Number of the records: 1  

Glyoxalase I Glu111Ala Polymorphism in Patients with Breast Cancer

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    SYSNO ASEP0332958
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleGlyoxalase I Glu111Ala Polymorphism in Patients with Breast Cancer
    TitleGlyoxalase I Glu111Ala polymofismus u pacientů s rakovinou prsu
    Author(s) Germanová, Al. (CZ)
    Germanová, A. (CZ)
    Tesarová, P. (CZ)
    Jáchymová, M. (CZ)
    Zvára, Karel (UIVT-O)
    Zima, T. (CZ)
    Kalousová, M. (CZ)
    Source TitleCancer Investigation. - : Taylor & Francis - ISSN 0735-7907
    Roč. 27, č. 6 (2009), s. 655-660
    Number of pages6 s.
    Languageeng - English
    CountryUS - United States
    Keywordsglyoxalase I ; advanced glycation end products ; breast cancer
    Subject RIVBB - Applied Statistics, Operational Research
    CEZAV0Z10300504 - UIVT-O (2005-2011)
    UT WOS000267370700009
    DOI10.1080/07357900802350822
    AnnotationEffect of advanced glycation end products (AGEs) in the pathogenesis of cancer could be diminished by interaction with soluable RAGE or by reducing AGE-precusors via glyoxalase I. Glu111Ala polymorphism of glyoxalaseI gene, AGEs, and sRAGE serum levels were studied in 113 breast cancer patients and in 58 controls. Higher frequency of the mutated C allele was found in patients with negative estrogen receptors and in patients in clinical stage III compared to controls (P<0.05). The presence of the C allele could represent a negative prognostic factor; however, further studies are needed to confirm this hypothesis.
    WorkplaceInstitute of Computer Science
    ContactTereza Šírová, sirova@cs.cas.cz, Tel.: 266 053 800
    Year of Publishing2010
Number of the records: 1  

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