In Vivo Modulation of Angiogenic Gene Expression by Acyclic Nucleoside Phosphonates PMEDAP and PMEG

• Published in: Anticancer research 2009-04, Vol.29 (4), p.1295-1302
• Main Authors: OTOVA, Berta, HRDY, Jiri, VOTRUBA, Ivan, HOLY, Antonin
• Format: Article
• Language: English
• Subjects: Adenine - analogs & derivatives; Adenine - pharmacology; Animals; Biological and medical sciences; Epidermal Growth Factor - genetics; Epidermal Growth Factor - metabolism; Fibroblast Growth Factor 1 - genetics; Fibroblast Growth Factor 1 - metabolism; Gene Expression Regulation, Neoplastic - drug effects; Guanine - analogs & derivatives; Guanine - pharmacology; Lymphoma, T-Cell - genetics; Lymphoma, T-Cell - metabolism; Lymphoma, T-Cell - pathology; Male; Medical sciences; Neovascularization, Pathologic - metabolism; Organophosphorus Compounds - pharmacology; Platelet-Derived Growth Factor - genetics; Platelet-Derived Growth Factor - metabolism; Rats; Rats, Sprague-Dawley; Receptor, Epidermal Growth Factor - genetics; Receptor, Epidermal Growth Factor - metabolism; Receptor, Fibroblast Growth Factor, Type 1 - genetics; Receptor, Fibroblast Growth Factor, Type 1 - metabolism; Receptor, Platelet-Derived Growth Factor beta - genetics; Receptor, Platelet-Derived Growth Factor beta - metabolism; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger - genetics; RNA, Messenger - metabolism; Tumors; Vascular Endothelial Growth Factor A - genetics; Vascular Endothelial Growth Factor A - metabolism; Vascular Endothelial Growth Factor Receptor-1 - genetics; Vascular Endothelial Growth Factor Receptor-1 - metabolism
• ISSN: 0250-7005; 1791-7530

Acyclic nucleoside phosphonates PMEDAP and PMEG modulate expression of selected proangiogenic genes in SD-lymphoma bearing rats. Antiangiogenic efficacy of PMEDAP is relatively weak and is manifested mainly by down-regulation of vascular endothelial growth factor (VEGF) and its receptor VEGFR detectable 24 hours after treatment. Compound PMEG (an active metabolite of the prodrug GS-9219) down-regulates selected proangiogenic genes EGF, FGF, PDGF, VEGF, EGFR, FGFR, PDGFR and VEGFR much more efficiently. Its antiangiogenic potency persists and is more intensive 48 hours after treatment. Findings show that in vivo antitumour efficacy of both antimitotic acyclic nucleoside phosphonates PMEDAP and PMEG consequently affect the angiogenesis in T-cell lymphoma.