Kostić, Marija

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  • Kostić, Marija (2)
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Author's Bibliography

Association of TNF-R2 (676T>G) single nucleotide polymorphism with head and neck cancer risk in the Serbian population

Kostić, Marija; Nikolić, Nadja; Ilić, Branislav; Jelovac, Drago; Trakilović, Slobodanka; Božović, Maja; Milašin, Jelena

(Srpsko biološko društvo, Beograd, i dr., 2013)

TY  - JOUR
AU  - Kostić, Marija
AU  - Nikolić, Nadja
AU  - Ilić, Branislav
AU  - Jelovac, Drago
AU  - Trakilović, Slobodanka
AU  - Božović, Maja
AU  - Milašin, Jelena
PY  - 2013
UR  - https://smile.stomf.bg.ac.rs/handle/123456789/1793
AB  - Tumor necrosis factor (TNF) which exerts its effects through two different receptors known as TNF-R1 and TNF-R2, is a major proinflammatory cytokine involved in the pathogenesis of different types of tumors. We have investigated whether polymorphisms in TNF-alpha (-308G>A), TNF receptor 1 (36A>G) and TNF receptor 2 (676T>G) genes modulate the susceptibility for oral squamous cell carcinomas (OSCCs) and basal cell carcinomas (BCCs) of the skin, two frequent types of head and neck cancers. Genotyping was done on 50 OSCC patients, 50 BCC patients and 60 healthy individuals, using PCR/RFLP. A significant difference in genotype and allele frequencies was found between patients and controls for the TNF-R2 polymorphism, in both OSCC and BCC. There was no statistically significant difference between patients and controls for TNF-alpha and TNF-R1 polymorphisms. Carriers of G allele had an approximately 2.5- and 5-fold higher risk for OSCC and BCC, respectively, in the Serbian population.
PB  - Srpsko biološko društvo, Beograd, i dr.
T2  - Archives of Biological Sciences
T1  - Association of TNF-R2 (676T>G) single nucleotide polymorphism with head and neck cancer risk in the Serbian population
VL  - 65
IS  - 1
SP  - 387
EP  - 393
DO  - 10.2298/ABS1301387K
ER  - 
@article{
author = "Kostić, Marija and Nikolić, Nadja and Ilić, Branislav and Jelovac, Drago and Trakilović, Slobodanka and Božović, Maja and Milašin, Jelena",
year = "2013",
abstract = "Tumor necrosis factor (TNF) which exerts its effects through two different receptors known as TNF-R1 and TNF-R2, is a major proinflammatory cytokine involved in the pathogenesis of different types of tumors. We have investigated whether polymorphisms in TNF-alpha (-308G>A), TNF receptor 1 (36A>G) and TNF receptor 2 (676T>G) genes modulate the susceptibility for oral squamous cell carcinomas (OSCCs) and basal cell carcinomas (BCCs) of the skin, two frequent types of head and neck cancers. Genotyping was done on 50 OSCC patients, 50 BCC patients and 60 healthy individuals, using PCR/RFLP. A significant difference in genotype and allele frequencies was found between patients and controls for the TNF-R2 polymorphism, in both OSCC and BCC. There was no statistically significant difference between patients and controls for TNF-alpha and TNF-R1 polymorphisms. Carriers of G allele had an approximately 2.5- and 5-fold higher risk for OSCC and BCC, respectively, in the Serbian population.",
publisher = "Srpsko biološko društvo, Beograd, i dr.",
journal = "Archives of Biological Sciences",
title = "Association of TNF-R2 (676T>G) single nucleotide polymorphism with head and neck cancer risk in the Serbian population",
volume = "65",
number = "1",
pages = "387-393",
doi = "10.2298/ABS1301387K"
}
Kostić, M., Nikolić, N., Ilić, B., Jelovac, D., Trakilović, S., Božović, M.,& Milašin, J.. (2013). Association of TNF-R2 (676T>G) single nucleotide polymorphism with head and neck cancer risk in the Serbian population. in Archives of Biological Sciences
Srpsko biološko društvo, Beograd, i dr.., 65(1), 387-393.
https://doi.org/10.2298/ABS1301387K
Kostić M, Nikolić N, Ilić B, Jelovac D, Trakilović S, Božović M, Milašin J. Association of TNF-R2 (676T>G) single nucleotide polymorphism with head and neck cancer risk in the Serbian population. in Archives of Biological Sciences. 2013;65(1):387-393.
doi:10.2298/ABS1301387K .
Kostić, Marija, Nikolić, Nadja, Ilić, Branislav, Jelovac, Drago, Trakilović, Slobodanka, Božović, Maja, Milašin, Jelena, "Association of TNF-R2 (676T>G) single nucleotide polymorphism with head and neck cancer risk in the Serbian population" in Archives of Biological Sciences, 65, no. 1 (2013):387-393,
https://doi.org/10.2298/ABS1301387K . .
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Analysis of polymorphism in the survivin gene promoter as a potential risk factor for head and neck cancers development

