Molecular mechanisms by Which in vivo exposure to exogenous chemical genotoxic agents can lead to micronucleus formation in lymphocytes in vivo and ex vivo in humans

被引:100
|
作者
Fenech, Michael [1 ]
Knasmueller, Siegfried [2 ]
Bolognesi, Claudia [3 ]
Bonassi, Stefano [4 ]
Holland, Nina [5 ]
Migliore, Lucia [6 ]
Palitti, Fabrizio [7 ]
Natarajan, Adayapalam T. [7 ]
Kirsch-Volders, Micheline [8 ]
机构
[1] CSIRO, Food & Nutr Flagship, Genome Hlth & Personalised Nutr Lab, Adelaide, SA 5000, Australia
[2] Med Univ Vienna, Ctr Comprehens Canc, Dept Med 1, Inst Canc Res, Borschkegasse 8a, A-1090 Vienna, Austria
[3] Azienda Osped Univ San Martino, IRCCS, Environm Carcinogenesis Unit, IST Ist Nazl Ric Cancro, Largo Rosanna Benzi 10, I-16132 Genoa, Italy
[4] IRCCS San Raffaele Pisana, Unit Clin & Mol Epidemiol, Rome, Italy
[5] Univ Calif Berkeley, Sch Publ Hlth, Berkeley, CA 94720 USA
[6] Univ Pisa, Dept Translat Res & New Technol Med & Surg, Pisa, Italy
[7] Univ Tuscia, Dept Ecol & Biol Sci, Via San Camillo de Lellis Snc, I-01100 Viterbo, Italy
[8] Free Univ Brussels VUB, Fac Sci & Bioengn, Lab Cell Genet, Pleinlaan 2, B-1050 Brussels, Belgium
关键词
Molecular; Mechanisms; Micronucleus; Lymphocytes; Exogenous; Chemical; Genotoxiris; Exposure; In vivo; Ex vivo; Humans; CHROMOSOMAL-ABERRATION PRODUCTION; TELOMERIC DNA-DAMAGE; CYTOME ASSAY; CELL-CYCLE; NUTRITIONAL-REQUIREMENTS; NEUROSPORA ENDONUCLEASE; CYTOSINE-ARABINOSIDE; MAMMALIAN-CELLS; EXCISION-REPAIR; WIL2-NS CELLS;
D O I
10.1016/j.mrrev.2016.04.008
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The purpose of this review is, to summarise current knowledge on the molecular mechanisms by which in vivo exposure to exogenous chemical genotoxinsin humans induces micronuclei (MNi) and other nuclear anomalies in lymphocytes in vivo and ex vivo after nuclear division in vitro. MNi originate from acentric chromosome fragments and/or whole chromosomes that are unable to engage with the mitotic spindle and/or fail to segregate properly to the daughter nuclei during anaphase. The lagging fragments or whole chromosomes are surrounded by membrane and become MNi. Acentric fragments are caused by failure of repair or mis-repair of DNA strand breaks which may be induced by chemicals that (i) damage the phosphodiester backbone of DNA, and/or (ii) inhibit the DNA damage response mechanisms or repair of DNA strand breaks and/or (iii) cause DNA replication stress due to DNA adduct or cross-link formation. MNi originating from lagging whole chromosomes may be induced by chemicals that cause defects in centromeres or the mitotic machinery. Mis-repair of chemically-induced DNA breaks may also cause formation of dicentric chromosomes and nucleoplasmic bridges (NPBs) between daughter nuclei in mitosis. NPBs may break and initiate recurring breakage-fusion-bridge cycles and chromosomal instability. The review also explores knowledge on (i) the routes by which lymphocytes in the human body may be exposed to genotoxic chemicals, (ii) kinetics of MNi expression in lymphocytes in vivo and ex vivo in the lymphocyte cytokinesis-block micronucleus (L-CBMN) assay and (iii) current evidence on the efficiency of the L-CBMN assay in detecting in vivo exposure to chemical genotoxins and its concordance with MNi expression in epithelial tissues. The review also identifies important knowledge gaps (e.g. effect of nanomaterials; interactions with nutritional deficiencies etc.) regarding mechanisms by which in vivo chemical genotoxin exposure may cause MNi formation in lymphocytes in vivo and ex vivo in lymphocytes. (C) 2016 Published by Elsevier B.V.
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页码:12 / 25
页数:14
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