Browsing by Author "Radunovic, Milena (56490840800)"
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Publication Cytomegalovirus induces Interleukin-6 mediated inflammatory response in salivary gland cancer(2016) ;Radunovic, Milena (56490840800) ;Tomanovic, Nada (22941937200) ;Novakovic, Ivana (6603235567) ;Boricic, Ivan (6603959716) ;Milenkovic, Sanja (57220419015) ;Dimitrijevic, Milovan (25642808400) ;Radojevic-Skodric, Sanja (15726145200) ;Bogdanovic, Ljiljana (24167847400)Basta-Jovanovic, Gordana (6603093303)Purpose: The purpose of this study was to examine wheth er cytomegalovirus (CMV) is present in different histologi cal types of salivary gland cancer (SGC) by detecting CMV immediate-early (IE) and early gene products, and to deter mine the presence of its association with the overexpression of interleukin (IL)-6. Methods: Immunohistochemical analysis of 92 cases of dif ferent 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 tis sue 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 surround ing 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 carcinogenesis by increasing IL-6 pro duction and leading to inhibition of apoptosis and tumor development. - Some of the metrics are blocked by yourconsent settings
Publication Cytomegalovirus induces Interleukin-6 mediated inflammatory response in salivary gland cancer(2016) ;Radunovic, Milena (56490840800) ;Tomanovic, Nada (22941937200) ;Novakovic, Ivana (6603235567) ;Boricic, Ivan (6603959716) ;Milenkovic, Sanja (57220419015) ;Dimitrijevic, Milovan (25642808400) ;Radojevic-Skodric, Sanja (15726145200) ;Bogdanovic, Ljiljana (24167847400)Basta-Jovanovic, Gordana (6603093303)Purpose: The purpose of this study was to examine wheth er cytomegalovirus (CMV) is present in different histologi cal types of salivary gland cancer (SGC) by detecting CMV immediate-early (IE) and early gene products, and to deter mine the presence of its association with the overexpression of interleukin (IL)-6. Methods: Immunohistochemical analysis of 92 cases of dif ferent 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 tis sue 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 surround ing 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 carcinogenesis by increasing IL-6 pro duction and leading to inhibition of apoptosis and tumor development. - Some of the metrics are blocked by yourconsent settings
Publication Immunohistochemical study of cyclin A and p16 expression in patients with renal cell carcinoma(2017) ;Latic, Dragana (57201659994) ;Radojevic-Skodric, Sanja (15726145200) ;Nikolic, Srdjan (56427656200) ;Prvanovic, Mirjana (57201654195) ;Lazic, Miodrag (35929198300) ;Dzamic, Zoran (6506981365) ;Bogdanovic, Ljiljana (24167847400) ;Radunovic, Milena (56490840800)Vukovic, Marina (57213381743)Purpose: Renal cell carcinoma (RCC) is the most common malignant kidney tumor in adults. Dysregulation of the cell cycle can lead to cancer development. In this study, the mitosis-associated cyclin A and p16, a negative controller, were investigated as potential key points in the RCC development. Methods: This retrospective study included 74 patients with RCC. The expression of cyclin A and p16 and their correlation to histopathological parameters (TNM stage, histological subtype, nuclear grade, tumor size), gender, age, and clinical outcome were studied and analyzed. Results: The highest median value for cyclin A (40%; range 0-70)) and for p16 (57.5%; range 35-80) were found in the papillary histological subtype. Survival analysis showed that in the group of patients that had died before September 2015, the median value for cyclin A was 20% (range 0-60), which was significantly higher than 5% (range 0-70), found in the group of patients that survived (p=0.019). Conclusions: In relation to the histological subtype, the papillary type of RCC was associated with a significantly higher expression of cyclin A and p16 compared to other subtypes of RCC. High expression of cyclin A indicated worse prognosis, therefore cyclin A could be considered to be a significant prognostic marker. © 2017 Zerbinis Publications. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Immunohistochemical study of cyclin A and p16 expression in patients with renal cell carcinoma(2017) ;Latic, Dragana (57201659994) ;Radojevic-Skodric, Sanja (15726145200) ;Nikolic, Srdjan (56427656200) ;Prvanovic, Mirjana (57201654195) ;Lazic, Miodrag (35929198300) ;Dzamic, Zoran (6506981365) ;Bogdanovic, Ljiljana (24167847400) ;Radunovic, Milena (56490840800)Vukovic, Marina (57213381743)Purpose: Renal cell carcinoma (RCC) is the most common malignant kidney tumor in adults. Dysregulation of the cell cycle can lead to cancer development. In this study, the mitosis-associated cyclin A and p16, a negative controller, were investigated as potential key points in the RCC development. Methods: This retrospective study included 74 patients with RCC. The expression of cyclin A and p16 and their correlation to histopathological parameters (TNM stage, histological subtype, nuclear grade, tumor size), gender, age, and clinical outcome were studied and analyzed. Results: The highest median value for cyclin A (40%; range 0-70)) and for p16 (57.5%; range 35-80) were found in the papillary histological subtype. Survival analysis showed that in the group of patients that had died before September 2015, the median value for cyclin A was 20% (range 0-60), which was significantly higher than 5% (range 0-70), found in the group of patients that survived (p=0.019). Conclusions: In relation to the histological subtype, the papillary type of RCC was associated with a significantly higher expression of cyclin A and p16 compared to other subtypes of RCC. High expression of cyclin A indicated worse prognosis, therefore cyclin A could be considered to be a significant prognostic marker. © 2017 Zerbinis Publications. