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Integrative analysis of cancer imaging readouts by networks

Cancer is a multifactorial and heterogeneous disease. The corresponding complexity appears at multiple levels: from the molecular and the cellular constitution to the macroscopic phenotype, and at the diagnostic and therapeutic management stages. The overall complexity can be approximated to a certa...

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Detalles Bibliográficos
Autores principales: Dominietto, Marco, Tsinoremas, Nicholas, Capobianco, Enrico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5528685/
https://www.ncbi.nlm.nih.gov/pubmed/25263240
http://dx.doi.org/10.1016/j.molonc.2014.08.013
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author Dominietto, Marco
Tsinoremas, Nicholas
Capobianco, Enrico
author_facet Dominietto, Marco
Tsinoremas, Nicholas
Capobianco, Enrico
author_sort Dominietto, Marco
collection PubMed
description Cancer is a multifactorial and heterogeneous disease. The corresponding complexity appears at multiple levels: from the molecular and the cellular constitution to the macroscopic phenotype, and at the diagnostic and therapeutic management stages. The overall complexity can be approximated to a certain extent, e.g. characterized by a set of quantitative phenotypic observables recorded in time‐space resolved dimensions by using multimodal imaging approaches. The transition from measures to data can be made effective through various computational inference methods, including networks, which are inherently capable of mapping variables and data to node‐ and/or edge‐valued topological properties, dynamic modularity configurations, and functional motifs. We illustrate how networks can integrate imaging data to explain cancer complexity, and assess potential pre‐clinical and clinical impact.
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spelling pubmed-55286852017-08-15 Integrative analysis of cancer imaging readouts by networks Dominietto, Marco Tsinoremas, Nicholas Capobianco, Enrico Mol Oncol Review Cancer is a multifactorial and heterogeneous disease. The corresponding complexity appears at multiple levels: from the molecular and the cellular constitution to the macroscopic phenotype, and at the diagnostic and therapeutic management stages. The overall complexity can be approximated to a certain extent, e.g. characterized by a set of quantitative phenotypic observables recorded in time‐space resolved dimensions by using multimodal imaging approaches. The transition from measures to data can be made effective through various computational inference methods, including networks, which are inherently capable of mapping variables and data to node‐ and/or edge‐valued topological properties, dynamic modularity configurations, and functional motifs. We illustrate how networks can integrate imaging data to explain cancer complexity, and assess potential pre‐clinical and clinical impact. John Wiley and Sons Inc. 2014-09-10 2015-01 /pmc/articles/PMC5528685/ /pubmed/25263240 http://dx.doi.org/10.1016/j.molonc.2014.08.013 Text en © 2015 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/3.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Review
Dominietto, Marco
Tsinoremas, Nicholas
Capobianco, Enrico
Integrative analysis of cancer imaging readouts by networks
title Integrative analysis of cancer imaging readouts by networks
title_full Integrative analysis of cancer imaging readouts by networks
title_fullStr Integrative analysis of cancer imaging readouts by networks
title_full_unstemmed Integrative analysis of cancer imaging readouts by networks
title_short Integrative analysis of cancer imaging readouts by networks
title_sort integrative analysis of cancer imaging readouts by networks
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5528685/
https://www.ncbi.nlm.nih.gov/pubmed/25263240
http://dx.doi.org/10.1016/j.molonc.2014.08.013
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