Cytomic analysis: a modern universal tool for biomedical and ecological and hygienic research (literature review). Part 2
- Authors: Krivtsova E.K.1, Ingel F.I.1, Akhaltseva L.V.1
-
Affiliations:
- Centre for Strategic Planning and Management of Biomedical Health Risks of the Federal Medical Biological Agency
- Issue: Vol 100, No 11 (2021)
- Pages: 1333-1338
- Section: METHODS OF HYGIENIC AND EXPERIMENTAL INVESTIGATIONS
- Published: 06.12.2021
- URL: https://rjraap.com/0016-9900/article/view/638825
- DOI: https://doi.org/10.47470/0016-9900-2021-100-11-1333-1338
- ID: 638825
Cite item
Full Text
Abstract
In the second part of the review, examples of cytome analysis on both peripheral blood lymphocytes and human buccal epiteliocytes are given in the study of occupational risks and investigation of genome instabilities induced by alcohol and tobacco use. Much attention is paid to the cytome analysis application in environmental and hygienic research and the studies directed to evaluating natural and anthropogenic load to the human population, especially industrial, factors. The method of cytome analysis on primary culture of human peripheral blood lymphocytes cultivated with a cytokinetic block (CBMN-cyt test) in its current state is described in detail, and the history of its development is briefly reflected. The method of cytome analysis on human buccal epiteliocytes (BMN-cyt) is also analyzed. The review contains photomicrographs of genetic cell damages that are markers in micronuclei (MN) tests. We used PubMed, Web of Science, ResearchGate, Scopus, eLibrary databases as the sources of literature.
Contribution:
Krivtsova E.K. — search of literature sources, analysis and interpretation of literature data, writing a text;
Ingel F.I. — the concept and design of the study, a search of literature sources;
Akhaltseva L.V. — search of literature sources, analysis and interpretation of literature data.
All authors are responsible for the integrity of all parts of the manuscript and approval of the manuscript final version.
Conflict of interest. The authors declare no conflict of interest.
Acknowledgement. The study had no sponsorship.
Received: April 27, 2021 / Accepted: September 28, 2021 / Published: October 31, 2021
About the authors
Elena K. Krivtsova
Centre for Strategic Planning and Management of Biomedical Health Risks of the Federal Medical Biological Agency
Author for correspondence.
Email: ekrivcova@cspmz.ru
ORCID iD: 0000-0002-5039-8980
MD, researcher of the Department of Preventive Toxicology and Biomedical Research in the Centre for Strategic Planning of the Federal Medical Biological Agency, Moscow, 119121, Russian Federation.
e-mail: EKrivcova@cspmz.ru
Russian FederationFaina I. Ingel
Centre for Strategic Planning and Management of Biomedical Health Risks of the Federal Medical Biological Agency
Email: noemail@neicon.ru
ORCID iD: 0000-0002-2262-6800
Russian Federation
Lyudmila V. Akhaltseva
Centre for Strategic Planning and Management of Biomedical Health Risks of the Federal Medical Biological Agency
Email: noemail@neicon.ru
ORCID iD: 0000-0002-3619-3858
Russian Federation
References
- Lewinska D., Stepnik M., Krajewski W., Arkusz J., Stanczyk M., Wronska-Nofer T. Increased incidence of micronuclei assessed with the micronucleus assay and the Fluorescence in Situ Hybridization (FISH) technique in peripheral blood lymphocytes of nurses exposed to nitrous oxide. Mutat. Res. 2005; 581(102): 1–9. https://doi.org/10.1016/j.mrgentox.2004.10.018
- Cavallo D., Ursini C.L., Omodeo-Sale E., Iavicoli S. Micronucleus induction and FISH analysis in buccal cells and lymphocytes of nurses administering antineoplastic drugs. Mutat. Res. 2007; 628(1): 11–8. https://doi.org/10.1016/j.mrgentox.2006.10.014
- Kopjar N., Garaj-Vrhovac V., Kasuba V., Rozgaj R., Ramic S., Pavlica V., et al. Assessment of genotoxic risks in Croatian health care workers occupationally exposed to cytotoxic drugs: A multi-biomarker approach. Int. J. Hyg. Environ. Health. 2009; 212(4): 414–31. https://doi.org/10.1016/j.ijheh.2008.10.001