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Polymorphism of survivin -31 G/C gene are associated with risk of urothelial carcinoma in Serbian population(2017) ;Bogdanovic, Ljiljana (24167847400) ;Lazic, Miodrag (35929198300) ;Bogdanovic, Jelena (57212738158) ;Soldatovic, Ivan (35389846900) ;Nikolic, Nada (55324775800) ;Radunovic, Milena (56490840800) ;Radojevic-Skodric, Sanja (15726145200) ;Milasin, Jelena (6603015594)Basta-Jovanovic, Gordana (6603093303)Purpose: Survivin is thought to play an important role in carcinogenesis and is found to be associated with poor clinical outcome in various malignancies. Gene -31 G/C polymorphism has been identified as a risk factor for the development of several types of tumors. The purpose of this study was to investigate the association between survivin gene promoter -31C/G polymorphism and urothelial carcinoma (UC) risk in Serbian population and to compare the different expressions of survivin in UC of different disease stages, histological grades and tumor location in the upper or lower urinary tract. Methods: DNA from 94 patients with primary UC and from 82 healthy subjects was subjected to PCR restriction fragment length polymorphism analysis (PCR-RFLP) to identify individual genotypes. UC samples were subjected to immunohistochemical analysis to assess survivin expression in these lesions. Results: It was observed that the frequency of G/G genotype was greater in patients with UC (58.7%) than in controls (32%). Compared with study subjects carrying the C/G or C/C genotypes, significantly increased UC risk was found for individuals carrying the GIG genotype. Those carrying the G/G genotype had a significantly increased UC risk compared with those with C/G or C/C genotypes. Patients with UC carrying the G/G genotype had a greater prevalence of muscle-invading (stage T2-T4), high-grade (G2) tumor and immunohistochemicaly overexpressed survivin compared with those carrying the C/G or C/C genotypes. Conclusions: G/G genotype of the -31C/G polymorphism might be a risk factor for UC development. - Some of the metrics are blocked by yourconsent settings
Publication Polymorphism of survivin -31 G/C gene are associated with risk of urothelial carcinoma in Serbian population(2017) ;Bogdanovic, Ljiljana (24167847400) ;Lazic, Miodrag (35929198300) ;Bogdanovic, Jelena (57212738158) ;Soldatovic, Ivan (35389846900) ;Nikolic, Nada (55324775800) ;Radunovic, Milena (56490840800) ;Radojevic-Skodric, Sanja (15726145200) ;Milasin, Jelena (6603015594)Basta-Jovanovic, Gordana (6603093303)Purpose: Survivin is thought to play an important role in carcinogenesis and is found to be associated with poor clinical outcome in various malignancies. Gene -31 G/C polymorphism has been identified as a risk factor for the development of several types of tumors. The purpose of this study was to investigate the association between survivin gene promoter -31C/G polymorphism and urothelial carcinoma (UC) risk in Serbian population and to compare the different expressions of survivin in UC of different disease stages, histological grades and tumor location in the upper or lower urinary tract. Methods: DNA from 94 patients with primary UC and from 82 healthy subjects was subjected to PCR restriction fragment length polymorphism analysis (PCR-RFLP) to identify individual genotypes. UC samples were subjected to immunohistochemical analysis to assess survivin expression in these lesions. Results: It was observed that the frequency of G/G genotype was greater in patients with UC (58.7%) than in controls (32%). Compared with study subjects carrying the C/G or C/C genotypes, significantly increased UC risk was found for individuals carrying the GIG genotype. Those carrying the G/G genotype had a significantly increased UC risk compared with those with C/G or C/C genotypes. Patients with UC carrying the G/G genotype had a greater prevalence of muscle-invading (stage T2-T4), high-grade (G2) tumor and immunohistochemicaly overexpressed survivin compared with those carrying the C/G or C/C genotypes. Conclusions: G/G genotype of the -31C/G polymorphism might be a risk factor for UC development. - Some of the metrics are blocked by yourconsent settings
Publication The MMP-2 and MMP-9 promoter polymorphisms and susceptibility to salivary gland cancer(2016) ;Radunovic, Milena (56490840800) ;Nikolic, Nadja (55324775800) ;Milenkovic, Sanja (57220419015) ;Tomanovic, Nada (22941937200) ;Boricic, Ivan (6603959716) ;Dimitrijevic, Milovan (25642808400) ;Novakovic, Ivana (6603235567)Basta-Jovanovic, Gordana (6603093303)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. - Some of the metrics are blocked by yourconsent settings
