Milenković, Sanja

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Marked epithelial to mesenchymal transition in surgical margins of oral cancer-an in vitro study

Lazarević, Miloš; Milošević, Maja; Jelovac, Drago; Milenković, Sanja; Tepavčević, Zvezdana; Baldan, Federica; Suboticki, Tijana; Toljić, Boško; Trišić, Dijana; Dragović, Miroslav; Damante, Giuseppe; Milašin, Jelena

(SPANDIDOS PUBL LTD, ATHENS, 2020)

TY  - JOUR
AU  - Lazarević, Miloš
AU  - Milošević, Maja
AU  - Jelovac, Drago
AU  - Milenković, Sanja
AU  - Tepavčević, Zvezdana
AU  - Baldan, Federica
AU  - Suboticki, Tijana
AU  - Toljić, Boško
AU  - Trišić, Dijana
AU  - Dragović, Miroslav
AU  - Damante, Giuseppe
AU  - Milašin, Jelena
PY  - 2020
UR  - https://smile.stomf.bg.ac.rs/handle/123456789/2484
AB  - Epithelial to mesenchymal transition (EMT) is a feature of several types of human cancer, including oral squamous cell carcinoma (OSCC). In the present study, tumor and margin cell cultures obtained from patients with OSCC were used to determine the expression patterns of certain EMT-associated markers, including vimentin, alpha -smooth muscle actin, SLUG and SNAIL. In addition, other EMT-associated features, including clonal, proliferative and migratory potential were compared between the two cell types. Cell cultures were generated from tumor and margin tissue samples from 6 patients and cultured up to the fifth passage. EMT marker expression was assessed by reverse transcription-quantitative PCR. Cell proliferation, colony formation and scratch wound healing assays were conducted to characterize the two cell types in terms of proliferation rates, clonality and motility. All of the studied markers were expressed in tumor and margin cells. Although no significant differences were noted with regard to the aforementioned markers, their expression tended to be higher in margin cultures than in tumor cultures. The expressions of the EMT markers were also higher in the fifth passage compared with those noted at the first with a few exceptions. The rates of proliferation and cell migration were decreased during passages, while the number of colonies was increased in both types of cell culture. Tumor and margin cells indicated certain similarities with regard to EMT transition characteristics.
PB  - SPANDIDOS PUBL LTD, ATHENS
T2  - Oncology Letters
T1  - Marked epithelial to mesenchymal transition in surgical margins of oral cancer-an in vitro study
VL  - 19
IS  - 6
SP  - 3743
EP  - 3750
DO  - 10.3892/ol.2020.11494
ER  - 
@article{
author = "Lazarević, Miloš and Milošević, Maja and Jelovac, Drago and Milenković, Sanja and Tepavčević, Zvezdana and Baldan, Federica and Suboticki, Tijana and Toljić, Boško and Trišić, Dijana and Dragović, Miroslav and Damante, Giuseppe and Milašin, Jelena",
year = "2020",
abstract = "Epithelial to mesenchymal transition (EMT) is a feature of several types of human cancer, including oral squamous cell carcinoma (OSCC). In the present study, tumor and margin cell cultures obtained from patients with OSCC were used to determine the expression patterns of certain EMT-associated markers, including vimentin, alpha -smooth muscle actin, SLUG and SNAIL. In addition, other EMT-associated features, including clonal, proliferative and migratory potential were compared between the two cell types. Cell cultures were generated from tumor and margin tissue samples from 6 patients and cultured up to the fifth passage. EMT marker expression was assessed by reverse transcription-quantitative PCR. Cell proliferation, colony formation and scratch wound healing assays were conducted to characterize the two cell types in terms of proliferation rates, clonality and motility. All of the studied markers were expressed in tumor and margin cells. Although no significant differences were noted with regard to the aforementioned markers, their expression tended to be higher in margin cultures than in tumor cultures. The expressions of the EMT markers were also higher in the fifth passage compared with those noted at the first with a few exceptions. The rates of proliferation and cell migration were decreased during passages, while the number of colonies was increased in both types of cell culture. Tumor and margin cells indicated certain similarities with regard to EMT transition characteristics.",
publisher = "SPANDIDOS PUBL LTD, ATHENS",
journal = "Oncology Letters",
title = "Marked epithelial to mesenchymal transition in surgical margins of oral cancer-an in vitro study",
volume = "19",
number = "6",
pages = "3743-3750",
doi = "10.3892/ol.2020.11494"
}
Lazarević, M., Milošević, M., Jelovac, D., Milenković, S., Tepavčević, Z., Baldan, F., Suboticki, T., Toljić, B., Trišić, D., Dragović, M., Damante, G.,& Milašin, J.. (2020). Marked epithelial to mesenchymal transition in surgical margins of oral cancer-an in vitro study. in Oncology Letters
SPANDIDOS PUBL LTD, ATHENS., 19(6), 3743-3750.
https://doi.org/10.3892/ol.2020.11494
Lazarević M, Milošević M, Jelovac D, Milenković S, Tepavčević Z, Baldan F, Suboticki T, Toljić B, Trišić D, Dragović M, Damante G, Milašin J. Marked epithelial to mesenchymal transition in surgical margins of oral cancer-an in vitro study. in Oncology Letters. 2020;19(6):3743-3750.
doi:10.3892/ol.2020.11494 .
Lazarević, Miloš, Milošević, Maja, Jelovac, Drago, Milenković, Sanja, Tepavčević, Zvezdana, Baldan, Federica, Suboticki, Tijana, Toljić, Boško, Trišić, Dijana, Dragović, Miroslav, Damante, Giuseppe, Milašin, Jelena, "Marked epithelial to mesenchymal transition in surgical margins of oral cancer-an in vitro study" in Oncology Letters, 19, no. 6 (2020):3743-3750,
https://doi.org/10.3892/ol.2020.11494 . .
9
4
9

