text |
id | pubmed-3733638 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-37336382013-08-07 Systematic Verification of Upstream Regulators of a Computable Cellular Proliferation Network Model on Non-Diseased Lung Cells Using a Dedicated Dataset Belcastro, Vincenzo Poussin, Carine Gebel, Stephan Mathis, Carole Schlage, Walter K. Lichtner, Rosemarie B. Quadt-Humme, Sibille Wagner, Sandra Hoeng, Julia Peitsch, Manuel C. Bioinform Biol Insights Original Research We recently constructed a computable cell proliferation network (CPN) model focused on lung tissue to unravel complex biological processes and their exposure-related perturbations from molecular profiling data. The CPN consists of edges and nodes representing upstream controllers of gene expression largely generated from transcriptomics datasets using Reverse Causal Reasoning (RCR). Here, we report an approach to biologically verify the correctness of upstream controller nodes using a specifically designed, independent lung cell proliferation dataset. Normal human bronchial epithelial cells were arrested at G1/S with a cell cycle inhibitor. Gene expression changes and cell proliferation were captured at different time points after release from inhibition. Gene set enrichment analysis demonstrated cell cycle response specificity via an overrepresentation of proliferation related gene sets. Coverage analysis of RCR-derived hypotheses returned statistical significance for cell cycle response specificity across the whole model as well as for the Growth Factor and Cell Cycle sub-network models. Libertas Academica 2013-07-23 /pmc/articles/PMC3733638/ /pubmed/23926424 http://dx.doi.org/10.4137/BBI.S12167 Text en © 2013 the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article published under the Creative Commons CC-BY-NC 3.0 license. |
spellingShingle | Original Research Belcastro, Vincenzo Poussin, Carine Gebel, Stephan Mathis, Carole Schlage, Walter K. Lichtner, Rosemarie B. Quadt-Humme, Sibille Wagner, Sandra Hoeng, Julia Peitsch, Manuel C. Systematic Verification of Upstream Regulators of a Computable Cellular Proliferation Network Model on Non-Diseased Lung Cells Using a Dedicated Dataset |
title | Systematic Verification of Upstream Regulators of a Computable Cellular Proliferation Network Model on Non-Diseased Lung Cells Using a Dedicated Dataset |
title_full | Systematic Verification of Upstream Regulators of a Computable Cellular Proliferation Network Model on Non-Diseased Lung Cells Using a Dedicated Dataset |
title_fullStr | Systematic Verification of Upstream Regulators of a Computable Cellular Proliferation Network Model on Non-Diseased Lung Cells Using a Dedicated Dataset |
title_full_unstemmed | Systematic Verification of Upstream Regulators of a Computable Cellular Proliferation Network Model on Non-Diseased Lung Cells Using a Dedicated Dataset |
title_short | Systematic Verification of Upstream Regulators of a Computable Cellular Proliferation Network Model on Non-Diseased Lung Cells Using a Dedicated Dataset |
title_sort | systematic verification of upstream regulators of a computable cellular proliferation network model on non-diseased lung cells using a dedicated dataset |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3733638/ https://www.ncbi.nlm.nih.gov/pubmed/23926424 http://dx.doi.org/10.4137/BBI.S12167 |
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