Abstract
The role of genetic susceptibility to the development of lymphoma is confirmed by the accumulating data on common genetic variants of the genes involved in lymphomogenesis. The varieties of disease variants, as well as the small effect of each of the polymorphisms, require the analysis of these markers in individual histological lymphoma subtypes in haplotype groups. This study was carried out to analyze the frequencies of rs1042522, rs1625895, and rs17878362, their triple haplotypes, and linkage disequilibrium in patients with diffuse small B-cell lymphoma and a control group. The absence of pronounced linkage disequilibrium between the rs17878362, rs1042522, and rs1625895 markers of the TP53 gene in the population control sample was revealed. At the same time, data on significant linkage disequilibrium between rs1625895 and rs1042522, as well as rs1625895 and rs17878362, and on moderate linkage disequilibrium between rs17878362 and rs1042522 in the group of patients with lymphoma were obtained. An association of the haplotype wArgG in the homozygous state with a predisposition to the development of diffuse small B-cell lymphoma was found.
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REFERENCES
Blombery, P.A., Wall, M., and Seymour, J.F., The molecular pathogenesis of B-cell non-Hodgkin lymphoma, Eur. J. Haematol., 2015, vol. 95, no. 4, pp. 280–293.
Van Valkenburg, M.E., Pruitt, G.I., Brill, I.K., et al., Family history of hematologic malignancies and risk of multiple myeloma: differences by race and clinical features, Cancer Causes Control, 2016, no. 27, pp. 81–91.
Voropaeva, E.N., Pospelova, T.I., Voevoda, M.I., et al., Association of DNA repair gene XRCC1 polymorphism Arg399Gln with high-grade non-Hodgkin’s lymphoma risk, Gematol. Transfuziol., 2013, vol. 58, no. 1, pp. 10–14.
Berezina, O.V., Vainer, A.S., Voropaeva, E.N., et al., Influence of single-nucleotide replacements in genes of folate cycle on risk of aggressive non-Hodgkin’s lymphoma development, Sib. Med. Obozr., 2011, vol. 3, no. 69, pp. 22–26.
Fan, C., Wei, J., Yuan, C., et al., The functional TP53 rs1042522 and MDM4 rs4245739 genetic variants contribute to non-Hodgkin lymphoma risk, PLoS One, 2014, vol. 9, no. 9. e107047
Vymetalkova, V., Soucek, P., Kunicka, T., et al., Genotype and haplotype analyses of TP53 gene in breast cancer patients: association with risk and clinical outcomes, PLoS One, 2015, vol. 10, no. 7. e0134463
Trifonova, E.A., Spiridonova, M.G., Gabidulina, T.V., et al., Analysis of the MTHFR gene linkage disequilibrium structure and association of polymorphic gene variants with coronary atherosclerosis, Russ. J. Genet., 2012, vol. 48, no. 10, pp. 1035–1047. https://doi.org/10.1134/S1022795412100122
Voropaeva, E.N., Voevoda, M.I., Pospelova, T.I., et al., Intronic polymorphisms of antioncogene TP53 in patients with indolent variants of non-Hodgkin lymphomas, Adv. Gerontol., 2014, vol. 4, no. 1, pp. 42–45. https://doi.org/10.1134/S2079057014010135
Perez-Losada, J., Castellanos-Martin, A., and Mao, J.H., Cancer evolution and individual susceptibility, Integr. Biol. (Cambridge), 2011, vol. 3, no. 4, pp. 316–328.
Azzam, G.A., Frank, A.K., Hollstein, M., et al., Tissue-specific apoptotic effects of the p53 codon 72 polymorphism in a mouse model, Cell Cycle, 2011, vol. 10, no. 9, pp. 1352–1355.
Wu, X., Zhao, H., Amos, C.I., et al., P53 genotypes and haplotypes associated with lung cancer susceptibility and ethnicity, J. Nat. Cancer Inst., 2002, vol. 94, no. 9, pp. 681–690.
Škereňová, M., Halašová, E., Matáková, T., et al., Low variability and stable frequency of common haplotypes of the TP53 gene region in colorectal cancer patients in a Slovak population, Anticancer Res., 2017, vol. 37, no. 4, pp. 1901–1907.
