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Exploring the nature of prediagnostic blood transcriptome markers of chronic lymphocytic leukemia by assessing their overlap with the transcriptome at the clinical stage

BACKGROUND: We recently identified 700 genes whose expression levels were predictive of chronic lymphocytic leukemia (CLL) in a genome-wide gene expression analysis of prediagnostic blood from future cases and matched controls. We hypothesized that a large fraction of these markers were likely relat...

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Autores principales: Vlaanderen, Jelle, Leenders, Max, Chadeau-Hyam, Marc, Portengen, Lützen, Kyrtopoulos, Soterios A., Bergdahl, Ingvar A., Johansson, Ann-Sofie, Hebels, Dennie D.G.A.J., de Kok, Theo M.C.M., Vineis, Paolo, Vermeulen, Roel C.H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360061/
https://www.ncbi.nlm.nih.gov/pubmed/28320322
http://dx.doi.org/10.1186/s12864-017-3627-4
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author Vlaanderen, Jelle
Leenders, Max
Chadeau-Hyam, Marc
Portengen, Lützen
Kyrtopoulos, Soterios A.
Bergdahl, Ingvar A.
Johansson, Ann-Sofie
Hebels, Dennie D.G.A.J.
de Kok, Theo M.C.M.
Vineis, Paolo
Vermeulen, Roel C.H.
author_facet Vlaanderen, Jelle
Leenders, Max
Chadeau-Hyam, Marc
Portengen, Lützen
Kyrtopoulos, Soterios A.
Bergdahl, Ingvar A.
Johansson, Ann-Sofie
Hebels, Dennie D.G.A.J.
de Kok, Theo M.C.M.
Vineis, Paolo
Vermeulen, Roel C.H.
author_sort Vlaanderen, Jelle
collection PubMed
description BACKGROUND: We recently identified 700 genes whose expression levels were predictive of chronic lymphocytic leukemia (CLL) in a genome-wide gene expression analysis of prediagnostic blood from future cases and matched controls. We hypothesized that a large fraction of these markers were likely related to early disease manifestations. Here we aim to gain a better understanding of the natural history of the identified markers by comparing results from our prediagnostic analysis, the only prediagnostic analysis to date, to results obtained from a meta-analysis of a series of publically available transcriptomics profiles obtained in incident CLL cases and controls. RESULTS: We observed considerable overlap between the results from our prediagnostic study and the clinical CLL signals (p-value for overlap Bonferroni significant markers 0.01; p-value for overlap nominal significant markers < 2.20e-16). We observed similar patterns with time to diagnosis and similar functional annotations for the markers that were identified in both settings compared to the markers that were only identified in the prediagnostic study. These results suggest that both gene sets operate in similar pathways. CONCLUSION: An overlap exists between expression levels of genes predictive of CLL identified in prediagnostic blood and expression levels of genes associated to CLL at the clinical stage. Our analysis provides insight in a set of genes for which expression levels can be used to follow the time-course of the disease; providing an opportunity to study CLL progression in more detail in future studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3627-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-53600612017-03-24 Exploring the nature of prediagnostic blood transcriptome markers of chronic lymphocytic leukemia by assessing their overlap with the transcriptome at the clinical stage Vlaanderen, Jelle Leenders, Max Chadeau-Hyam, Marc Portengen, Lützen Kyrtopoulos, Soterios A. Bergdahl, Ingvar A. Johansson, Ann-Sofie Hebels, Dennie D.G.A.J. de Kok, Theo M.C.M. Vineis, Paolo Vermeulen, Roel C.H. BMC Genomics Research Article BACKGROUND: We recently identified 700 genes whose expression levels were predictive of chronic lymphocytic leukemia (CLL) in a genome-wide gene expression analysis of prediagnostic blood from future cases and matched controls. We hypothesized that a large fraction of these markers were likely related to early disease manifestations. Here we aim to gain a better understanding of the natural history of the identified markers by comparing results from our prediagnostic analysis, the only prediagnostic analysis to date, to results obtained from a meta-analysis of a series of publically available transcriptomics profiles obtained in incident CLL cases and controls. RESULTS: We observed considerable overlap between the results from our prediagnostic study and the clinical CLL signals (p-value for overlap Bonferroni significant markers 0.01; p-value for overlap nominal significant markers < 2.20e-16). We observed similar patterns with time to diagnosis and similar functional annotations for the markers that were identified in both settings compared to the markers that were only identified in the prediagnostic study. These results suggest that both gene sets operate in similar pathways. CONCLUSION: An overlap exists between expression levels of genes predictive of CLL identified in prediagnostic blood and expression levels of genes associated to CLL at the clinical stage. Our analysis provides insight in a set of genes for which expression levels can be used to follow the time-course of the disease; providing an opportunity to study CLL progression in more detail in future studies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-017-3627-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-20 /pmc/articles/PMC5360061/ /pubmed/28320322 http://dx.doi.org/10.1186/s12864-017-3627-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Vlaanderen, Jelle
Leenders, Max
Chadeau-Hyam, Marc
Portengen, Lützen
Kyrtopoulos, Soterios A.
Bergdahl, Ingvar A.
Johansson, Ann-Sofie
Hebels, Dennie D.G.A.J.
de Kok, Theo M.C.M.
Vineis, Paolo
Vermeulen, Roel C.H.
Exploring the nature of prediagnostic blood transcriptome markers of chronic lymphocytic leukemia by assessing their overlap with the transcriptome at the clinical stage
title Exploring the nature of prediagnostic blood transcriptome markers of chronic lymphocytic leukemia by assessing their overlap with the transcriptome at the clinical stage
title_full Exploring the nature of prediagnostic blood transcriptome markers of chronic lymphocytic leukemia by assessing their overlap with the transcriptome at the clinical stage
title_fullStr Exploring the nature of prediagnostic blood transcriptome markers of chronic lymphocytic leukemia by assessing their overlap with the transcriptome at the clinical stage
title_full_unstemmed Exploring the nature of prediagnostic blood transcriptome markers of chronic lymphocytic leukemia by assessing their overlap with the transcriptome at the clinical stage
title_short Exploring the nature of prediagnostic blood transcriptome markers of chronic lymphocytic leukemia by assessing their overlap with the transcriptome at the clinical stage
title_sort exploring the nature of prediagnostic blood transcriptome markers of chronic lymphocytic leukemia by assessing their overlap with the transcriptome at the clinical stage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360061/
https://www.ncbi.nlm.nih.gov/pubmed/28320322
http://dx.doi.org/10.1186/s12864-017-3627-4
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