Kostić, Marija; Nikolić, Nadja; Ilić, Branislav; Čarkić, Jelena; Milenković, Sanja; Vukadinović, Miroslav

(Srpsko lekarsko društvo, Beograd, 2013)

TY  - JOUR
AU  - Kostić, Marija
AU  - Nikolić, Nadja
AU  - Ilić, Branislav
AU  - Čarkić, Jelena
AU  - Milenković, Sanja
AU  - Vukadinović, Miroslav
PY  - 2013
UR  - https://smile.stomf.bg.ac.rs/handle/123456789/1797
AB  - Introduction. Association studies have shown that gene polymorphisms in various classes of genes can modulate cancer risk. The -31G/C polymorphism in the promoter of survivin gene, affects the expression of the anti-apoptotic protein survivin which in turn may predispose an individual to some types of cancer. Objective. The aim of the study was to determine whether the survivin promoter -31G/C polymorphism could be a susceptibility factor for squamous cell carcinoma (SCC) of the oral cavity and basal cell carcinoma (BCC) of the skin. Methods. The DNA obtained from 88 patients with SCC, 60 patients with BCC and 111 healthy individuals was subjected to polymerase chain reaction-restriction fragment length polymorphism analysis (PCR- RFLP) in order to determine genotype and allele frequencies in patients and control groups. Logistic regression was used for cancer risk assessment. Results. The following distribution of genotypes was obtained: CC genotype 15% in the SCC group, 13% in the BCC group and 12% in controls; CG genotype 41% in SCCs, 35% in BCCs, 48% in controls; GG genotype 44% in SCCs, 52% in BCCs and 40% in controls. Allelic frequencies were as follows: G allele 0.65 in SCCs, 0.69 in BCCs and 0.64 in the control group; C allele 0.35 in SCCs, 0.31 in BCCs and 0.36 in the control group. There was no statistically significant difference in allele or genotype frequencies between the patients and controls (p>0.05). Conclusion. In Serbian population, -31G/C polymorphism in the promoter of the survivin gene cannot be considered as a risk factor for oral squamous cell carcinoma and skin basal cell carcinoma.
AB  - Uvod. Dokazano je da polimorfizmi u različitim klasama gena mogu da povećaju rizik za razvoj malignih tumora, između ostalih i skvamocelularnog karcinoma (SCC) usne duplje i bazocelularnog karcinoma (BCC) kože. Survivin je bifunkcionalni protein-inhibitor apoptoze i regulator ćelijskog ciklusa. Otkriveno je više funkcionalnih polimorfizama u ovom genu, a jedan od ključnih je polimorfizam G/C na poziciji -31, za koji je pokazano da je modulator ekspresije survivina i da doprinosi povećanju rizika od obolevanja od različitih tipova tumora. Cilj rada. Cilj rada je bio da se analizira učestalost genotipova i alela za -31G/C polimorfizam gena za survivin kod osoba obolelih od SCC i BCC i kod zdravih ispitanika. Logističkom regresionom analizom ispitana je povezanost ovog polimorfizma i rizika za nastanak SCC i BCC. Metode rada. Učestalosti alela i genotipova kod 88 osoba obolelih od SCC, 60 osoba obolelih od BCC i 111 zdravih ispitanika određene su lančanom reakcijom polimeraze i restrikcionom analizom. Logističkom regresijom procenjena je sklonost ka razvoju SCC i BCC. Rezultati. Genotip