Publication The MMP-2 and MMP-9 promoter polymorphisms and susceptibility to salivary gland cancer(2016) ;Radunovic, Milena (56490840800) ;Nikolic, Nadja (55324775800) ;Milenkovic, Sanja (57220419015) ;Tomanovic, Nada (22941937200) ;Boricic, Ivan (6603959716) ;Dimitrijevic, Milovan (25642808400) ;Novakovic, Ivana (6603235567)Basta-Jovanovic, Gordana (6603093303)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. - Some of the metrics are blocked by yourconsent settings
Publication The presence of periopathogenic bacteria in subgingival and atherosclerotic plaques– An age related comparative analysis(2018) ;Kannosh, Ibrahim (57021728600) ;Staletovic, Danijela (57196956408) ;Toljic, Bosko (55927783800) ;Radunovic, Milena (56490840800) ;Pucar, Ana (24830760200) ;Petrovic, Sanja Matic (56539393600) ;Grubisa, Ivana (55789953100) ;Lazarevic, Milos (57188650394) ;Brkic, Zlata (35104254800) ;Knezevic-Vukcevic, Jelena (57188549480)Milasin, Jelena (6603015594)Introduction: There is a known connection between periodontitis and atherosclerosis and the presence of periopathogens in blood vessels. However, changes of the oral microflora related to the aging process and its possible effects on atherosclerosis, have yet to be analyzed. The aim of this study was to assess temporal changes in the frequency of periodontal bacteria in the subgingival plaque and in atherosclerotic blood vessels of patients with atherosclerosis. Methodology:The study included 100 patients with atherosclerosis and periodontitis, divided into two groups, below and over 60 years of age. Clinical examinations were performedand subgingival plaque specimens were collected as well as biopsy specimens from the following arteries: coronary (34), carotid (29), abdominal (10), femoral (10), mammary (13) and iliac (4). Subgingival and artery specimens were subjected to PCR detection of 5 major periodontal pathogens: Porphyromonas gingivalis (Pg), Prevotella intermedia (Pi), Aggregatibacter actinomycetemcomitans (Aa), Tannerella forsythensis (Tf) and Treponema denticola (Td). Results:Tf was the most and Td the least frequent bacteria in both age groups and in both types of samples. The frequencies of bacteria in subgingival versus atherosclerotic samples were: Tf (76%:53%), Pi (71%:31%), Pg (60%:38%), Aa (39%:14%) and Td (21%:6%). Only Aa and Pi showed a significant difference of prevalence between younger and older patients. The most colonized artery was a. coronaria, followed by a. carotis, a. abdominalis, a. mammaria, and a. femoralis. Conclusions: Patient’s age and the distance of a given blood vessel from the oral cavity influenced microbiological findings in the atherotic plaque. © 2018 Kannosh et al. - Some of the metrics are blocked by yourconsent settings
Publication The presence of periopathogenic bacteria in subgingival and atherosclerotic plaques– An age related comparative analysis(2018) ;Kannosh, Ibrahim (57021728600) ;Staletovic, Danijela (57196956408) ;Toljic, Bosko (55927783800) ;Radunovic, Milena (56490840800) ;Pucar, Ana (24830760200) ;Petrovic, Sanja Matic (56539393600) ;Grubisa, Ivana (55789953100) ;Lazarevic, Milos (57188650394) ;Brkic, Zlata (35104254800) ;Knezevic-Vukcevic, Jelena (57188549480)Milasin, Jelena (6603015594)Introduction: There is a known connection between periodontitis and atherosclerosis and the presence of periopathogens in blood vessels. However, changes of the oral microflora related to the aging process and its possible effects on atherosclerosis, have yet to be analyzed. The aim of this study was to assess temporal changes in the frequency of periodontal bacteria in the subgingival plaque and in atherosclerotic blood vessels of patients with atherosclerosis. Methodology:The study included 100 patients with atherosclerosis and periodontitis, divided into two groups, below and over 60 years of age. Clinical examinations were performedand subgingival plaque specimens were collected as well as biopsy specimens from the following arteries: coronary (34), carotid (29), abdominal (10), femoral (10), mammary (13) and iliac (4). Subgingival and artery specimens were subjected to PCR detection of 5 major periodontal pathogens: Porphyromonas gingivalis (Pg), Prevotella intermedia (Pi), Aggregatibacter actinomycetemcomitans (Aa), Tannerella forsythensis (Tf) and Treponema denticola (Td). Results:Tf was the most and Td the least frequent bacteria in both age groups and in both types of samples. The frequencies of bacteria in subgingival versus atherosclerotic samples were: Tf (76%:53%), Pi (71%:31%), Pg (60%:38%), Aa (39%:14%) and Td (21%:6%). Only Aa and Pi showed a significant difference of prevalence between younger and older patients. The most colonized artery was a. coronaria, followed by a. carotis, a. abdominalis, a. mammaria, and a. femoralis. Conclusions: Patient’s age and the distance of a given blood vessel from the oral cavity influenced microbiological findings in the atherotic plaque. © 2018 Kannosh et al.
