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Transcriptomics in cancer revealed by Positron Emission Tomography radiomics

Metabolic images from Positron Emission Tomography (PET) are used routinely for diagnosis, follow-up or treatment planning purposes of cancer patients. In this study we aimed at determining if radiomic features extracted from (18)F-Fluoro Deoxy Glucose (FDG) PET images could mirror tumor transcripto...

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Autores principales: Tixier, Florent, Cheze-le-Rest, Catherine, Schick, Ulrike, Simon, Brigitte, Dufour, Xavier, Key, Stéphane, Pradier, Olivier, Aubry, Marc, Hatt, Mathieu, Corcos, Laurent, Visvikis, Dimitris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7101432/
https://www.ncbi.nlm.nih.gov/pubmed/32221360
http://dx.doi.org/10.1038/s41598-020-62414-z
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author Tixier, Florent
Cheze-le-Rest, Catherine
Schick, Ulrike
Simon, Brigitte
Dufour, Xavier
Key, Stéphane
Pradier, Olivier
Aubry, Marc
Hatt, Mathieu
Corcos, Laurent
Visvikis, Dimitris
author_facet Tixier, Florent
Cheze-le-Rest, Catherine
Schick, Ulrike
Simon, Brigitte
Dufour, Xavier
Key, Stéphane
Pradier, Olivier
Aubry, Marc
Hatt, Mathieu
Corcos, Laurent
Visvikis, Dimitris
author_sort Tixier, Florent
collection PubMed
description Metabolic images from Positron Emission Tomography (PET) are used routinely for diagnosis, follow-up or treatment planning purposes of cancer patients. In this study we aimed at determining if radiomic features extracted from (18)F-Fluoro Deoxy Glucose (FDG) PET images could mirror tumor transcriptomics. In this study we analyzed 45 patients with locally advanced head and neck cancer (H&N) that underwent FDG-PET scans at the time of diagnosis and transcriptome analysis using RNAs from both cancer and healthy tissues on microarrays. Association between PET radiomics and transcriptomics was carried out with the Genomica software and a functional annotation was used to associate PET radiomics, gene expression and altered biological pathways. We identified relationships between PET radiomics and genes involved in cell-cycle, disease, DNA repair, extracellular matrix organization, immune system, metabolism or signal transduction pathways, according to the Reactome classification. Our results suggest that these FDG PET radiomic features could be used to infer tissue gene expression and cellular pathway activity in H&N cancers. These observations strengthen the value of radiomics as a promising approach to personalize treatments through targeting tumor-specific molecular processes.
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spelling pubmed-71014322020-03-31 Transcriptomics in cancer revealed by Positron Emission Tomography radiomics Tixier, Florent Cheze-le-Rest, Catherine Schick, Ulrike Simon, Brigitte Dufour, Xavier Key, Stéphane Pradier, Olivier Aubry, Marc Hatt, Mathieu Corcos, Laurent Visvikis, Dimitris Sci Rep Article Metabolic images from Positron Emission Tomography (PET) are used routinely for diagnosis, follow-up or treatment planning purposes of cancer patients. In this study we aimed at determining if radiomic features extracted from (18)F-Fluoro Deoxy Glucose (FDG) PET images could mirror tumor transcriptomics. In this study we analyzed 45 patients with locally advanced head and neck cancer (H&N) that underwent FDG-PET scans at the time of diagnosis and transcriptome analysis using RNAs from both cancer and healthy tissues on microarrays. Association between PET radiomics and transcriptomics was carried out with the Genomica software and a functional annotation was used to associate PET radiomics, gene expression and altered biological pathways. We identified relationships between PET radiomics and genes involved in cell-cycle, disease, DNA repair, extracellular matrix organization, immune system, metabolism or signal transduction pathways, according to the Reactome classification. Our results suggest that these FDG PET radiomic features could be used to infer tissue gene expression and cellular pathway activity in H&N cancers. These observations strengthen the value of radiomics as a promising approach to personalize treatments through targeting tumor-specific molecular processes. Nature Publishing Group UK 2020-03-27 /pmc/articles/PMC7101432/ /pubmed/32221360 http://dx.doi.org/10.1038/s41598-020-62414-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tixier, Florent
Cheze-le-Rest, Catherine
Schick, Ulrike
Simon, Brigitte
Dufour, Xavier
Key, Stéphane
Pradier, Olivier
Aubry, Marc
Hatt, Mathieu
Corcos, Laurent
Visvikis, Dimitris
Transcriptomics in cancer revealed by Positron Emission Tomography radiomics
title Transcriptomics in cancer revealed by Positron Emission Tomography radiomics
title_full Transcriptomics in cancer revealed by Positron Emission Tomography radiomics
title_fullStr Transcriptomics in cancer revealed by Positron Emission Tomography radiomics
title_full_unstemmed Transcriptomics in cancer revealed by Positron Emission Tomography radiomics
title_short Transcriptomics in cancer revealed by Positron Emission Tomography radiomics
title_sort transcriptomics in cancer revealed by positron emission tomography radiomics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7101432/
https://www.ncbi.nlm.nih.gov/pubmed/32221360
http://dx.doi.org/10.1038/s41598-020-62414-z
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