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  • PGE2-dependent CXCL12 production and CXCR4 expression control the accumulation of human MDSCs in ovarian cancer environment
    Obermajer, Nataša ...
    Signals mediated by CXCL12 (SDF1) and its receptor CXCR4 are centrally involved in cancer progression, both directly by activating cancer cells and indirectly by inducing angiogenesis plus recruiting ... T regulatory and plasmacytoid dendritic immune cells. Here we show that in ascites isolated from ovarian cancer patients, both CXCL12 and CXCR4 are controlled by the tumor-associated inflammatory mediator prostaglandin E2 (PGE2), which attractsmyeloid-derived suppressor cells (MDSC) into the ascites micro environment. In this setting, PGE2 was essential both for expression of functional CXCR4 in cancer-associated MDSCs and for production of its ligand CXCL12. Frequencies of CD11b+CD14+CD33+CXCR4+ MDSCs closely correlated with CXCL12 and PGE2 levels in patient ascites. MDSCs migrated towards OvCa ascites in a CXCR4-dependent manner that required COX2 activity and autocrine PGE2 production. Inhibition of COX2 or the PGE2 receptors EP2/EP4 in MDSCs suppressed expression of CXCR4 and MDSC responsiveness to CXCL12 or OvCa ascites. Similarly, COX2 inhibition also blocked CXCL12 production in the OvCa environment and its ability to attract MDSCs. Together, our findings elucidate a central role for PGE2 in MDSC accumulation triggered by the CXCL12-CXCR4 pathway, providing a powerful rationale to target PGE2 signaling in OvCa therapy.
    Vir: Cancer research. - ISSN 0008-5472 (Vol. 71, no. 24, 2011, str. 7463-7470)
    Vrsta gradiva - članek, sestavni del
    Leto - 2011
    Jezik - angleški
    COBISS.SI-ID - 3141745

    Povezava(-e):

    http://cancerres.aacrjournals.org/content/early/2011/10/21/0008-5472.CAN-11-2449.long
    DOI

vir: Cancer research. - ISSN 0008-5472 (Vol. 71, no. 24, 2011, str. 7463-7470)
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