Several single nucleotide polymorphisms in survivin gene promoters, notably -31G/C, have been shown to modulate the expression and activity of the survivin protein. Consequently, the -31G/C polymorphism has been identified as a risk factor for the development of several types of tumors. The aim of this study was to investigate a possible association between the -31G/C polymorphism and the risk for keratocystic odontogenic tumor (KCOT) development. DNA from 52 biopsy specimens of KCOTs and from 82 buccal swabs of healthy individuals was subjected to PCR restriction fragment length polymorphism analysis to identify individual genotypes. The distribution of genotypes in KCOT and control groups, respectively, was: GG: 30 (57.7%) vs. 26 (31.7%); CG: 17 (32.7%) vs. 45 (54.9%); and CC: 5 (9.6%) vs. 11 (13.4%), respectively. These differences were statistically significant. The G allele was more common in the KCOT group than in the control group: 76 (74%) vs. 96 (59%), respectively. Logistic r...egression analysis showed that GC heterozygotes had a considerably decreased susceptibility for KCOTs compared with GG homozygotes. The same was true for GC+CC vs. GG. The GG genotype of the -31G/C polymorphism might be a risk factor for KCOT development.
TY - JOUR
AU - Andrić, Miroslav
AU - Nikolić, Nadja
AU - Bosković, Marija
AU - Miličić, Biljana
AU - Skodrić, Sanja
AU - Basta-Jovanović, Gordana
AU - Milašin, Jelena
PY - 2012
UR - https://smile.stomf.bg.ac.rs/handle/123456789/1755
AB - Several single nucleotide polymorphisms in survivin gene promoters, notably -31G/C, have been shown to modulate the expression and activity of the survivin protein. Consequently, the -31G/C polymorphism has been identified as a risk factor for the development of several types of tumors. The aim of this study was to investigate a possible association between the -31G/C polymorphism and the risk for keratocystic odontogenic tumor (KCOT) development. DNA from 52 biopsy specimens of KCOTs and from 82 buccal swabs of healthy individuals was subjected to PCR restriction fragment length polymorphism analysis to identify individual genotypes. The distribution of genotypes in KCOT and control groups, respectively, was: GG: 30 (57.7%) vs. 26 (31.7%); CG: 17 (32.7%) vs. 45 (54.9%); and CC: 5 (9.6%) vs. 11 (13.4%), respectively. These differences were statistically significant. The G allele was more common in the KCOT group than in the control group: 76 (74%) vs. 96 (59%), respectively. Logistic regression analysis showed that GC heterozygotes had a considerably decreased susceptibility for KCOTs compared with GG homozygotes. The same was true for GC+CC vs. GG. The GG genotype of the -31G/C polymorphism might be a risk factor for KCOT development.
PB - Wiley-Blackwell, Hoboken
T2 - European Journal of Oral Sciences
T1 - Survivin gene promoter polymorphism-31G/C as a risk factor for keratocystic odontogenic tumor development
VL - 120
IS - 1
SP - 9
EP - 13
DO - 10.1111/j.1600-0722.2011.00919.x
ER -
@article{
author = "Andrić, Miroslav and Nikolić, Nadja and Bosković, Marija and Miličić, Biljana and Skodrić, Sanja and Basta-Jovanović, Gordana and Milašin, Jelena",
year = "2012",
abstract = "Several single nucleotide polymorphisms in survivin gene promoters, notably -31G/C, have been shown to modulate the expression and activity of the survivin protein. Consequently, the -31G/C polymorphism has been identified as a risk factor for the development of several types of tumors. The aim of this study was to investigate a possible association between the -31G/C polymorphism and the risk for keratocystic odontogenic tumor (KCOT) development. DNA from 52 biopsy specimens of KCOTs and from 82 buccal swabs of healthy individuals was subjected to PCR restriction fragment length polymorphism analysis to identify individual genotypes. The distribution of genotypes in KCOT and control groups, respectively, was: GG: 30 (57.7%) vs. 26 (31.7%); CG: 17 (32.7%) vs. 45 (54.9%); and CC: 5 (9.6%) vs. 11 (13.4%), respectively. These differences were statistically significant. The G allele was more common in the KCOT group than in the control group: 76 (74%) vs. 96 (59%), respectively. Logistic regression analysis showed that GC heterozygotes had a considerably decreased susceptibility for KCOTs compared with GG homozygotes. The same was true for GC+CC vs. GG. The GG genotype of the -31G/C polymorphism might be a risk factor for KCOT development.",
publisher = "Wiley-Blackwell, Hoboken",
journal = "European Journal of Oral Sciences",
title = "Survivin gene promoter polymorphism-31G/C as a risk factor for keratocystic odontogenic tumor development",
volume = "120",
number = "1",
pages = "9-13",
doi = "10.1111/j.1600-0722.2011.00919.x"
}
Andrić, M., Nikolić, N., Bosković, M., Miličić, B., Skodrić, S., Basta-Jovanović, G.,& Milašin, J.. (2012). Survivin gene promoter polymorphism-31G/C as a risk factor for keratocystic odontogenic tumor development. in European Journal of Oral Sciences
Wiley-Blackwell, Hoboken., 120(1), 9-13.
https://doi.org/10.1111/j.1600-0722.2011.00919.x
Andrić M, Nikolić N, Bosković M, Miličić B, Skodrić S, Basta-Jovanović G, Milašin J. Survivin gene promoter polymorphism-31G/C as a risk factor for keratocystic odontogenic tumor development. in European Journal of Oral Sciences. 2012;120(1):9-13.
doi:10.1111/j.1600-0722.2011.00919.x .
Andrić, Miroslav, Nikolić, Nadja, Bosković, Marija, Miličić, Biljana, Skodrić, Sanja, Basta-Jovanović, Gordana, Milašin, Jelena, "Survivin gene promoter polymorphism-31G/C as a risk factor for keratocystic odontogenic tumor development" in European Journal of Oral Sciences, 120, no. 1 (2012):9-13,
https://doi.org/10.1111/j.1600-0722.2011.00919.x . .
