Identification of Sex-Specific Transcriptome Responses to Polychlorinated Biphenyls (PCBs)

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作者
Almudena Espín-Pérez
Dennie G. A. J. Hebels
Hannu Kiviranta
Panu Rantakokko
Panagiotis Georgiadis
Maria Botsivali
Ingvar A. Bergdahl
Domenico Palli
Florentin Späth
Anders Johansson
Marc Chadeau-Hyam
Soterios A. Kyrtopoulos
Jos C. S. Kleinjans
Theo M. C. M. de Kok
机构
[1] Maastricht University,Department of Toxicogenomics
[2] Maastricht University,MERLN Institute for Technology
[3] National Institute for Health and Welfare,inspired Regenerative Medicine
[4] National Hellenic Research Foundation,Department of Health Protection, Chemicals and Health Unit
[5] Umeå University,Institute of Biology, Medicinal Chemistry and Biotechnology
[6] ISPO Cancer Prevention and Research Institute,Department of Biobank Research, and Occupational and Environmental Medicine
[7] School of Public Health,Molecular and Nutritional Epidemiology UnitI
[8] Imperial College London,Department of Epidemiology and Biostatistics
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摘要
PCBs are classified as xenoestrogens and carcinogens and their health risks may be sex-specific. To identify potential sex-specific responses to PCB-exposure we established gene expression profiles in a population study subdivided into females and males. Gene expression profiles were determined in a study population consisting of 512 subjects from the EnviroGenomarkers project, 217 subjects who developed lymphoma and 295 controls were selected in later life. We ran linear mixed models in order to find associations between gene expression and exposure to PCBs, while correcting for confounders, in particular distribution of white blood cells (WBC), as well as random effects. The analysis was subdivided according to sex and development of lymphoma in later life. The changes in gene expression as a result of exposure to the six studied PCB congeners were sex- and WBC type specific. The relatively large number of genes that are significantly associated with PCB-exposure in the female subpopulation already indicates different biological response mechanisms to PCBs between the two sexes. The interaction analysis between different PCBs and WBCs provides only a small overlap between sexes. In males, cancer-related pathways and in females immune system-related pathways are identified in association with PCBs and WBCs. Future lymphoma cases and controls for both sexes show different responses to the interaction of PCBs with WBCs, suggesting a role of the immune system in PCB-related cancer development.
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