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CHARACTERIZATION OF P53 ABNORMALITIES IN B-CLL PATIENTS IN RELATION TO IGVH MUTATION STATUS AND PREVIOUS TREATMENT

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14110%2F05%3A00019164" target="_blank" >RIV/00216224:14110/05:00019164 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    CHARACTERIZATION OF P53 ABNORMALITIES IN B-CLL PATIENTS IN RELATION TO IGVH MUTATION STATUS AND PREVIOUS TREATMENT

  • Original language description

    Background: Although the defects in the p53 gene predispose B CLL patients for inferior outcome, little is known about the reasons leading to inactivation of this tumor-suppressor. The p53 abnormalities were reported to be associated with unmutated IgVHsubtype and may thus arise as a consequence of its more aggressive behaviour, but some reports point also to potentially damaging chemotherapy including alkylating agents (Sturm et al., Cell Death Differ 2003; 10: 477 to 484). Aims: The aims of the studywere to determine the spectrum of p53 mutations in B CLL patients treated or monitored at our center and to correlate the data to mutation status of IgVH and to the previous treatment. Methods: We analyzed the status of the p53 gene in 144 patients diagnosed with B CLL of all stages using functional analysis in yeasts (FASAY) supplemented by Western blotting detection of p53 protein expression and I FISH detection of p53 deletions (LSI p53 17p13.1). We used PCR and direct sequencing to

  • Czech name

    Charakterizace p53 abnormalit u B-CLL pacientů ve vztahu k mutačnímu statusu IgVH a předchozí léčbě

  • Czech description

    Background: Although the defects in the p53 gene predispose B CLL patients for inferior outcome, little is known about the reasons leading to inactivation of this tumor-suppressor. The p53 abnormalities were reported to be associated with unmutated IgVHsubtype and may thus arise as a consequence of its more aggressive behaviour, but some reports point also to potentially damaging chemotherapy including alkylating agents (Sturm et al., Cell Death Differ 2003; 10: 477 to 484). Aims: The aims of the studywere to determine the spectrum of p53 mutations in B CLL patients treated or monitored at our center and to correlate the data to mutation status of IgVH and to the previous treatment. Methods: We analyzed the status of the p53 gene in 144 patients diagnosed with B CLL of all stages using functional analysis in yeasts (FASAY) supplemented by Western blotting detection of p53 protein expression and I FISH detection of p53 deletions (LSI p53 17p13.1). We used PCR and direct sequencing to

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/NR8445" target="_blank" >NR8445: In vitro sensitivity/resistance of CLL cells with inactivated p53 on modern therapy</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2005

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Blood

  • ISSN

    0006-4971

  • e-ISSN

  • Volume of the periodical

    2005

  • Issue of the periodical within the volume

    11

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    1

  • Pages from-to

  • UT code for WoS article

  • EID of the result in the Scopus database