CC je utvrđen kod 15% ispitanika sa SCC, 13% sa BCC i 12% zdavih osoba. Genotip CG je zabeležen kod 41% ispitanika sa SCC, 35% sa BCC i 48% zdravih osoba. Genotip GG je otkriven kod 44% osoba sa SCC, 52% sa BCC i 40% zdravih ispitanika. Učestalost G-alela bila je sledeća: 0,65 kod ispitanika sa SCC, 0,69 kod ispitanika sa BCC i 0,64 u grupi zdravih osoba. Učestalost C-alela bila je: 0,35 kod ispitanika sa SCC, 0,31 kod ispitanika sa BCC i 0,36 u grupi zdravih osoba. Nije bilo statistički značajne razlike u raspodeli genotipova i alela između bolesnika s karcinomima i zdravih ispitanika (p>0,05). Zaključak. Polimorfizam -31G/C u promotoru gena za survivin ne može se smatrati faktorom rizika za razvoj ova dva tipa tumora.
PB  - Srpsko lekarsko društvo, Beograd
T2  - Srpski arhiv za celokupno lekarstvo
T1  - Analysis of polymorphism in the survivin gene promoter as a potential risk factor for head and neck cancers development
T1  - Analiza polimorfizma u promotoru gena za survivin kao mogućeg faktora rizika za nastanak tumora glave i vrata
VL  - 141
IS  - 5-6
SP  - 304
EP  - 307
DO  - 10.2298/SARH1306304K
ER  - 
@article{
author = "Kostić, Marija and Nikolić, Nadja and Ilić, Branislav and Čarkić, Jelena and Milenković, Sanja and Vukadinović, Miroslav",
year = "2013",
abstract = "Introduction. Association studies have shown that gene polymorphisms in various classes of genes can modulate cancer risk. The -31G/C polymorphism in the promoter of survivin gene, affects the expression of the anti-apoptotic protein survivin which in turn may predispose an individual to some types of cancer. Objective. The aim of the study was to determine whether the survivin promoter -31G/C polymorphism could be a susceptibility factor for squamous cell carcinoma (SCC) of the oral cavity and basal cell carcinoma (BCC) of the skin. Methods. The DNA obtained from 88 patients with SCC, 60 patients with BCC and 111 healthy individuals was subjected to polymerase chain reaction-restriction fragment length polymorphism analysis (PCR- RFLP) in order to determine genotype and allele frequencies in patients and control groups. Logistic regression was used for cancer risk assessment. Results. The following distribution of genotypes was obtained: CC genotype 15% in the SCC group, 13% in the BCC group and 12% in controls; CG genotype 41% in SCCs, 35% in BCCs, 48% in controls; GG genotype 44% in SCCs, 52% in BCCs and 40% in controls. Allelic frequencies were as follows: G allele 0.65 in SCCs, 0.69 in BCCs and 0.64 in the control group; C allele 0.35 in SCCs, 0.31 in BCCs and 0.36 in the control group. There was no statistically significant difference in allele or genotype frequencies between the patients and controls (p>0.05). Conclusion. In Serbian population, -31G/C polymorphism in the promoter of the survivin gene cannot be considered as a risk factor for oral squamous cell carcinoma and skin basal cell carcinoma., Uvod. Dokazano je da polimorfizmi u različitim klasama gena mogu da povećaju rizik za razvoj malignih tumora, između ostalih i skvamocelularnog karcinoma (SCC) usne