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Browsing by Author "Basta-Jovanovic, G. (6603093303)"

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    Does the pathohistological pattern of renal biopsy change during time?
    (2018)
    Brkovic, V. (55602397800)
    ;
    Milinkovic, M. (56584187000)
    ;
    Kravljaca, M. (55354580700)
    ;
    Lausevic, M. (12776161600)
    ;
    Basta-Jovanovic, G. (6603093303)
    ;
    Marković-Lipkovski, J. (6603725388)
    ;
    Naumovic, R. (55965061800)
    Biopsy registries are one of the most important sources of accurate epidemiological data and the clinical presentation of renal diseases. A detailed analysis of clinicopathologic correlations over a period of 20 years (1987–2006) was performed earlier by our centre. The aim of this study was to check the current state and to register possible changes in clinicopathologic findings recorded under better socioeconomical circumstances and new management. Records of 665 renal biopsies performed at our institution were prospectively followed from 2007 to 2014. The results were compared with our previously published data. The average annual incidence of renal biopsies increased by 10% and included more elderly patients. Nephrotic syndrome (NS) remained the most common clinical indication for biopsy, while acute kidney injury participated more frequently than in the previous study (p < 0.001). Membranous nephropathy (MN) was still the most common cause of NS. Primary glomerulonephritis (PGN) remained the most prevalent disease, while MN was the most prevalent PGN. In comparison with the earlier period, MN was a more common diagnosis (p = 0.002), while the prevalence of mesangioproliferative non-IgA nephropathy decreased significantly during the time (p = 0.012). LN remained the most frequent secondary glomerulonephritis. The pathohistological pattern of renal biopsy remained largely unchanged during time. However, acute kidney injury was more frequently an indication for biopsy in the current study. The significant increase of biopsied elderly patients is due to the rise in their relative numbers in our population. © 2018 Elsevier GmbH
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    Does the pathohistological pattern of renal biopsy change during time?
    (2018)
    Brkovic, V. (55602397800)
    ;
    Milinkovic, M. (56584187000)
    ;
    Kravljaca, M. (55354580700)
    ;
    Lausevic, M. (12776161600)
    ;
    Basta-Jovanovic, G. (6603093303)
    ;
    Marković-Lipkovski, J. (6603725388)
    ;
    Naumovic, R. (55965061800)
    Biopsy registries are one of the most important sources of accurate epidemiological data and the clinical presentation of renal diseases. A detailed analysis of clinicopathologic correlations over a period of 20 years (1987–2006) was performed earlier by our centre. The aim of this study was to check the current state and to register possible changes in clinicopathologic findings recorded under better socioeconomical circumstances and new management. Records of 665 renal biopsies performed at our institution were prospectively followed from 2007 to 2014. The results were compared with our previously published data. The average annual incidence of renal biopsies increased by 10% and included more elderly patients. Nephrotic syndrome (NS) remained the most common clinical indication for biopsy, while acute kidney injury participated more frequently than in the previous study (p < 0.001). Membranous nephropathy (MN) was still the most common cause of NS. Primary glomerulonephritis (PGN) remained the most prevalent disease, while MN was the most prevalent PGN. In comparison with the earlier period, MN was a more common diagnosis (p = 0.002), while the prevalence of mesangioproliferative non-IgA nephropathy decreased significantly during the time (p = 0.012). LN remained the most frequent secondary glomerulonephritis. The pathohistological pattern of renal biopsy remained largely unchanged during time. However, acute kidney injury was more frequently an indication for biopsy in the current study. The significant increase of biopsied elderly patients is due to the rise in their relative numbers in our population. © 2018 Elsevier GmbH
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    Immunohistochemical detection of cyclin E in transitional cell carcinoma
    (2011)
    Bogdanovic, Ljiljana (24167847400)
    ;
    Radojevic-Skodric, S. (15726145200)
    ;
    Lazic, M. (35929198300)