- Andreassi M.G. The biological effects of diagnostic cardiac imaging on chronically exposed physicians: the importance of being non-ionizing. Cardiovasc. Ultrasound. 2004; 2: 25. https://doi.org/10.1186/1476-7120-2-25
- Sahin A., Tatar A., Oztas S., Seven B., Varoglu E., Yesilyurt A., et al. Evaluation of the genotoxic effects of chronic low-dose ionizing radiation exposure on nuclear medicine workers. Nucl. Med. Biol. 2009; 36(5): 575–8. https://doi.org/10.1016/j.nucmedbio.2009.02.003
- Rohr P., da Silva J., da Silva F.R., Sarmento M., Porto C., Debastiani R., et al. Evaluation of genetic damage in open-cast coal mine workers using the buccal micronucleus cytome assay. Environ. Mol. Mutagen. 2013; 54(1): 65–71. https://doi.org/10.1002/em.21744
- Bruschweiler E.D., Hopf N.B., Wild P., Huynh C.K., Fenech M., Thomas P., et al. Workers exposed to wood dust have an increased micronucleus frequency in nasal and buccal cells: results from a pilot study. Mutagenesis. 2014; 29(3): 201–7. https://doi.org/10.1093/mutage/geu003
- Krishna L., Sampson U., Annamala P.T., Unni K.M., Binukumar B., George A., et al. Genomic instability in exfoliated buccal cells among cement warehouse workers. J. Occup. Environ. Med. 2020; 11(1): 33–40. https://doi.org/10.15171/ijoem.2020.1744
- Cobanoglu H., Coskun M., Coskun M., Cayir A. Results of buccal micronucleus cytome assay in pesticide-exposed and non-exposed group. Environ. Sci. Pollut. Res. Int. 2019; 26(19): 19676–83. https://doi.org/10.1007/s11356-019-05249-0
- Wultsch G., Nersesyan A., Kundi M., Jakse R., Beham A., Wagner K-H., et al. The sensitivity of biomarkers for genotoxicity and acute cytotoxicity in nasal and buccal cells of welders. Int. J. Hyg. Environ. Health. 2014; 217(4–5): 492–8. https://doi.org/10.1016/j.ijheh.2013.09.005
- Brina K.R., Carvalho T.S., Ardenghi P.G., da Silva L.B. Micronuclei and other nuclear anomalies in exfoliated buccal cells of urban solid waste collectors and recyclers in southern Brasil. Chemosphere. 2018; 193: 1058–62. https://doi.org/10.1016/j.chemosphere.2017.11.119
- Dash K.C., Nishat R., Kumar H., Mishra S., Raghuvanshi M., Bajoria A. Comparative study of micronuclei count in patients with different tobacco-related habits using exfoliated buccal epithelial cells: a tool for assessment of genotoxicity. J. Contemp. Dent. Pract. 2018; 19(9): 1076–81.
- Gopal K.S., Padma M. Evaluation of cytogenic damage in the form of micronuclei in oral exfoliated buccal cells in tobacco users. Indian J. Dent. Res. 2018; 29(6): 773–80. https://doi.org/10.4103/ijdr.IJDR_218_17
- Nefic H., Handzic I. The effect of age, sex, and lifestyle factors on micronucleus frequency in peripheral blood lymphocytes of the Bosnian population. Mutat Res. 2013; 753(1): 1–11. https://doi.org/10.1016/j.mrgentox.2013.03.001
- Haveric A., Haveric S., Ibrulj S. Micronuclei frequencies in peripheral blood and buccal exfoliated cells of young smokers and non-smokers. Toxicol. Mech. Methods. 2010; 20(5): 260–6. https://doi.org/10.3109/15376516.2010.482962
- Sordo M., Maciel-Ruiz J.A., Salazar A.M., Robles-Morales R., Veloz-Martinez M.G., Pacheco-Limon J.H., et al. Particulate matter-associated micronuclei frequencies in maternal and cord blood lymphocytes. Environ. Mol. Mutagen. 2019; 60(5): 421–7. https://doi.org/10.1002/em.22275
- Navasumrit P., Chaisatra K., Promvijit J., Parnlob V., Waraprasit S., Chompoobut C., et al. Exposure to arsenic in utero is associated with various types of DNA damage and micronuclei in newborns: a birth cohort study. Environ. Health. 2019; 18(1): 51. https://doi.org/10.1186/s12940-019-0481-7
- Marcon A.E., Navoni J.A., de Oliveira Galvao M.F., Garcia A.C.F.S., do Amaral V.C., Petta R.A., et al. Mutagenic potential assessment associated with human exposure to natural radioactivity. Chemosphere. 2017; 167: 36–43. https://doi.org/10.1016/j.chemosphere.2016.09.136