The MMP-2 and MMP-9 promoter polymorphisms and susceptibility to salivary gland cancer

Radunović, Milena; Nikolić, Nadja; Milenković, Sanja; Tomanović, Nada; Boričić, Ivan; Dimitrijević, Milovan; Novaković, Ivana; Basta-Jovanović, Gordana

(Balkan Union of Oncology (B.U.ON.), 2016)

TY  - JOUR
AU  - Radunović, Milena
AU  - Nikolić, Nadja
AU  - Milenković, Sanja
AU  - Tomanović, Nada
AU  - Boričić, Ivan
AU  - Dimitrijević, Milovan
AU  - Novaković, Ivana
AU  - Basta-Jovanović, Gordana
PY  - 2016
UR  - https://smile.stomf.bg.ac.rs/handle/123456789/2178
AB  - Purpose: Matrix metalloproteinases (MMPs) are a family of endopeptidases that may play an important role in the development of salivary gland cancer (SGC). MMP-2 and MMP-9, members of the gelatinase protein family, are capable of degrading type IV collagen of basement membranes, and their overexpression is often associated with tumor aggressiveness and poor prognosis. The aim of this study was to establish the role of single nucleotide polymorphisms (SNPs) in MMP-2 and MMP-9 genes as putative susceptibility factors for the development of SGC. Methods: The MMP-2 -1306 C>T, MMP-2 -1575 G>A and MMP-9 -1562 C>T polymorphisms were analyzed in 93 SGC cases and 100 controls using PCR-RFLP. Results: The T allele for the MMP-2-1306 C>T polymorphism exhibited its effect in heterozygous carriers, increasing the risk for SGC (odds ratio/OR 1.98, 95% CI 1.07-3.65, p=0.03). According to the dominant model, CT+TT genotypes had a 2-fold increased risk of developing SGCs (p=0.02).When the dominant model was applied for the MMP2 -1575 G>A, individuals with GA+AA genotypes exhibited a 1.77-fold increase in cancer risk, but with borderline significance (p=0.049). Heterozygous carriers of the variant T allele for the MMP-9 -1562 C>T polymorphism had roughly a 2-fold increase in susceptibility for SGC compared to wild type homozygotes (CC) (p=0.02). Conclusion: Our findings suggest MMP-2-1306 C>T and MMP-9-1562 C>T polymorphisms genotypes seem to influence the development of SGCs, whereas MMP-2 -1575 G>A seems to be of a minor importance.
PB  - Balkan Union of Oncology (B.U.ON.)
T2  - Journal of BUON
T1  - The MMP-2 and MMP-9 promoter polymorphisms and susceptibility to salivary gland cancer
VL  - 21
IS  - 3
SP  - 597
EP  - 602
UR  - https://hdl.handle.net/21.15107/rcub_smile_2178
ER  - 
@article{
author = "Radunović, Milena and Nikolić, Nadja and Milenković, Sanja and Tomanović, Nada and Boričić, Ivan and Dimitrijević, Milovan and Novaković, Ivana and Basta-Jovanović, Gordana",
year = "2016",