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    Bogdanovic, J. (57212738158)
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    Spasic, D. (54884515100)
    ;
    Milenkovic, S. (57220419015)
    ;
    Puskas, L. (7003598901)
    ;
    Basta-Jovanovic, G. (6603093303)
    Purpose: It is known that expression disorders of cell cycle regulators play an important role in the development and prognosis of various malignant tumors. Cyclin expression changes during the cell cycle. This work aimed to analyse the expression of cyclin E in transitional cell carcinoma (TCC) and also to compare the expression of cyclin E with tumor stage and histological grade as well as to determine possible existence of differences in the expression of cyclin E in TCCs of the upper and lower urothelium. Methods: Twenty-four cases of TCC of the urinary tract were retrospectively analysed (6 cancers of the renal pelvis, 2 of the ureter and 15 of the bladder; 4 were infiltrative). Immunohistochemical staining for cyclin E of the analysed transitional cancer cells was assessed semiquantitatively: diffuse cyclin E expression + + + (> 50% of all cells), expression in larger groups of cells: + + (up to 50% of all cells), expression in individual cells or small cell clusters: + (<10% of all cells), and absence of expression. Tumor stage was based on clinical and morphological criteria. WHO classification (Lyon 2004) was used for determination of the histological grade. Results: Non-parametric Spearman's correlation showed that there was no statistically significant correlation between tumor stage and expression of cyclin E(ρ=-0331, p>0.05). Also, no statistically significant correlation between grade and the expression of cyclin E(ρ=-0077, p>0.05) was found. x 2 test results showed no statistically significant difference (x 2 = 2.136, p=0.775) in the expression of cyclin E between upper and lower urothelium. Conclusion: This study showed non significant decreased expression of cyclin E with poor differentiation, muscle invasion and upper/lower urothelium. Expression of cyclin E decreased with increasing histological grade and stage of the tumor. © 2011 Zerbinis Medical Publications.
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    Immunohistochemical detection of cyclin E in transitional cell carcinoma
    (2011)
    Bogdanovic, Ljiljana (24167847400)
    ;
    Radojevic-Skodric, S. (15726145200)
    ;
    Lazic, M. (35929198300)
    ;
    Bogdanovic, J. (57212738158)
    ;
    Spasic, D. (54884515100)
    ;
    Milenkovic, S. (57220419015)
    ;
    Puskas, L. (7003598901)
    ;
    Basta-Jovanovic, G. (6603093303)
    Purpose: It is known that expression disorders of cell cycle regulators play an important role in the development and prognosis of various malignant tumors. Cyclin expression changes during the cell cycle. This work aimed to analyse the expression of cyclin E in transitional cell carcinoma (TCC) and also to compare the expression of cyclin E with tumor stage and histological grade as well as to determine possible existence of differences in the expression of cyclin E in TCCs of the upper and lower urothelium. Methods: Twenty-four cases of TCC of the urinary tract were retrospectively analysed (6 cancers of the renal pelvis, 2 of the ureter and 15 of the bladder; 4 were infiltrative). Immunohistochemical staining for cyclin E of the analysed transitional cancer cells was assessed semiquantitatively: diffuse cyclin E expression + + + (> 50% of all cells), expression in larger groups of cells: + + (up to 50% of all cells), expression in individual cells or small cell clusters: + (<10% of all cells), and absence of expression. Tumor stage was based on clinical and morphological criteria. WHO classification (Lyon 2004) was used for determination of the histological grade. Results: Non-parametric Spearman's correlation showed that there was no statistically significant correlation between tumor stage and expression of cyclin E(ρ=-0331, p>0.05). Also, no statistically significant correlation between grade and the expression of cyclin E(ρ=-0077, p>0.05) was found. x 2 test results showed no statistically significant difference (x 2 = 2.136, p=0.775) in the expression of cyclin E between upper and lower urothelium. Conclusion: This study showed non significant decreased expression of cyclin E with poor differentiation, muscle invasion and upper/lower urothelium. Expression of cyclin E decreased with increasing histological grade and stage of the tumor. © 2011 Zerbinis Medical Publications.