- Espitia-Perez L., da Silva J., Espitia-Perez P., Brango H., Salcedo-Arteaga S., Hoyos-Giraldo L.S., et al. Cytogenetic instability in populations with residential proximity to open-pit coal mine in Northern Colombia in relation to PM 10 and PM 2.5 levels. Ecotoxicol. Environ. Saf. 2018; 148: 453–66. https://doi.org/10.1016/j.ecoenv.2017.10.044
- Kapka L., Baumgartner A., Siwinska E., Knudsen L.E., Anderson D., Mielzynska D. Environmental lead exposure increases micronuclei in children. Mutagenesis. 2007; 22(3): 201–7. https://doi.org/10.1093/mutage/gem004
- Volkova A.T., Tselousova O.S., Potapova I.A. Cytogenetic monitoring of the risk of environmental impact on public health in the Republic of Bashkortostan. Analiz riska zdorov’yu. 2014; (3): 57-61. https://doi.org/10.21668/health.risk/2014.3.07 (in Russian)
- Ladnova G.G., Istomin A.V., Kurochitskaya M.G., Silyutina V.V. Cytogenetic indices of buccal epithelium in schoolchildren residing in territories with different levels of the air pollution. Gigiena i Sanitaria (Hygiene and Sanitation, Russian journal). 2016; 95(5): 428–31. https://doi.org/10.18821/0016-9900-2016-95-5-428-431 (in Russian)
- Byakhova M.M., Sycheva L.P., Zhurkov V.S., Gelshteyn V.S., Sukhareva I.V., Shishkina L.I., et al. Karyological and immunological parameters in children under conditions of varying ambient air pollution. Gigiena i Sanitaria (Hygiene and Sanitation, Russian journal). 2010; 89(3): 9–11. (in Russian)
- Sycheva L.P., Mozhaeva T.E., Umnova N.V., Zhuchenko N.A., Ziep B.Kh., Tuet Kh.A. Cytogenetic and other cariological parameters of exfoliative buccal cells in Vietnamese children from areas where dioxin-containing herbicides were applied. Vestnik Rossiyskoy akademii meditsinskikh nauk. 2008; (1): 19–23. (in Russian)
- Dzhambetova P.M., Molochaeva L.G., Makhtieva A.B., Sycheva L.P. Assessment of influence of petroleum pollutions of soils on the cytogenetic status and indexes of apoptosis in the cells of buccal epithelium of children. Ekologicheskaya genetika. 2009; 7(4): 34–40. https://doi.org/10.17816/ecogen7434-40 (in Russian)
- Linhares D.P.S., Garcia P.V., Silva C., Barroso J., Kazachkova N., Pereira R., et al. DNA damage in oral epithelial cells of individuals chronically exposed to indoor radon (222 Rn) in a hydrothermal area. Environ. Geochem. Health. 2018; 40(5): 1713–24. https://doi.org/10.1007/s10653-016-9893-2
- Meyer A.V., Druzhinin V.G., Larionov A.V., Tolochko T.A. Genotoxic and cytotoxic effects in buccal cells of children living in ecologically different Kuzbass areas. Tsitologiya. 2010; 52(4): 305–10. (in Russian)
- Villarini M., Levorato S., Salvatori T., Ceretti E., Bonetta S., Carducci A., et al. Buccal micronucleus cytome assay in primary school children: A descriptive analysis of the MAPEC_LIFE multicenter cohort study. Int. J. Hyg. Environ. Health. 2018; 221(6): 883–92. https://doi.org/10.1016/j.ijheh.2018.05.014
- Yurchenko V.V., Ingel F.I., Yurtseva N.A., Krivtsova E.K., Akhaltseva L.V. Effects of genome instability in limphocytes and buccal epitheliocytes of children from the city with big pulp and paper industry. Gigiena i Sanitaria (Hygiene and Sanitation, Russian journal). 2019; 98(12): 1392–401. https://doi.org/10.18821/0016-9900-2019-98-12-1392-1401 (in Russian)
- Ingel F.I., Legostaeva T.B., Antipanova N.A., Krivtsova E.K., Yurtseva N.A. System for choice of potentially carcinogenic compounds among ones, persisting in atmospheric air and having high priority for future hygienic regulation. Gigiena i Sanitaria (Hygiene and Sanitation, Russian journal). 2012; 91(6): 33–6. (in Russian)
- Migliore L., Coppede F., Fenech M., Thomas P. Association of micronucleus frequency with neurodegenerative diseases. Mutagenesis. 2011; 26(1): 85–92. https://doi.org/10.1093/mutage/geq067
- Porciello G., Scarpato R., Ferri C., Storino F., Cagetti F., Morozzi G., et al. Spontaneous chromosome damage (micronuclei) in systemic sclerosis and Raynaud’s phenomenon. J. Rheumatol. 2003; 30(6): 1244–7.
