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On the role of fluoro-substituted nucleosides in DNA radiosensitization for tumor radiation therapy

  • Gemcitabine (2′,2′-difluorocytidine) is a well-known radiosensitizer routinely applied in concomitant chemoradiotherapy. During irradiation of biological media with high-energy radiation secondary low-energy (<10 eV) electrons are produced that can directly induce chemical bond breakage in DNA by dissociative electron attachment (DEA). Here, we investigate and compare DEA to the three molecules 2′-deoxycytidine, 2′-deoxy-5-fluorocytidine, and gemcitabine. Fluorination at specific molecular sites, i.e., nucleobase or sugar moiety, is found to control electron attachment and subsequent dissociation pathways. The presence of two fluorine atoms at the sugar ring results in more efficient electron attachment to the sugar moiety and subsequent bond cleavage. For the formation of the dehydrogenated nucleobase anion, we obtain an enhancement factor of 2.8 upon fluorination of the sugar, whereas the enhancement factor is 5.5 when the nucleobase is fluorinated. The observed fragmentation reactions suggest enhanced DNA strand breakage induced byGemcitabine (2′,2′-difluorocytidine) is a well-known radiosensitizer routinely applied in concomitant chemoradiotherapy. During irradiation of biological media with high-energy radiation secondary low-energy (<10 eV) electrons are produced that can directly induce chemical bond breakage in DNA by dissociative electron attachment (DEA). Here, we investigate and compare DEA to the three molecules 2′-deoxycytidine, 2′-deoxy-5-fluorocytidine, and gemcitabine. Fluorination at specific molecular sites, i.e., nucleobase or sugar moiety, is found to control electron attachment and subsequent dissociation pathways. The presence of two fluorine atoms at the sugar ring results in more efficient electron attachment to the sugar moiety and subsequent bond cleavage. For the formation of the dehydrogenated nucleobase anion, we obtain an enhancement factor of 2.8 upon fluorination of the sugar, whereas the enhancement factor is 5.5 when the nucleobase is fluorinated. The observed fragmentation reactions suggest enhanced DNA strand breakage induced by secondary electrons when gemcitabine is incorporated into DNA.zeige mehrzeige weniger

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Metadaten
Verfasserangaben:Ilko BaldORCiDGND, Janina KopyraORCiD, Adrian Keller
URN:urn:nbn:de:kobv:517-opus4-73412
Schriftenreihe (Bandnummer):Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe (paper 167)
Publikationstyp:Postprint
Sprache:Englisch
Datum der Erstveröffentlichung:06.01.2014
Erscheinungsjahr:2014
Veröffentlichende Institution:Universität Potsdam
Datum der Freischaltung:13.03.2015
Freies Schlagwort / Tag:attachment; chemoradiation therapy; damage; drugs; gas-phase; low-energy electrons; molecular-mechanisms; resonant formation; single-strand breaks
Seitenanzahl:5
Erste Seite:6825
Letzte Seite:6829
Quelle:RSC Advances, 13 (2014) 4, S. 6825–6829. - DOI 10.1039/C3RA46735J
Organisationseinheiten:Mathematisch-Naturwissenschaftliche Fakultät / Institut für Chemie
DDC-Klassifikation:5 Naturwissenschaften und Mathematik / 54 Chemie / 540 Chemie und zugeordnete Wissenschaften
Peer Review:Referiert
Publikationsweg:Open Access
Lizenz (Englisch):License LogoCreative Commons - Namensnennung 3.0 Unported
Externe Anmerkung:Bibliographieeintrag der Originalveröffentlichung/Quelle
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