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    Prognostic value of survivin expression in Wilms tumor
    (2012)
    Basta-Jovanovic, G. (6603093303)
    ;
    Radojevic-Skodric, Sanja (15726145200)
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    Brasanac, D. (6603393153)
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    Djuricic, S. (6603108728)
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    Milasin, J. (6603015594)
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    Bogdanovic, L. (24167847400)
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    Opric, D. (6506600388)
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    Savin, M. (18936901400)
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    Baralic, I. (24400806100)
    ;
    Jovanovic, M. (56490840800)
    Purpose: To determine survivin expression patterns in Wilms tumor (WT) and compare it with the expression in normal renal tissue. Also, to analyse cytoplasmic and nuclear survivin expression in relation to histological type, prognostic group and tumor stage. Methods: Immunohistochemical expression of survivin was analysed in 59 cases of primary WT and in 10 normal kidney specimens, taken from the same patients, but distant from the tumor. Results: 51 out of 59 cases of WT (86.44%) showed decreased cytoplasmic survivin expression and 4 out of 59 cases of WT (6.78%) showed nuclear overexpression of survivin. There was statistically significant difference in the frequency of decreased cytoplasmic expression of survivin in individual components of WT (p=0.005). Decreased cytoplasmic expression of survivin in epithelial, blastemal and stromal component was found significantly more often in low stage WT compared to high stage WT (Fisher exact test, p=0.0002, p=0.002, p=0.002, respectively). There was no statistically significant difference in the frequency of survivin nuclear overexpression between different stages of WT (Fisher exact test, p=0.564), histological types (Fisher exact test, p=0.915), or between different prognostic groups (Fisher exact test, p=1). Conclusion: Decreased survivin cytoplasmic expression or nuclear overexpression may be related to favorable prognosis of WT. © 2012 Zerbinis Medical Publications.
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    Prognostic value of survivin expression in Wilms tumor
    (2012)
    Basta-Jovanovic, G. (6603093303)
    ;
    Radojevic-Skodric, Sanja (15726145200)
    ;
    Brasanac, D. (6603393153)
    ;
    Djuricic, S. (6603108728)
    ;
    Milasin, J. (6603015594)
    ;
    Bogdanovic, L. (24167847400)
    ;
    Opric, D. (6506600388)
    ;
    Savin, M. (18936901400)
    ;
    Baralic, I. (24400806100)
    ;
    Jovanovic, M. (56490840800)
    Purpose: To determine survivin expression patterns in Wilms tumor (WT) and compare it with the expression in normal renal tissue. Also, to analyse cytoplasmic and nuclear survivin expression in relation to histological type, prognostic group and tumor stage. Methods: Immunohistochemical expression of survivin was analysed in 59 cases of primary WT and in 10 normal kidney specimens, taken from the same patients, but distant from the tumor. Results: 51 out of 59 cases of WT (86.44%) showed decreased cytoplasmic survivin expression and 4 out of 59 cases of WT (6.78%) showed nuclear overexpression of survivin. There was statistically significant difference in the frequency of decreased cytoplasmic expression of survivin in individual components of WT (p=0.005). Decreased cytoplasmic expression of survivin in epithelial, blastemal and stromal component was found significantly more often in low stage WT compared to high stage WT (Fisher exact test, p=0.0002, p=0.002, p=0.002, respectively). There was no statistically significant difference in the frequency of survivin nuclear overexpression between different stages of WT (Fisher exact test, p=0.564), histological types (Fisher exact test, p=0.915), or between different prognostic groups (Fisher exact test, p=1). Conclusion: Decreased survivin cytoplasmic expression or nuclear overexpression may be related to favorable prognosis of WT. © 2012 Zerbinis Medical Publications.
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    Survivin expression in odontogenic keratocysts and correlation with cytomegalovirus infection
    (2010)
    Andric, M. (20435687400)
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    Dozic, B. (6507142704)
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    Popovic, B. (7006225668)
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    Stefanovic, D. (59428781400)
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    Basta-Jovanovic, G. (6603093303)
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    Djogo, N. (33367776900)
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    Andjus, P. (6603805616)
    ;
    Milasin, J. (6603015594)
    Objectives: The aim of this study was to investigate the expression of survivin, an inhibitor of apoptosis, in odontogenic keratocysts and to compare it to the findings in non-neoplastic jaw cysts - periapical cysts, as well as to establish a possible relationship between survivin expression and human cytomegalovirus presence within these cysts. Materials and methods: Samples of 10 odontogenic keratocysts (five positive and five negative for the presence of cytomegalovirus, as determined by polymerase chain reaction) and 10 periapical cysts (five positive and five negative for the cytomegalovirus presence) were analysed. The expression of survivin was assessed by immunohistochemical methods, using monoclonal antibody that selectively recognizes the cytoplasmic form of survivin. Results: All 10 odontogenic keratocysts showed immunostaining for survivin, while all 10 periapical cysts were negative for its presence. There was no correlation between cytomegalovirus presence and expression of survivin within odontogenic keratocysts. Conclusion: Survivin may contribute to the aggressive behavior of odontogenic keratocysts, and thus support the emerging opinion of their neoplastic nature. © 2009 John Wiley & Sons A/S.