- Salimi M., Broumand B., Mozdarani H. Association of elevated frequency of micronuclei in peripheral blood lymphocytes of type 2 diabetes patients with nephropathy complications. Mutagenesis. 2016; 31(6): 627–33. https://doi.org/10.1093/mutage/gew029
- Countryman I.P., Heddle A.J. The production of micronuclei from chromosome aberrations in irradiated cultures of human lymphocytes. Mutat. Res. 1976; 41(2-3): 321–31. https://doi.org/10.1016/0027-5107(76)90105-6
- Holland N., Dave V., Venkat S., Wong H., Donde A., Balmes J.R., et al. Ozone inhalation leads to a dose-dependent increase of cytogenetic damage in human lymphocytes. Environ. Mol. Mutagen. 2015; 56(4): 378–87. https://doi.org/10.1002/em.21921
- Yurchenko V.V. Cytogenetic disorders in the human cheek epithelium upon exposure to genotoxicants. Toksikologicheskiy vestnik. 2005; 6: 14–21. (in Russian)
- Sycheva L.P., Sheremet’eva S.M. Micronucleus test on urothelial epithelial cells. In: Multiorgan Micronuclear test in Environmental Hygienic Research [Poliorgannyy mikroyadernyy test v ekologo-gigienicheskikh issledovaniyakh]. Moscow; 2007: 277–86. (in Russian)
- Gandhi G., Kaur B. Elevated friquency of micronuclei in uterine smears of cervix cancer patients. Caryologia. 2003; 56(2): 217–22. https://doi.org/10.1080/00087114.2003.10589328
- Kovalenko M.A., Sycheva L.P. Micronucleus test on nasal epithelial cells. In: Multiorgan Micronuclear test in Environmental Hygienic Research [Poliorgannyy mikroyadernyy test v ekologo-gigienicheskikh issledovaniyakh]. Moscow; 2007: 268–76. (in Russian)
- Ye C.Y., Sharpe Z., Alemara S., Mackenzie S., Liu G., Abdallah B., et al. Micronuclei and genome chaos: changing the system inheritance. Genes. 2019; 10(5): 366–87. https://doi.org/10.3390/genes10050366
- Ingel F.I. Micronucleus method on human peripheral blood lymphocytes. In: Multiorgan Micronuclear test in Environmental Hygienic Research [Poliorgannyy mikroyadernyy test v ekologo-gigienicheskikh issledovaniyakh]. Moscow; 2007: 168–219. (in Russian)
- Fenech M., Morley A. Solutions to the kinetic problem in the micronucleus assay. Cytobios. 1985; 43(172–3): 233–46.
