Affiliations 

  • 1 Health and Biomedical Innovation, UniSA Clinical and Health Sciences, University of South Australia, Adelaide, 5000, Australia; Genome Health Foundation, North Brighton, SA, 5048, Australia; Universiti Kebangsaan Malaysia, 43600, Bangi, Selangor, Malaysia. Electronic address: mf.ghf@outlook.com
  • 2 Institute of Cancer Research, Department of Medicine I, Medical University of Vienna, Vienna, Austria
  • 3 Department of Public Health, University of Copenhagen, Denmark
  • 4 Laboratory for Cell Genetics, Department Biology, Faculty of Sciences and Bio-Engineering Sciences, Vrije Universiteit Brussel, Pleinlaan 2, 1050, Brussels, Belgium
  • 5 Health and Biomedical Innovation, UniSA Clinical and Health Sciences, University of South Australia, Adelaide, 5000, Australia
  • 6 University of Vienna, Research Platform Active Ageing, Department of Nutritional Sciences, Althanstraße 14, 1090, Vienna, Austria
  • 7 Institute of Pharmacology and Toxicology, University of Wuerzburg, Wuerzburg, Germany
  • 8 CNR Institute of Clinical Physiology, Via Moruzzi 1, Pisa, Italy
  • 9 Environmental Carcinogenesis Unit, Ospedale Policlinico San Martino, Genoa, Italy
  • 10 Universidade da Coruña, Grupo DICOMOSA, Centro de Investigaciones Científicas Avanzadas (CICA), Departamento de Psicología, Facultad de Ciencias de la Educación, Campus Elviña s/n, 15071 A, Coruña, Spain; Instituto de Investigacio'n Biome'dica de A Coruña (INIBIC), AE CICA-INIBIC, Oza, 15071 A, Coruña, Spain
  • 11 Unit of Clinical and Molecular Epidemiology, IRCSS San Raffaele Pisana, Rome, Italy; Department of Human Sciences and Quality of Life Promotion, San Raffaele University, Via di Val Cannuta, 247, 00166, Rome, Italy
Mutat Res Rev Mutat Res, 2021 06 05;788:108384.
PMID: 34893149 DOI: 10.1016/j.mrrev.2021.108384

Abstract

The purpose of the "Micronuclei and Disease" special issue (SI) is to: (i) Determine the level of evidence for association of micronuclei (MN), a biomarker of numerical and structural chromosomal aberrations, with risk of specific diseases in humans; (ii) Define plausible mechanisms that explain association of MN with each disease; (iii) Identify knowledge gaps and research needed to translate MN assays into clinical practice. The "MN and Disease" SI includes 14 papers. The first is a review of mechanisms of MN formation and their consequences in humans. 11 papers are systematic reviews and/or meta-analyses of the association of MN with reproduction, child health, inflammation, auto-immune disease, glycation, metabolic diseases, chronic kidney disease, cardiovascular disease, eleven common cancers, ageing and frailty. The penultimate paper focuses on effect of interventions on MN frequency in the elderly. A road map for translation of MN data into clinical practice is the topic of the final paper. The majority of reviewed studies were case-control studies in which the ratio of mean MN frequency in disease cases relative to controls, i.e. the mean ratio (MR), was calculated. The mean of these MR values, estimated by meta-analyses, for lymphocyte and buccal cell MN in non-cancer diseases were 2.3 and 3.6 respectively, and for cancers they were 1.7 and 2.6 respectively. The highest MR values were observed in studies of cancer cases in which MN were measured in the same tissue as the tumour (MR = 4.9-10.8). This special issue is an important milestone in the evidence supporting MN as a reliable genomic biomarker of developmental and degenerative disease risk. These advances, together with results from prospective cohort studies, are helping to identify diseases in which MN assays can be practically employed in the clinical setting to better identify high risk patients and to prioritise them for preventive therapy.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.