duplje i bazocelularnog karcinoma (BCC) kože. Survivin je bifunkcionalni protein-inhibitor apoptoze i regulator ćelijskog ciklusa. Otkriveno je više funkcionalnih polimorfizama u ovom genu, a jedan od ključnih je polimorfizam G/C na poziciji -31, za koji je pokazano da je modulator ekspresije survivina i da doprinosi povećanju rizika od obolevanja od različitih tipova tumora. Cilj rada. Cilj rada je bio da se analizira učestalost genotipova i alela za -31G/C polimorfizam gena za survivin kod osoba obolelih od SCC i BCC i kod zdravih ispitanika. Logističkom regresionom analizom ispitana je povezanost ovog polimorfizma i rizika za nastanak SCC i BCC. Metode rada. Učestalosti alela i genotipova kod 88 osoba obolelih od SCC, 60 osoba obolelih od BCC i 111 zdravih ispitanika određene su lančanom reakcijom polimeraze i restrikcionom analizom. Logističkom regresijom procenjena je sklonost ka razvoju SCC i BCC. Rezultati. Genotip CC je utvrđen kod 15% ispitanika sa SCC, 13% sa BCC i 12% zdavih osoba. Genotip CG je zabeležen kod 41% ispitanika sa SCC, 35% sa BCC i 48% zdravih osoba. Genotip GG je otkriven kod 44% osoba sa SCC, 52% sa BCC i 40% zdravih ispitanika. Učestalost G-alela bila je sledeća: 0,65 kod ispitanika sa SCC, 0,69 kod ispitanika sa BCC i 0,64 u grupi zdravih osoba. Učestalost C-alela bila je: 0,35 kod ispitanika sa SCC, 0,31 kod ispitanika sa BCC i 0,36 u grupi zdravih osoba. Nije bilo statistički značajne razlike u raspodeli genotipova i alela između bolesnika s karcinomima i zdravih ispitanika (p>0,05). Zaključak. Polimorfizam -31G/C u promotoru gena za survivin ne može se smatrati faktorom rizika za razvoj ova dva tipa tumora.",
publisher = "Srpsko lekarsko društvo, Beograd",
journal = "Srpski arhiv za celokupno lekarstvo",
title = "Analysis of polymorphism in the survivin gene promoter as a potential risk factor for head and neck cancers development, Analiza polimorfizma u promotoru gena za survivin kao mogućeg faktora rizika za nastanak tumora glave i vrata",
volume = "141",
number = "5-6",
pages = "304-307",
doi = "10.2298/SARH1306304K"
}
Kostić, M., Nikolić, N., Ilić, B., Čarkić, J., Milenković, S.,& Vukadinović, M.. (2013). Analysis of polymorphism in the survivin gene promoter as a potential risk factor for head and neck cancers development. in Srpski arhiv za celokupno lekarstvo
Srpsko lekarsko društvo, Beograd., 141(5-6), 304-307.
https://doi.org/10.2298/SARH1306304K
Kostić M, Nikolić N, Ilić B, Čarkić J, Milenković S, Vukadinović M. Analysis of polymorphism in the survivin gene promoter as a potential risk factor for head and neck cancers development. in Srpski arhiv za celokupno lekarstvo. 2013;141(5-6):304-307.
doi:10.2298/SARH1306304K .
Kostić, Marija, Nikolić, Nadja, Ilić, Branislav, Čarkić, Jelena, Milenković, Sanja, Vukadinović, Miroslav, "Analysis of polymorphism in the survivin gene promoter as a potential risk factor for head and neck cancers development" in Srpski arhiv za celokupno lekarstvo, 141, no. 5-6 (2013):304-307,
https://doi.org/10.2298/SARH1306304K . .
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