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PRDM1 rs2185379, unlike BRCA1, is not a prognostic marker in patients with advanced ovarian cancer

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F24%3A10482990" target="_blank" >RIV/00216208:11110/24:10482990 - isvavai.cz</a>

  • Alternative codes found

    RIV/00064165:_____/24:10482990

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=Clg_G4XYeu" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=Clg_G4XYeu</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3233/CBM-230358" target="_blank" >10.3233/CBM-230358</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    PRDM1 rs2185379, unlike BRCA1, is not a prognostic marker in patients with advanced ovarian cancer

  • Original language description

    BACKGROUND: Ovarian cancer (OC) is mostly diagnosed in advanced stages with high incidence-to-mortality rate. Nevertheless, some patients achieve long-term disease-free survival. However, the prognostic markers have not been well established. OBJECTIVE: The primary objective of this study was to analyse the association of the suggested prognostic marker rs2185379 in PRDM1 with long-term survival in a large independent cohort of advanced OC patients. METHODS: We genotyped 545 well-characterized advanced OC patients. All patients were tested for OC predisposition. The effect of PRDM1 rs2185379 and other monitored clinicopathological and genetic variables on survival were analysed. RESULTS: The univariate analysis revealed no significant effect of PRDM1 rs2185379 on survival whereas significantly worse prognosis was observed in postmenopausal patients (HR = 2.49; 95%CI 1.90-3.26; p = 4.14 x 10(-11)) with mortality linearly increasing with age (HR = 1.05 per year; 95%CI 1.04-1.07; p = 2 x 10(-6)), in patients diagnosed with non-high-grade serous OC (HR = 0.44; 95%CI 0.32-0.60; p = 1.95 x 10(-7)) and in patients carrying a gBRCA1 pathogenic variant (HR = 0.65; 95%CI 0.48-0.87; p = 4.53 x 10(-3)). The multivariate analysis interrogating the effect of PRDM1 rs2185379 with other significant prognostic factors revealed marginal association of PRDM1 rs2185379 with worse survival in postmenopausal women (HR = 1.54; 95%CI 1.01-2.38; p = 0.046). CONCLUSIONS: Unlike age at diagnosis, OC histology or gBRCA1 status, rs2185379 in PRDM1 is unlikely a marker of long-term survival in patients with advance OC.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30101 - Human genetics

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

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

Others

  • Publication year

    2024

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Cancer Biomarkers

  • ISSN

    1574-0153

  • e-ISSN

    1875-8592

  • Volume of the periodical

    40

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    5

  • Pages from-to

    199-203

  • UT code for WoS article

    001265602500005

  • EID of the result in the Scopus database

    2-s2.0-85191968026