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  • Immune response-Regulation-Congresses.  (2)
  • Multidrug resistance  (2)
  • 1
    Keywords: Lymphocyte transformation-Congresses. ; Cellular signal transduction-Congresses. ; Immune response-Regulation-Congresses. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (261 pages)
    Edition: 1st ed.
    ISBN: 9781489909879
    Series Statement: Advances in Experimental Medicine and Biology Series ; v.365
    Language: English
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  • 2
    Keywords: Immune response-Regulation-Congresses. ; Bacterial diseases-Immunological aspects-Congresses. ; Natural immunity-Congresses. ; Electronic books.
    Description / Table of Contents: Proceedings of the Seventh International Conference held in New Port Beach, California, February 6-8, 1998.
    Type of Medium: Online Resource
    Pages: 1 online resource (222 pages)
    Edition: 1st ed.
    ISBN: 9781461553557
    Series Statement: Advances in Experimental Medicine and Biology Series ; v.452
    Language: English
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  • 3
    ISSN: 1432-0843
    Keywords: Key words MRP ; Multidrug resistance ; P-glycoprotein ; Subcellular drug distribution ; Drug transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Purpose: To determine whether probenecid, an inhibitor of organic anion transport, is able to reverse multidrug resistance (MDR) through modulation of the drug transport function of MDR-associated protein (MRP) and P-glycoprotein (P-gP). Methods: Two MRP-overexpressing cell lines (HL60/AR and H69/AR) and two P-gP-overexpressing cell lines (HL60/Tax and P388/ADR) were cultured with different concentrations of daunorubicin (DNR) or vincristine (VCR) in the presence or absence of various concentrations of probenecid (0.01 – 10 mM). Drug sensitivity was determined using an MTT assay. DNR accumulation and subcellular distribution were determined by flow cytometry and confocal microscopy respectively. VCR accumulation was determined by scintillation spectrometry. Results: Probenecid, in a concentration-dependent manner, reversed resistance to DNR and VCR in HL60/AR and H69/AR tumor cell lines. This effect of probenecid on MDR was associated with an increased accumulation of DNR and VCR and correction of the altered subcellular distribution of DNR. The concentrations of probenecid that reversed MDR are clinically achievable in vivo. In contrast, probenecid did not reverse MDR in either HL60/Tax or P388/ADR tumor cell lines that overexpress P-gP. Conclusion: These results suggest that probenecid is an effective chemosensitizer of MRP-associated MDR tumor cells and is a potential candidate for clinical use to reverse MDR.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-2592
    Keywords: Multidrug resistance ; T cells ; B cells ; macrophages ; natural killer cells ; cytotoxicity ; aging ; AIDS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract P-glycoprotein, a 170-kd glycoprotein encoded by theMDR 1 gene, is a member of a highly conserved superfamily of ATP-binding cassette (ABC) transport proteins. It shares extensive homology with numerous bacterial and eukaryotic ABC transport proteins. P-glycoprotein acts as an energy-dependent efflux pump that appears to transport structurally diverse agents ranging from ions to peptides. P-glycoprotein (P-gP) has been implicated as playing a role in multidrug (MDR) resistance in cancer, chloroquine-resistantPlasmodium falciparum infection, and possibly human immunodeficiency virus-1 (HIV-1) resistance to nucleoside compounds. A number of normal tissues in humans and rodents have been shown to express high levels of P-gp. The expression and function of P-gp in cells of the immune system have been explored in the past 2 years. This review presents a state of the art regarding the expression, regulation, and function of Pgp in cells of the immune system. In addition, its alteration in aging and HIV-1 infection is reviewed. A possible physiologic role of P-gp in cytokine secretion, antigen processing/presentation, and effector functions is also discussed.
    Type of Medium: Electronic Resource
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