abstract = "Purpose: Matrix metalloproteinases (MMPs) are a family of endopeptidases that may play an important role in the development of salivary gland cancer (SGC). MMP-2 and MMP-9, members of the gelatinase protein family, are capable of degrading type IV collagen of basement membranes, and their overexpression is often associated with tumor aggressiveness and poor prognosis. The aim of this study was to establish the role of single nucleotide polymorphisms (SNPs) in MMP-2 and MMP-9 genes as putative susceptibility factors for the development of SGC. Methods: The MMP-2 -1306 C>T, MMP-2 -1575 G>A and MMP-9 -1562 C>T polymorphisms were analyzed in 93 SGC cases and 100 controls using PCR-RFLP. Results: The T allele for the MMP-2-1306 C>T polymorphism exhibited its effect in heterozygous carriers, increasing the risk for SGC (odds ratio/OR 1.98, 95% CI 1.07-3.65, p=0.03). According to the dominant model, CT+TT genotypes had a 2-fold increased risk of developing SGCs (p=0.02).When the dominant model was applied for the MMP2 -1575 G>A, individuals with GA+AA genotypes exhibited a 1.77-fold increase in cancer risk, but with borderline significance (p=0.049). Heterozygous carriers of the variant T allele for the MMP-9 -1562 C>T polymorphism had roughly a 2-fold increase in susceptibility for SGC compared to wild type homozygotes (CC) (p=0.02). Conclusion: Our findings suggest MMP-2-1306 C>T and MMP-9-1562 C>T polymorphisms genotypes seem to influence the development of SGCs, whereas MMP-2 -1575 G>A seems to be of a minor importance.",
publisher = "Balkan Union of Oncology (B.U.ON.)",
journal = "Journal of BUON",
title = "The MMP-2 and MMP-9 promoter polymorphisms and susceptibility to salivary gland cancer",
volume = "21",
number = "3",
pages = "597-602",
url = "https://hdl.handle.net/21.15107/rcub_smile_2178"
}
Radunović, M., Nikolić, N., Milenković, S., Tomanović, N., Boričić, I., Dimitrijević, M., Novaković, I.,& Basta-Jovanović, G.. (2016). The MMP-2 and MMP-9 promoter polymorphisms and susceptibility to salivary gland cancer. in Journal of BUON
Balkan Union of Oncology (B.U.ON.)., 21(3), 597-602.
https://hdl.handle.net/21.15107/rcub_smile_2178
Radunović M, Nikolić N, Milenković S, Tomanović N, Boričić I, Dimitrijević M, Novaković I, Basta-Jovanović G. The MMP-2 and MMP-9 promoter polymorphisms and susceptibility to salivary gland cancer. in Journal of BUON. 2016;21(3):597-602.
https://hdl.handle.net/21.15107/rcub_smile_2178 .
Radunović, Milena, Nikolić, Nadja, Milenković, Sanja, Tomanović, Nada, Boričić, Ivan, Dimitrijević, Milovan, Novaković, Ivana, Basta-Jovanović, Gordana, "The MMP-2 and MMP-9 promoter polymorphisms and susceptibility to salivary gland cancer" in Journal of BUON, 21, no. 3 (2016):597-602,
https://hdl.handle.net/21.15107/rcub_smile_2178 .
12

Cytomegalovirus induces Interleukin-6 mediated inflammatory response in salivary gland cancer

Radunović, Milena; Tomanović, Nada; Novaković, Ivana; Boričić, Ivan; Milenković, Sanja; Dimitrijević, Milovan; Radojević-Škodrić, Sanja; Bogdanović, Ljiljana; Basta-Jovanović, Gordana

(Balkan Union of Oncology (B.U.ON.), 2016)

