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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.
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.
Affiliation
  • Vlaanderen J; Institute for Risk Assessment Sciences (IRAS), Utrecht University, Utrecht, The Netherlands.
  • Leenders M; Institute for Risk Assessment Sciences (IRAS), Utrecht University, Utrecht, The Netherlands.
  • Chadeau-Hyam M; Institute for Risk Assessment Sciences (IRAS), Utrecht University, Utrecht, The Netherlands.
  • Portengen L; Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK.
  • Kyrtopoulos SA; Institute for Risk Assessment Sciences (IRAS), Utrecht University, Utrecht, The Netherlands.
  • Bergdahl IA; Institute of Biology, Medicinal Chemistry and Biotechnology, National Hellenic Research Foundation, Athens, Greece.
  • Johansson AS; Department of Biobank Research, University of Umeå, Umeå, Sweden.
  • Hebels DD; Department of Oncology, University of Umeå, Umeå, Sweden.
  • de Kok TM; Department of Toxicogenomics, Maastricht University, Maastricht, The Netherlands.
  • Vineis P; Department of Toxicogenomics, Maastricht University, Maastricht, The Netherlands.
  • Vermeulen RC; Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK.
BMC Genomics ; 18(1): 239, 2017 03 20.
Article in En | MEDLINE | ID: mdl-28320322
ABSTRACT

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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Lymphocytic, Chronic, B-Cell / Biomarkers, Tumor / Transcriptome Type of study: Prognostic_studies Limits: Humans Language: En Journal: BMC Genomics Journal subject: GENETICA Year: 2017 Document type: Article Affiliation country: Países Bajos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Leukemia, Lymphocytic, Chronic, B-Cell / Biomarkers, Tumor / Transcriptome Type of study: Prognostic_studies Limits: Humans Language: En Journal: BMC Genomics Journal subject: GENETICA Year: 2017 Document type: Article Affiliation country: Países Bajos