TY - JOUR
T1 - Micronuclei and disease – Report of HUMN project workshop at Rennes 2019 EEMGS conference
AU - Fenech, Michael
AU - Holland, Nina
AU - Kirsch-Volders, Micheline
AU - Knudsen, Lisbeth E.
AU - Wagner, Karl Heinz
AU - Stopper, Helga
AU - Knasmueller, Siegfried
AU - Bolognesi, Claudia
AU - El-Zein, Randa
AU - Bonassi, Stefano
N1 - Funding Information:
The HUMN project is thankful for the support that European Environmental Mutagen and Genomics Society provided by hosting the workshop and specifically to Ludovic Le Hegarat and Sophie Langouet who enabled this possibility. The workshop was sponsored by MetaSystems (https://metasystems-international.com/) and ASELL (https://asell-llc.com/) which are private companies that develop and sell technologies and instruments for automated scoring of micronuclei. We would also like to acknowledge all the researchers and study participants without whom the reported knowledge on the association of MN with disease could not have been achieved.
Publisher Copyright:
© 2020 Elsevier B.V.
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/2/1
Y1 - 2020/2/1
N2 - The “Micronuclei and Disease” workshop was organized by the HUMN Project consortium and hosted by the European Environmental Mutagen and Genomics Society at their annual meeting in Rennes, France, on 23 May 2019. The program of the workshop focused on addressing the emerging evidence linking micronucleus (MN) frequency to human disease. The first objective was to review what has been published and evaluate the level and quality of evidence for the connection between MN frequency and various diseases through all life stages. The second objective was to identify the knowledge gaps and what else needs to be done to determine the clinical utility of MN assays as predictors of disease risk and of prognosis when disease is active. Speakers at the workshop discussed the association of MN frequency with inflammation, infertility, pregnancy complications, obesity, diabetes, cardiovascular disease, kidney disease, cervical and bladder cancer, oral head and neck cancer, lung cancer, accelerated ageing syndromes, neurodegenerative diseases, and a road-map on how to utilise this knowledge was proposed. The outcomes of the workshop indicated that there are significant opportunities for translating the application of MN assays into clinical practice to improve disease prevention and risk management and to inform public health policy.
AB - The “Micronuclei and Disease” workshop was organized by the HUMN Project consortium and hosted by the European Environmental Mutagen and Genomics Society at their annual meeting in Rennes, France, on 23 May 2019. The program of the workshop focused on addressing the emerging evidence linking micronucleus (MN) frequency to human disease. The first objective was to review what has been published and evaluate the level and quality of evidence for the connection between MN frequency and various diseases through all life stages. The second objective was to identify the knowledge gaps and what else needs to be done to determine the clinical utility of MN assays as predictors of disease risk and of prognosis when disease is active. Speakers at the workshop discussed the association of MN frequency with inflammation, infertility, pregnancy complications, obesity, diabetes, cardiovascular disease, kidney disease, cervical and bladder cancer, oral head and neck cancer, lung cancer, accelerated ageing syndromes, neurodegenerative diseases, and a road-map on how to utilise this knowledge was proposed. The outcomes of the workshop indicated that there are significant opportunities for translating the application of MN assays into clinical practice to improve disease prevention and risk management and to inform public health policy.
KW - Disease
KW - HUMN
KW - Micronuclei
KW - Micronucleus
KW - Report
KW - Workshop
KW - Micronucleus Tests
KW - Metagenomics
KW - Micronuclei, Chromosome-Defective/drug effects
KW - Humans
KW - DNA Damage/drug effects
KW - Mutagens/toxicity
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U2 - 10.1016/j.mrgentox.2020.503133
DO - 10.1016/j.mrgentox.2020.503133
M3 - Article
C2 - 32247551
AN - SCOPUS:85078444232
SN - 1383-5718
VL - 850-851
SP - 503133
JO - Mutation Research - Genetic Toxicology and Environmental Mutagenesis
JF - Mutation Research - Genetic Toxicology and Environmental Mutagenesis
M1 - 503133
ER -