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Browsing by Author "Nikolic, Nada (55324775800)"

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    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.
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    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.

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