Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/20759
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dc.contributor.authorPipili-Synetos, E.en
dc.contributor.authorPapageorgiou, A.en
dc.contributor.authorSakkoula, E.en
dc.contributor.authorSotiropoulou, G.en
dc.contributor.authorFotsis, T.en
dc.contributor.authorKarakiulakis, G.en
dc.contributor.authorMaragoudakis, M. E.en
dc.date.accessioned2015-11-24T19:09:52Z-
dc.date.available2015-11-24T19:09:52Z-
dc.identifier.issn0007-1188-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/20759-
dc.rightsDefault Licence-
dc.subjectAnimalsen
dc.subjectCarcinoma/*drug therapyen
dc.subjectCattleen
dc.subjectCells, Cultured/drug effectsen
dc.subjectDisease Models, Animalen
dc.subjectDose-Response Relationship, Drugen
dc.subjectHumansen
dc.subjectIsosorbide Dinitrate/*analogs & derivatives/metabolism/pharmacologyen
dc.subjectMaleen
dc.subjectMiceen
dc.subjectNeoplasm Metastasisen
dc.subjectNeovascularization, Pathologic/*drug therapyen
dc.subjectNitric Oxide/metabolismen
dc.subjectRabbitsen
dc.subjectVasodilator Agents/*metabolism/*pharmacologyen
dc.titleInhibition of angiogenesis, tumour growth and metastasis by the NO-releasing vasodilators, isosorbide mononitrate and dinitrateen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/8528567-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate1995-
heal.abstract1. The effect of the nitric oxide (NO)-producing nitrovasodilators isosorbide mononitrate (ISMN) and isosorbide dinitrate (ISDN) were assessed on (a) the in vivo model of angiogenesis of the chick chorioallantoic membrane (CAM) and (b) on the growth and metastatic properties of the Lewis Lung carcinoma (LLC) in mice. 2. Isosorbide 5-mononitrate (ISMN) and isosorbide dinitrate (ISDN), inhibited angiogenesis in the CAM dose-dependently. ISMN was more potent in inhibiting this process. Both compounds were capable of completely reversing the angiogenic effect of alpha-thrombin. These effects of ISMN and ISDN on angiogenesis were comparable to those previously observed with sodium nitroprusside which generates NO non-enzymatically. 3. Mice, implanted intramuscularly with LLC, received daily i.p. injections of ISMN for 14 days resulting in a significant decrease in the size of the primary tumour and a reduction in the number and size of metastatic foci in the lungs. ISDN had a similar but less pronounced effect than that observed with ISMN. 4. Addition of ISMN or ISDN to cultures of bovine, rabbit and human endothelial cells and to cultures of LLC cells had no effect on their growth characteristics. 5. These results indicate that ISMN and ISDN inhibit angiogenesis and tumor growth and metastasis in an animal tumour model. The possibility should therefore be considered that these nitrovasodilators which are widely used therapeutically and have well characterized pharmacological profiles, may also possess antitumour properties in the clinic.en
heal.journalNameBr J Pharmacolen
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά)

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