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1000 Titel
  • Apoptotic and anti-proliferative effect of guanosine and guanosine derivatives in HuT-78 T lymphoma cells
1000 Autor/in
  1. Schneider, Erich H. |
  2. Hofmeister, Olga |
  3. Kälble, Solveig |
  4. Seifert, Roland |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-04-20
1000 Erschienen in
1000 Quellenangabe
  • 393(7):1251-1267
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00210-020-01864-8 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7314729/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • The effects of 100 μM of 3',5'-cGMP, cAMP, cCMP, and cUMP as well as of the corresponding membrane-permeant acetoxymethyl esters on anti-CD3-antibody (OKT3)-induced IL-2 production of HuT-78 cutaneous T cell lymphoma (Sézary lymphoma) cells were analyzed. Only 3',5'-cGMP significantly reduced IL-2 production. Flow cytometric analysis of apoptotic (propidium iodide/annexin V staining) and anti-proliferative (CFSE staining) effects revealed that 3',5'-cGMP concentrations > 50 μM strongly inhibited proliferation and promoted apoptosis of HuT-78 cells (cultured in the presence of αCD3 antibody). Similar effects were observed for the positional isomer 2',3'-cGMP and for 2',-GMP, 3'-GMP, 5'-GMP, and guanosine. By contrast, guanosine and guanosine-derived nucleotides had no cytotoxic effect on peripheral blood mononuclear cells (PBMCs) or acute lymphocytic leukemia (ALL) xenograft cells. The anti-proliferative and apoptotic effects of guanosine and guanosine-derived compounds on HuT-78 cells were completely eliminated by the nucleoside transport inhibitor NBMPR (S-(4-Nitrobenzyl)-6-thioinosine). By contrast, the ecto-phosphodiesterase inhibitor DPSPX (1,3-dipropyl-8-sulfophenylxanthine) and the CD73 ecto-5'-nucleotidase inhibitor AMP-CP (adenosine 5'-(α,β-methylene)diphosphate) were not protective. We hypothesize that HuT-78 cells metabolize guanosine-derived nucleotides to guanosine by yet unknown mechanisms. Guanosine then enters the cells by an NBMPR-sensitive nucleoside transporter and exerts cytotoxic effects. This transporter may be ENT1 because NBMPR counteracted guanosine cytotoxicity in HuT-78 cells with nanomolar efficacy (IC
1000 Sacherschließung
lokal Guanosine
lokal Leukocytes, Mononuclear/drug effects [MeSH]
lokal Cell Line, Tumor [MeSH]
lokal Humans [MeSH]
lokal Precursor Cell Lymphoblastic Leukemia-Lymphoma/pathology [MeSH]
lokal Apoptosis/drug effects [MeSH]
lokal Apoptosis
lokal T-cells
lokal Nucleoside transporters
lokal Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy [MeSH]
lokal Lymphoma, T-Cell/drug therapy [MeSH]
lokal Original Article
lokal Guanosine/administration
lokal Xenograft Model Antitumor Assays [MeSH]
lokal Nucleoside Transport Proteins/metabolism [MeSH]
lokal Lymphoma, T-Cell/pathology [MeSH]
lokal Proliferation
lokal Inhibitory Concentration 50 [MeSH]
lokal Guanosine/pharmacology [MeSH]
lokal Leukemia
lokal Guanosine/analogs
lokal Cell Proliferation/drug effects [MeSH]
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/U2NobmVpZGVyLCBFcmljaCBILg==|https://frl.publisso.de/adhoc/uri/SG9mbWVpc3RlciwgT2xnYQ==|https://frl.publisso.de/adhoc/uri/S8OkbGJsZSwgU29sdmVpZw==|https://frl.publisso.de/adhoc/uri/U2VpZmVydCwgUm9sYW5k
1000 Hinweis
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1000 @id frl:6466384.rdf
1000 Erstellt am 2023-11-16T22:44:42.026+0100
1000 Erstellt von 322
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1000 Zuletzt bearbeitet Fri Dec 01 04:09:27 CET 2023
1000 Objekt bearb. Fri Dec 01 04:09:27 CET 2023
1000 Vgl. frl:6466384
1000 Oai Id
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