Apo-1/fas, ctla-4 and bcl-2 genes polymorphism in patients, operated on nodular thyroid pathology
DOI:
https://doi.org/10.11603/2414-4533.2017.2.7949Keywords:
nodular goiter on the background of autoimmune thyroiditis, thyroid adenoma, polymorphisms APO-1/Fas, CTLA-4 and BCL-2 genes.Abstract
The aim of the work: to analyze the frequency of polymorphic variants of genes BCL-2 (rs17759659), CTLA-4 (rs231775), APO-1/ Fas (rs2234767) in patients, operated on nodular thyroid pathology with regard to its form (NGAIT, TA- thyroid adenoma).
Materials and Methods. An analysis of the frequency of polymorphic variants of genes BCL-2 (rs17759659), CTLA-4 (rs231775), APO-1/Fas (rs2234767) in 125 patients, operated on nodular thyroid pathology with regard to its form (NGAIT, TA) was conducted. Also, we examined 25 healthy donors. The study of polymorphism of genes was carried out by the method of polymerase chain reaction in real time.
Results and Discussion. Mutation of BCL-2 gene (rs17759659) and CTLA-4 (rs231775) in the homozygous state among patients, operated on nodular thyroid pathology occurs with a frequency 3.2–4.0 % no reliable difference between patients with thyroid pathology and healthy. Mutation of the gene APO-1/Fas (rs2234767) in the homozygous state among surveyed patients was not met at all.
References
Sheremet, М.І., Sydorchuk, L.P., Shidlovskyi, V.О. & Bedeniuk, A.D. (2016). Research of prognostic markers of proliferation and apoptosis in patients with nodular goiters combined with autoimmune thyroiditis. Archives of the Balkan Medical Union, 51, (4), 488-491.
Tsyganenko, O.S. & Voroschuk, R.S. (2007). Immunomorfological reaction in the thyroid tissue in patients with autoimmune thyroiditis in combination with nodular goiter. Arta Medica. Nicholas Anestiadi, Tenth Congress of the Association of Surgeons of Moldova: Chisinau. October; 4 (25), 51-52.
Sheremet, М.І., Sydorchuk, L.P., Shidlovskyi, V.О. & Bedeniuk, A.D. (2017). New prognostistic markers of nodular forms of goiter combined with autoimmune thyroiditis. Journal of Education, Health and Sport, 7, (3), 475-482.
Sydorchuk, L.P., Sydorchuk, A.R., Sheremet, M.I. & Sydorchuk, R.I. (2017). Cytokines cascade changes in patients with rheumatoid arthritis depending on endothelial no-synthase (T-786C) genes polymorphism. Archives of the Balkan Medical Union, 52, (1), 32-38.
Sydorchuk, L.P., Iftoda, O.M., & Kushnir, O.V. (2017). Polimorfizm heniv konneksinu 26 (GJB2) ta interleykinu 4 (S-590T) u ditei – zhyteliv Bukovyny iz vtratoiu slukhu [Genes polymorphism of connexin 26 (GJB2) and interleukin 4 (C-590T) in children of Bukovyna with hearing loss]. Lik. Sprava – Treatment Case, 5-6 (1139) [in Ukrainian].
Sydorchuk, L.P. & Amosova, K.M. (2011). Influence of pharmacogenetically determined treatment on parameters of peripheral hemodynamics in patients with arterial hypertension. The New Armenian Medical J., 5, (2), 35-43.
Lee, Y.H, Choi, S.J., Ji J.D., & Song, G.G. (2012). CTLA-4 and TNF-α promoter-308 A/G polymorphisms and ANCA-associated vasculitis susceptibility: a meta-analysis. Mol. Biol. Rep. 39 (1), 319-326.
Leithäuser, F, Dhein, J., Mechtersheimer, G. (1993). Constitutive and induced expression of APO-1, a new member of the nerve growth factor/tumor necrosis factor receptor superfamily, in normal and neoplastic cells. Lab. Invest., 69, 415-429.
Man-Man Lu, Qian-Ling, Ye, & Chen-Chen, Feng (2012). Association of FAS gene polymorphisms with systemic lupus erythematosus: A case-control study and meta-analysis. Experimental and Therapeutic Medicine, 4, 497-502.
