TY - JOUR
T1 - microRNA expression profiles and personal monitoring of exposure to particulate matter
AU - Mancini, Francesca Romana
AU - Laine, Jessica E.
AU - Tarallo, Sonia
AU - Vlaanderen, Jelle
AU - Vermeulen, Roel
AU - van Nunen, Erik
AU - Hoek, Gerard
AU - Probst-Hensch, Nicole
AU - Imboden, Medea
AU - Jeong, Ayoung
AU - Gulliver, John
AU - Chadeau-Hyam, Marc
AU - Nieuwenhuijsen, Mark
AU - de Kok, Theo M.
AU - Piepers, Jolanda
AU - Krauskopf, Julian
AU - Kleinjans, Jos C. S.
AU - Vineis, Paolo
AU - Naccarati, Alessio
N1 - Funding Information:
Funded by the European Community - Seventh Framework Program ( FP7 /2007–2011 ) under grant agreement number: 308610 ( EXPOsOMICS ). This work also was supported by the Swiss National Science Foundation , SNF-SAPALDIA (grants number 33CS30-148470/1 ).
Funding Information:
Funded by the European Community - Seventh Framework Program (FP7/2007?2011) under grant agreement number: 308610 (EXPOsOMICS). This work also was supported by the Swiss National Science Foundation, SNF-SAPALDIA (grants number 33CS30-148470/1).
Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2020/8
Y1 - 2020/8
N2 - An increasing number of findings from epidemiological studies support associations between exposure to air pollution and the onset of several diseases, including pulmonary, cardiovascular and neurodegenerative diseases, and malignancies. However, intermediate, and potentially mediating, biological mechanisms associated with exposure to air pollutants are largely unknown. Previous studies on the human exposome have shown that the expression of certain circulating microRNAs (miRNAs), regulators of gene expression, are altered upon exposure to traffic-related air pollutants. In the present study, we investigated the relationship between particulate matter (PM) smaller than 2.5 mm (PM2.5), PM2.5 absorbance (as a proxy of black carbon and soot), and ultrafine-particles (UFP, smaller than 0.1 mm), measured in healthy volunteers by 24 h personal monitoring (PEM) sessions and global expression levels of peripheral blood miRNAs. The PEM sessions were conducted in four European countries, namely Switzerland (Basel), United Kingdom (Norwich), Italy (Turin), and The Netherlands (Utrecht). miRNAs expression levels were analysed using microarray technology on blood samples from 143 participants. Seven miRNAs, hsa-miR-24-3p, hsa-miR-4454, hsa-miR-4763-3p, hsa-miR-425-5p, hsa-let-7d-5p, hsa-miR502-5p, and hsa-miR-505-3p were significantly (FDR corrected) expressed in association with PM2.5 personal exposure, while no significant association was found between miRNA expression and the other pollutants. The results obtained from this investigation suggest that personal exposure to PM2.5 is associated with miRNA expression levels, showing the potential for these circulating miRNAs as novel biomarkers for air pollution health risk assessment. (C) 2020 Elsevier Ltd. All rights reserved.
AB - An increasing number of findings from epidemiological studies support associations between exposure to air pollution and the onset of several diseases, including pulmonary, cardiovascular and neurodegenerative diseases, and malignancies. However, intermediate, and potentially mediating, biological mechanisms associated with exposure to air pollutants are largely unknown. Previous studies on the human exposome have shown that the expression of certain circulating microRNAs (miRNAs), regulators of gene expression, are altered upon exposure to traffic-related air pollutants. In the present study, we investigated the relationship between particulate matter (PM) smaller than 2.5 mm (PM2.5), PM2.5 absorbance (as a proxy of black carbon and soot), and ultrafine-particles (UFP, smaller than 0.1 mm), measured in healthy volunteers by 24 h personal monitoring (PEM) sessions and global expression levels of peripheral blood miRNAs. The PEM sessions were conducted in four European countries, namely Switzerland (Basel), United Kingdom (Norwich), Italy (Turin), and The Netherlands (Utrecht). miRNAs expression levels were analysed using microarray technology on blood samples from 143 participants. Seven miRNAs, hsa-miR-24-3p, hsa-miR-4454, hsa-miR-4763-3p, hsa-miR-425-5p, hsa-let-7d-5p, hsa-miR502-5p, and hsa-miR-505-3p were significantly (FDR corrected) expressed in association with PM2.5 personal exposure, while no significant association was found between miRNA expression and the other pollutants. The results obtained from this investigation suggest that personal exposure to PM2.5 is associated with miRNA expression levels, showing the potential for these circulating miRNAs as novel biomarkers for air pollution health risk assessment. (C) 2020 Elsevier Ltd. All rights reserved.
KW - microRNAs
KW - Air pollution
KW - Fine and ultrafine particles
KW - Personal monitoring
KW - USE REGRESSION-MODELS
KW - AIR-POLLUTION
U2 - 10.1016/j.envpol.2020.114392
DO - 10.1016/j.envpol.2020.114392
M3 - Article
C2 - 32276129
SN - 0269-7491
VL - 263
JO - Environmental Pollution
JF - Environmental Pollution
M1 - 114392
ER -