TY  - JOUR
AU  - Radunović, Milena
AU  - Tomanović, Nada
AU  - Novaković, Ivana
AU  - Boričić, Ivan
AU  - Milenković, Sanja
AU  - Dimitrijević, Milovan
AU  - Radojević-Škodrić, Sanja
AU  - Bogdanović, Ljiljana
AU  - Basta-Jovanović, Gordana
PY  - 2016
UR  - https://smile.stomf.bg.ac.rs/handle/123456789/2077
AB  - Purpose: The purpose of this study was to examine whether cytomegalovirus (CMV) is present in different histological types of salivary gland cancer (SGC) by detecting CMV immediate-early (IE) and early gene products, and to determine the presence of its association with the overexpression of interleukin (IL)-6. Methods: Immunohistochemical analysis of 92 cases of different histological types of SGC was performed to determine the presence of IL-6 and CMV antigen and its intensity in tumor tissue. Twenty samples of normal salivary gland tissue obtained during autopsy served as healthy controls. Results: CMV antigens were not found in healthy acinar tissue of salivary glands, but were expressed in epithelium of salivary gland ducts. Negative expression of CMV an tigens was also found in salivary gland tissue surrounding tumors. On the other hand, CMV was detected in 65/92 SGC cases (70.6%). Higher expression of IL-6 was found in SGC (70.7%) than in normal tissue (20%). There was a high association of CMV antigen presence with the presence of IL-6, and with the IL-6 expression intensity. Conclusions: Positive expression of CMV antigens in a high percentage of SGC cells suggests that it might play an important role in carcino genesis by increasing IL-6 production and leading to inhibition of apoptosis and tumor development.
PB  - Balkan Union of Oncology (B.U.ON.)
T2  - Journal of BUON
T1  - Cytomegalovirus induces Interleukin-6 mediated inflammatory response in salivary gland cancer
VL  - 21
IS  - 6
SP  - 1530
EP  - 1536
UR  - https://hdl.handle.net/21.15107/rcub_smile_2077
ER  - 
@article{
author = "Radunović, Milena and Tomanović, Nada and Novaković, Ivana and Boričić, Ivan and Milenković, Sanja and Dimitrijević, Milovan and Radojević-Škodrić, Sanja and Bogdanović, Ljiljana and Basta-Jovanović, Gordana",
year = "2016",
abstract = "Purpose: The purpose of this study was to examine whether cytomegalovirus (CMV) is present in different histological types of salivary gland cancer (SGC) by detecting CMV immediate-early (IE) and early gene products, and to determine the presence of its association with the overexpression of interleukin (IL)-6. Methods: Immunohistochemical analysis of 92 cases of different histological types of SGC was performed to determine the presence of IL-6 and CMV antigen and its intensity in tumor tissue. Twenty samples of normal salivary gland tissue obtained during autopsy served as healthy controls. Results: CMV antigens were not found in healthy acinar tissue of salivary glands, but were expressed in epithelium of salivary gland ducts. Negative expression of CMV an tigens was also found in salivary gland tissue surrounding tumors. On the other hand, CMV was detected in 65/92 SGC cases (70.6%). Higher expression of IL-6 was found in SGC (70.7%) than in normal tissue (20%). There was a high association of CMV antigen presence with the presence of IL-6, and with the IL-6 expression intensity. Conclusions: Positive expression of CMV antigens in a high percentage of SGC cells suggests that it might play an important role in carcino genesis by increasing IL-6 production and leading to inhibition of apoptosis and tumor development.",
publisher = "Balkan Union of Oncology (B.U.ON.)",
journal = "Journal of BUON",
title = "Cytomegalovirus induces Interleukin-6 mediated inflammatory response in salivary gland cancer",
volume = "21",
number = "6",
pages = "1530-1536",
url = "https://hdl.handle.net/21.15107/rcub_smile_2077"
}
Radunović, M., Tomanović, N., Novaković, I., Boričić, I., Milenković, S., Dimitrijević, M., Radojević-Škodrić, S., Bogdanović, L.,& Basta-Jovanović, G.. (2016). Cytomegalovirus induces Interleukin-6 mediated inflammatory response in salivary gland cancer. in Journal of BUON
Balkan Union of Oncology (B.U.ON.)., 21(6), 1530-1536.
https://hdl.handle.net/21.15107/rcub_smile_2077
Radunović M, Tomanović N, Novaković I, Boričić I, Milenković S, Dimitrijević M, Radojević-Škodrić S, Bogdanović L, Basta-Jovanović G. Cytomegalovirus induces Interleukin-6 mediated inflammatory response in salivary gland cancer. in Journal of BUON. 2016;21(6):1530-1536.
https://hdl.handle.net/21.15107/rcub_smile_2077 .
Radunović, Milena, Tomanović, Nada, Novaković, Ivana, Boričić, Ivan, Milenković, Sanja, Dimitrijević, Milovan, Radojević-Škodrić, Sanja, Bogdanović, Ljiljana, Basta-Jovanović, Gordana, "Cytomegalovirus induces Interleukin-6 mediated inflammatory response in salivary gland cancer" in Journal of BUON, 21, no. 6 (2016):1530-1536,
https://hdl.handle.net/21.15107/rcub_smile_2077 .
4

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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