Byktagyrova, E.M., Sattarova, L.Y., Vagapova, H.R., & Kravtsova O.A. (2011). Assotsyatsyya polimorfizmov genov IL-1B, IL-4 Y IL-6 s formirovaniem geneticheskoy predraspolozhennosti k autoimmunnomu tyreoiditu. [Association of polymorfyzmov genes IL-1Β, IL-4 and IL-6 with Formation genetic predisposition for autoymmunnomu thyroiditis]. Meditsinskaya immunologiya – Medical Immunology, 13 (6), 603-608 [in Russian].
Dong, Y.H., & Fu, D.G. (2014). Autoimmune thyroid disease: mechanism, genetics and current knowledge. Eur. Rev. Med. Pharmacol. Sci., 18 (23), 3611-3618.
Tomer, Y., & Davies, T.F. (2003). Searching for the autoimmune thyroid disease susceptibility genes: from gene mapping to gene function. Endocr. Rev., 24 (5), 694-717. doi: 10.1210/er.2002-0030.
Nikitin, Yu.P., Rymar, O.D., Maksimov, V.N. (2008). Polimorfizm A49G gena tsytotoksicheskogo T-limfotsytsvyazannogo immunoglobulina 4 (CTLA4), svyaz z autoimmunnymi zabolevaniyami shchitovidnoy zhelezy v populyatsii Novosibirska [Association of the T-cell regulatory gene CTLA-4 with susceptibility to autoimmune thyroid disease in population of Novosibirsk]. Klinicheskaya i eksperimentalnaya tireoidologiya – Clinical and Experimental Thyroidology, 4 (4), 41-45 [in Russian] doi: 10.14341/ket20084441-45.
Zhang, M., Ni, J., Xu, W.D. (2014). Association of CTLA-4 variants with susceptibility to inflammatory bowel disease: a meta-analysis. Hum. Immunol., 75 (3), 227-233.
Qiu, H., Tang, W., Yin, P., Cheng, F., & Wang, L. (2014). Cytotoxic T-lymphocyte associated antigen 4 polymorphism and Hashimoto's thyroiditis susceptibility: a meta-analysis. Endocrine, 45 (2), 198-205.
Biktagirova, E.M., Kravtsova, O.A., Sattarova, L.I., & Vagapova, G.R. (2010). Vliyaniye polimorfizmov genov CTLA-4 i PTPN-22 na risk razvitiya autoimmunnogo tireoidita sredi naseleniya respubliki Tatarstan [Influence of polymorphisms of CTLA-4 and PTPN-22 genes on developmental risk autoimmune thyroiditis among the population of the Republic of Tatarstan]. Meditsinskaya immunologiya – Medical Immunology, 12 (1-2), 103-114 [in Russian].
Pastuszak-Lewandoska, D., Sewerynek, E., Domańska, D. (2012). CTLA-4 gene poly-morphisms and their influence on predisposition to autoimmune thyroid diseases (Graves' disease and Hashimoto's thyroiditis). Arch. Med. Sci., 4, 8 (3), 415-421.
Brix, T.H., & Hegedus, L. Twin studies as a model for exploring the aetiology of autoimmune thyroid disease. Clin. Endocrinol. (Oxf)., 76 (4), 457-464. doi: 10.1111/j.1365-2265.2011.04318.
Kochetova, O.V., Gaynullina, M.K., & Viktorova, T.V. (2014). DIO2, TPO, CYP1A1 AND CYP1A2 gene polymorphism in women with thyroid disease. Gig. Sanit., (3), 52-56.
Gözü, H.I., Özçelik, S. Aloğlu, M., Şahin, A., Temiz, S., Dayan, A. … Cengiz, H. (2016). Is the TSHR D727E polymorphism a genetic predisposition for multinodular goiter in the Turkish population? Genet. Mol. Res., 15 (3), 385-390.
Population Diversity (Alleles in RefSNP orientation). / dbSNP Short Genetic Variation // NCBI. – 2017. – URL: http://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi? searchType=adhoc_search&type =rs&rs=rs17759659
b. Population Diversity (Alleles in RefSNP orientation). / dbSNP Short Genetic Variation // NCBI. – 2017. – URL: http://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi? searchType=adhoc_search&type =rs&rs=231775
c. Population Diversity (Alleles in RefSNP orientation). / dbSNP Short Genetic Variation // NCBI. – 2017. – URL: http://www.ncbi.nlm.nih.gov/SNP/snp_ref.cgi? searchType=adhoc_search&type =rs&rs=2234767
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