Marcel, V., Tran, P.L., Sagne, C., et al., G-quadruplex structures in TP53 intron 3: role in alternative splicing and in production of p53 mRNA isoforms, Carcinogenesis, 2011, vol. 32, no. 3, pp. 271–278.
Weng, Y., Lu, L., Yuan, G., et al., P53 codon 72 polymorphism and hematological cancer risk: an update meta-analysis, PLoS One, 2011, vol. 7, no. 9. e45820
Pospelova, T.I., Voropaeva, E.N., Voevoda, M.I., et al., p53 gene polymorphism as a potential marker of predisposition to the development of non-Hodgkin malignant lymphomas, Gematol. Transfuziol., 2010, vol. 55, no. 1, pp. 11–17.
Cherdyntseva, N.V., Denisov, E.V., Litviakov, N.V., et al., Crosstalk between the FGFR2 and TP53 genes in breast cancer: data from an association study and epistatic interaction analysis, DNA Cell Biol., 2012, vol. 31, no. 3, pp. 306–316.
Smetannikova, N.A., Maksimov, V.N., Ustinov, S.N., et al., Genotypes and haplotypes for the p53 oncosuppressor gene: association with life span in Russians from Novosibirsk oblast, Sib. Onkol. Zh., 2006, vol. 2, no. 18, pp. 37–41.
Conrad D.F., Jakobsson M., Coop G., et al., A worldwide survey of haplotype variation and linkage disequilibrium in the human genome, Nat. Genet., 2006, no. 38, pp. 1251–1260.
Khrunin A.V., Tarskaia L.A., Spitsyn V.A., et al., P53 polymorphisms in Russia and Belarus: correlation of the 2-1-1 haplotype frequency with longitude, Mol. Genet. Genomics, 2005, vol. 272, no. 6, pp. 666–672.
Hsieh L.L., Huang T.H., Chen I.H., et al., P53 polymorphisms associated with mutations in and loss of heterozygosity of the p53 gene in male oral squamous cell carcinomas in Taiwan. Br. J. Cancer., 2005, vol. 92, no. 1, pp. 30–35.
Mitra, S., Misra, C., Singh, R.K., et al., Association of specific genotype and haplotype of p53 gene with cervical cancer in India, J. Clin. Pathol., 2005, vol. 58, no. 1, pp. 26–31.
Mitra, S., Sikdar, N., Misra, C., et al., Risk assessment of p53 genotypes and haplotypes in tobacco-associated leukoplakia and oral cancer patients from eastern India, Int. J. Cancer, 2005, vol. 117, no. 5, pp. 786–793.
Voropaeva, E.N., Voevoda, M.I., Pospelova, T.I., and Maksimov, V.N., Linkage disequilibrium and haplotypes of the rs1042522, rs1625895, and rs1787862 markers of TP53 in patients with diffuse large B-cell lymphoma, Mol. Biol. (Moscow), 2014, vol. 48, no. 5, pp. 664–670. https://doi.org/10.1134/S0026893314050173
Voropaeva, E.N., Pospelova, T.I., and Voevoda, M.I., Gen TR53 pri diffuznoi V-krupnokletochnoi limfome (TP53 Gene in Patients with Diffuse Large B-Cell Lymphoma), Novosibirsk: Nauka, 2018.
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This work was carried out as part of the state-funded budget project no. 0324-2018-0002.
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Statement of compliance with standards of research involving humans as subjects. All procedures performed in the study involving people are consistent with the ethical standards of the institutional and/or national committee for research ethics and the 1964 Helsinki Declaration and its subsequent changes or comparable ethical standards.
All of the patients gave their informed consent before the study.
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Voropaeva, E.N., Cherdyntseva, N.V., Voevoda, M.I. et al. Triple Haplotypes of the TP53 Gene in Patients with Diffuse Small B-Cell Lymphoma. Russ J Genet 55, 1564–1568 (2019). https://doi.org/10.1134/S1022795419120123
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DOI: https://doi.org/10.1134/S1022795419120123