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Genotype TNF-α(-308) and Silicosis on Factory Workers in Vietnam in 2020

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The studFigy aims to determine the TNF-α single-nucleotide polymorphism TNF-α (-308) and assess the association of TNF-a(-308) SNP with the risk of silicosis among workers directly exposed to silica dust in Vietnam. A study was undertaken among 78 cases with silicosis and 103 controls without silicosis in Vietnam. Blood samples were collected for genomic DNA extraction from each subject. The phenotyping of TNF-α(-308) was performed using polymerase chain reaction‐based restriction fragment length polymorphism (PCR‐RFLP) and dye termination sequencing. Results: The average exposure time of the case group was slightly higher than that of the control group (12.46 ± 6.732 years vs. 12.09 ± 7.854 years). The majority of genotypes in both silicosis and non-silicosis was GG. When analyzing the concentration of TNF-α in the study participants' blood, it is shown that the average concentration of TNFα in the case group was higher than that in the control group. The genotype AG in the case group was 1.368 times higher than that in the control group. The percentage of all A alleles in the case group with silicosis was 1.342 times higher than the control group without the disease, similar to previous studies. Conclusion: The majority of genotypes in both groups was GG. The average concentration of TNF-α in blood, genotype AG, and the percentage of all A alleles in the case group was higher than that in the control group.
Słowa kluczowe
EN
PL
Rocznik
Tom
Strony
459--466
Opis fizyczny
Bibliogr. 22 poz., tab., wykr.
Twórcy
autor
  • Vietnam National Cancer Institute, Vietnam National Cancer Hospital, Hanoi, Vietnam
  • Hanoi University of Public Health, Hanoi, Vietnam
  • Health Environment Management Agency, Ministry of Health, Hanoi, Vietnam
autor
  • Hanoi Medical University, Hanoi, Vietnam
autor
  • Hanoi Medical University, Hanoi, Vietnam
  • Hanoi Medical University, Hanoi, Vietnam
  • Hanoi Medical University, Hanoi, Vietnam
  • Hanoi Medical University, Hanoi, Vietnam
autor
  • Hanoi Medical University, Hanoi, Vietnam
  • Hanoi Medical University, Hanoi, Vietnam
  • National Lung Hospital, Hanoi, Vietnam
  • National Lung Hospital, Hanoi, Vietnam
  • Health Environment Management Agency, Ministry of Health, Hanoi, Vietnam
  • Hanoi Medical University, Hanoi, Vietnam
Bibliografia
  • 1. Ministry of Health of Viet Nam. TT15/2016 TT-BYT. Regulations on occupational diseases entitled to social insurance. 2016.
  • 2. Lopes-Pacheco, M, Bandeira E, Morales MM.,2016. Cell-Based Therapy for Silicosis, Stem Cells Int, 2016, 509-518, https://doi.org/10.1155/2016/5091838.
  • 3. Wang, Y.W., Lan,J.Y., Yang, L.Y., et al., 2012. TNF-alpha and IL-1RA polymorphisms and silicosis susceptibility in Chinese workers exposed to silica particles: a case-control study, Biomedical and Environmental Sciences, 2012, 25(5): 517-525. doi: 10.3967/0895-3988.2012.05.004.
  • 4. Corbett, E.L., Mozzato-Chamay, N., Butterworth, A.E., et al., 2002. Polymorphisms in the tumor necrosis factor-alpha gene promoter may predispose to severe silicosis in black South African miners, Am J Respir Crit Care Med. 2002 Mar 1;165(5): 690-3. doi: 10.1164/ajrccm.165.5.2010050.
  • 5. Li, Z., Xue, J., Yan, S., Chen, P., et al., 2013. Association between tumor necrosis factor-α 308G/A gene polymorphism and silicosis susceptibility: a meta-analysis,PLoS One, 8, 215-220, https://doi.org/10.1371/journal.pone.0076614.
  • 6. Sullivan, K.E., Wooten, C., Schmeckpeper, B.J., et al.,1997. A promoter polymorphism of tumor necrosis factor alpha associated with systemic lupus erythematosus in African-Americans, Arthritis and rheumatism, 40(12): 2207–2211. https://doi.org/10.1002/art.1780401215.
  • 7. Kurniawidjaja, L.M., et al., 2014. Silicosis and its progress influenced by genetic variation on TNFalpha locus- 308, TNF-alpha and IL-10 cytokine on cement factory workers in Indonesia, Pakistan journal of biological sciences : PJBS, 17(3): 419-423. https://doi.org/10.3923/pjbs.2014.419.423.