- Fenech M. A mathematical model of the in vitro micronucleus assay predicts false negative results if micronuclei are not specifically scored in binucleated cells or in cells that have completed one nuclear division. Mutagenesis. 2000; 15(4): 329–36. https://doi.org/10.1093/mutage/15.4.329
- Haaf T., Raderschall E., Reddy G., Ward D.C., Radding C.M., Golub E.I. Sequestration of mammalian Rad51-recombination protein into micronuclei. J. Cell Biol. 1999; 144(1): 11–20. https://doi.org/10.1083/jcb.144.1.11
- Shimizu N., Itoh N., Utiyama H., Wahl G.M. Selective entrapment of extrachromosomally amplified DNA by nuclear budding and micronucleation during S phase. J. Cell Biol. 1998; 140(6): 1307–20. https://doi.org/10.1083/jcb.140.6.1307
- Kirch-Volders M., Fenech M. Inclusion of micronuclei in non-divided mononuclear lymphocytes and necrosis/apoptosis may provide a more comprehensive cytokinesis block micronucleus assay for biomonitoring purposes. Mutagenesis. 2001; 16(1): 51–8. https://doi.org/10.1093/mutage/16.1.51
- Fenech M. Cytokinesis-block micronucleus cytome assay. Nat. Protoc. 2007; 2(5): 1084–104. https://doi.org/10.1038/nprot.2007.77
- Stavropoulou V., Xie J., Henriksson M., Tomkinson B., Imreh S., Masucci M.G. Mitotic infidelity and centrosome duplication errors in cells overexpressing tripeptidyl-peptidase. Cancer Res. 2005; 65(4): 1361–8. https://doi.org/10.1158/0008-5472.CAN-04-2085
- Eastmond D.A., Tucker J.D. Identification of aneuploidy-inducing agents using cytokinesis-blocked human lymphocytes and an antikinetochore antibody. Environ. Mol. Mutagen. 1989; 13(1): 34–43. https://doi.org/10.1002/em.2850130104
- Fenech M. Cytokinesis-block micronucleus assay evolves into a “cytome” assay of chromosomal instability, mitotic dysfunction and cell death. Mutat. Res. 2006; 600(1–2): 58–66. https://doi.org/10.1016/j.mrfmmm.2006.05.028
- Fenech M., Bonassi S., Turner J., Lando C., Ceppi M., Chang W.P., et al. Human MicroNucleus project Intra- and inter-laboratory variation in the scoring of micronuclei and nucleoplasmic bridges in binucleated human lymphocytes. Results of an international slide-scoring exercise by the HUMN project. Mutat. Res. 2003; 534(1-2): 45–64. https://doi.org/10.1016/s1383-5718(02)00248-6
- Fenech M., Chang W.P., Kirsch-Volders M., Holland N., Bonassi S., Zeiger E., et al. HUMN project: detailed description of of the scoring criteria for the cytokinesis-block micronucleus assay using isolated human lymphocyte cultures. Mutat. Res. 2003; 534(1-2): 65–75. https://doi.org/10.1016/s1383-5718(02)00249-8
- Koss L.G. Diagnostic Cytology and its Histopathologic Bases. Volume 1, 2. Philadelphia-Toronto; 1979.
- El-Zein R.A., Abdel-Rahman S., Santee K.J., Yu R., Shete S. Identification of small and non-small cell lung cancer markers in peripheral blood using cytokinesis-blocked micronucleus and spectral karyotyping assays. Cytogenet. Genome Res. 2017; 152(3): 122–31. https://doi.org/10.1159/000479809
- Ingel’ F.I., Krivtsova E.K., Yurtseva N.A., Antipanova N.A., Legostaeva T.B. Volatility and sensitivity of the genome of healthy children in Magnitogorsk. Gigiena i Sanitaria (Hygiene and Sanitation, Russian journal). 2013; 92(3): 20–7. (in Russian)
- Martelli A., Robbiano L., Cosso M., Perrone C., Tagliazucchi A., Giuliano L., et al. Comparison of micronuclei frequencies in mono-, bi- and poly-nucleated lymphocytes from subjects of a residential suburb and subjects living near a metallurgical plant. Mutat. Res. 2000; 470(2): 211–9. https://doi.org/10.1016/s1383-5718(00)00108-x
- Bonassi S., Fenech M., Lando C., Lin Y., Ceppi M., Chang W.P., et al. HUman MicroNucleus project: international database comparison for results with the cytokinesis-block micronucleus assay in human lymphocytes: 1. Effect of laboratory protocol, scoring criteria, and host factors on the frequency of micronuclei. Environ. Mol. Mutagen. 2001; 37(1): 31–45.
- Bolognesi C., Knasmueller S., Nersesyan A., Roggieri P., Ceppi M., Bruzzone M., et al. Inter-laboratory consistency and variability in the buccal micronucleus cytome assay depends on biomarker scored and laboratory experience: Results from the HUMNxl international inter-laboratory scoring exercise. Mutagenesis. 2017; 32(2): 257–66. https://doi.org/10.1093/mutage/gew047
- Bolognesi C., Knasmueller S., Nersesyan A., Thomas P., Fenech M. The HUMNx1 scoring criteria for different cell types and nuclear anomalies in the buccal micronucleus cytome assay – An update and expanded photogallery. Mutat. Res. 2013; 753(2): 100–13. https://doi.org/10.1016/j.mrrev.2013.07.002
- Fenech M., Holland N., Zeiger E., Chang W.P., Burgaz S., Thomas Ph., et al. The HUMN and HUMNxL international collaboration projects on human micronucleus assays in lymphocytes and buccal cells – past, present and future. Mutagenesis. 2011; 26(1): 239–45. https://doi.org/10.1093/mutage/geq051
Supplementary files