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    Survivin expression in odontogenic keratocysts and correlation with cytomegalovirus infection
    (2010)
    Andric, M. (20435687400)
    ;
    Dozic, B. (6507142704)
    ;
    Popovic, B. (7006225668)
    ;
    Stefanovic, D. (59428781400)
    ;
    Basta-Jovanovic, G. (6603093303)
    ;
    Djogo, N. (33367776900)
    ;
    Andjus, P. (6603805616)
    ;
    Milasin, J. (6603015594)
    Objectives: The aim of this study was to investigate the expression of survivin, an inhibitor of apoptosis, in odontogenic keratocysts and to compare it to the findings in non-neoplastic jaw cysts - periapical cysts, as well as to establish a possible relationship between survivin expression and human cytomegalovirus presence within these cysts. Materials and methods: Samples of 10 odontogenic keratocysts (five positive and five negative for the presence of cytomegalovirus, as determined by polymerase chain reaction) and 10 periapical cysts (five positive and five negative for the cytomegalovirus presence) were analysed. The expression of survivin was assessed by immunohistochemical methods, using monoclonal antibody that selectively recognizes the cytoplasmic form of survivin. Results: All 10 odontogenic keratocysts showed immunostaining for survivin, while all 10 periapical cysts were negative for its presence. There was no correlation between cytomegalovirus presence and expression of survivin within odontogenic keratocysts. Conclusion: Survivin may contribute to the aggressive behavior of odontogenic keratocysts, and thus support the emerging opinion of their neoplastic nature. © 2009 John Wiley & Sons A/S.
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    Time-dependent reduction of structural complexity of the buccal epithelial cell nuclei after treatment with silver nanoparticles
    (2013)
    Pantic, I. (36703123600)
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    Paunovic, J. (52464213900)
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    Perovic, M. (36543025300)
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    Cattani, C. (7004857300)
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    Pantic, S. (6507719117)
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    Suzic, S. (57193378338)
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    Nesic, D. (26023585700)
    ;
    Basta-Jovanovic, G. (6603093303)
    Recent studies have suggested that silver nanoparticles (AgNPs) may affect cell DNA structure in in vitro conditions. In this paper, we present the results indicating that AgNPs change nuclear complexity properties in isolated human epithelial buccal cells in a time-dependent manner. Epithelial buccal cells were plated in special tissue culture chamber / slides and were kept at 37°C in an RPMI 1640 cell culture medium supplemented with L-glutamine. The cells were treated with colloidal silver nanoparticles suspended in RPMI 1640 medium at the concentration 15 mg L-1. Digital micrographs of the cell nuclei in a sample of 30 cells were created at five different time steps: before the treatment (controls), immediately after the treatment, as well as 15, 30 and 60 min after the treatment with AgNPs. For each nuclear structure, values of fractal dimension, lacunarity, circularity, as well as parameters of grey level co-occurrence matrix (GLCM) texture, were determined. The results indicate time-dependent reduction of structural complexity in the cell nuclei after the contact with AgNPs. These findings further suggest that AgNPs, at concentrations present in today's over-the-counter drug products, might have significant effects on the cell genetic material. © 2013 Royal Microscopical Society.
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    Umbilical metastasis (Sister Joseph's nodule) as a first sign of a disseminated ovarian carcinoma: Comparative immunohistochemical analysis of primary tumor and its metastases
    (2005)
    Brasanac, D. (6603393153)
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    Boricic, I. (6603959716)
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    Todorovic, V. (7006326762)
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    Basta-Jovanovic, G. (6603093303)
    The case of a 46-year-old female with umbilical metastasis as a first sign of an ovarian carcinoma is reported with the results of immunohistochemical analysis of primary tumor and lymph node and umbilical metastases. All specimens were positive for cytokeratin 7, CA 125, E-cadherin, alpha-, beta-, and gamma-catenin, as well as for MSH2. Staining with cytokeratin 20 and MLH1 was negative, and Ki-67 labeled from 5% (in the center of the lesions) to over 25% (at the periphery of the lesions) of the nuclei. Beta-catenin showed membranous positivity in the central parts and absence of staining at the periphery of ovarian tumor and umbilical metastasis, whereas lymph node metastasis presented with uniform reaction throughout. The results of immunohistochemical staining could point to the mechanisms employed by malignant tumors during invasion and growth of metastasis and suggest the possible role of the microenvironment in the expression of some adhesion molecules on tumor cells. © 2005 IGCS.

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