  • 8. Yucesoy, B., Vallyathan, V., Landsittel, D.P., et al., 2002. Cytokine polymorphisms in silicosis and other pneumoconioses, Molecular and cellular biochemistry, 234-235(1-2): 219-224.
  • 9. Becklake, M.R.,1992. The mineral dust diseases, Tubercle and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease, 73(1): 13–20. https://doi.org/10.1016/0962-8479(92)90074-T.
  • 10.Leger, J.P., 1992. Occupational diseases in South African mines--a neglected epidemic?, South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 81(4): 197–201.
  • 11.Ortiz, L.A., Lasky, J., Lungarella, G., et al., 1999. Upregulation of the p75 but not the p55 TNFalpha receptor mRNA after silica and bleomycin exposure and protection from lung injury in double receptor knockout mice, American journal of respiratory cell and molecular biology, 20(4): 825–833. https://doi.org/10.1165/ajrcmb.20.4.3193
  • 12.Ohtsuka, Y., Munakata, M., Ukita, H., et al.,1995. Increased susceptibility to silicosis and TNF-alpha production in C57BL/6J mice, American journal of respiratory and critical care medicine, 152 (6 Pt 1): 2144–2149. https://doi.org/10.1164/ajrccm.152.6.8520788.
  • 13.Davis, G.S., Leslie, K.O., Hemenway, D.R., 1998. Silicosis in mice: effects of dose, time, and genetic strain, Journal of environmental pathology, toxicology and oncology : official organ of the International Society for Environmental Toxicology and Cancer, 17(2): 81–97.
  • 14.Hassani, E., Bagheri, M., Rad, I.A., et al., 2017. Association between SNPs at IL-17A and IL-17F and susceptibility to accelerated silicosis, Toxicology and Industrial Health, 33: 673-680, https://doi.org/10.1177/0748233717695431
  • 15.Nadif, R., Mintz, M., Marzec, J., et al., 2006. IL18 and IL18R1 polymorphisms, lung CT and fibrosis: a longitudinal study in coal miners, European Respiratory Journal 2006 28: 1100-1105; DOI: 10.1183/09031936.00031506
  • 16.Rad, I.A., Mohebbi, I., Bagheri, M., et al., 2012. Molecular Evaluation of the IFN γ +874, TNF α - 308, and IL-1Ra VNTR Sequences in Silicosis, Maedica,7(1),20-24.
  • 17.Miao, R-M., Zhang, X-T., Yan, Y-L., et al., 2011. Change of serum TGF-beta1 and TNF-alpha in silicosis patients, Chinese journal of industrial hygiene and occupational diseases, (12): 606-607.
  • 18.Slavov, E., Miteva, L., Prakova, G., et al., 2010. Correlation between TNF-alpha and IL-12p40-containing cytokines in silicosis, Toxicology and industrial health, 26(8): 479–486. https://doi.org/10.1177/0748233710373082
  • 19.Economou, J.S., Rhoades, K., Essner, R., et al.,1989. Genetic analysis of the human tumor necrosis factor alpha/cachectin promoter region in a macrophage cell line, The Journal of experimental medicine, 170(1): 321–326. https://doi.org/10.1084/jem.170.1.321
  • 20.Yucesoy, B., Vallyathan, V., Landsittel, D.P., et al., 2011. Association of tumor necrosis factor-alpha and interleukin-1 gene polymorphisms with silicosis, Toxicology and applied pharmacology, 172(1): 75–82. https://doi.org/10.1006/taap.2001.9124
  • 21.Yang, L.T., Liu, X., Wu, G.H., et al.,2018. Association between tumor necrosis factor-α -308 Gauss/A polymorphism and risk of silicosis and coal workers pneumoconiosis in Chinese population, Inhal Toxicol, 30, 213-217.
  • 22.Torres Puig-Gros, J., Alzuria Alos, R.M., et al., 2018. Concordance between the antecedents of influenza vaccination referred by pregnant women and those recorded in the medical record, Revista espanola de salud publica, 92, e201803005.
Uwagi
Opracowanie rekordu ze środków MNiSW, umowa Nr 461252 w ramach programu "Społeczna odpowiedzialność nauki" - moduł: Popularyzacja nauki i promocja sportu (2021).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-d834dee8-de3e-44df-b525-26511bb66756
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