Association study of 6 candidate single-nucleotide polymorphisms (rs7921, rs7956547, rs3761243, rs11737764, rs6599400, rs1690916) was carried out in a group of patients with bone tumors of different histological structure (n=68) and control group of normal subjects (n=96). Significant associations of rs6599400 and rs1690916 polymorphisms with disease risk were detected (odds ratio 2.15 [1.06-4.24] and 0.39 [0.19-0.78], respectively). These polymorphisms were located in untranslated genome regions: polymorphism rs6599400 in the 5’ region of fibroblast growth factor-3 receptor gene (FGFR3), rs1690916 in the 3’ region of mouse MDM2 p53-binding protein homolog (MDM2). These data indicated a possible role of hereditary genetic factors in the formation of predisposition to bone sarcomas and confirmed previous findings according to which these genes should be regarded among the most probable factors involved in tumor development, including tumors of the bone and cartilage tissues.
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Translated from Byulleten’ Eksperimental’noi Biologii i Meditsiny, Vol. 153, No. 6, pp. 850-855, June, 2012
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Naumov, V.A., Generozov, E.V., Solovyov, Y.N. et al. Association of FGFR3 and MDM2 Gene Nucleotide Polymorphisms with Bone Tumors. Bull Exp Biol Med 153, 870–874 (2012). https://doi.org/10.1007/s10517-012-1847-9
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DOI: https://doi.org/10.1007/s10517-012-1847-9