Δημοσίευση

Safety and efficacy of suicide gene therapy with adenosine deaminase 5-fluorocytosine silmutaneously in in vitro cultures of melanoma and retinal cell lines.

ΤίτλοςSafety and efficacy of suicide gene therapy with adenosine deaminase 5-fluorocytosine silmutaneously in in vitro cultures of melanoma and retinal cell lines.
Publication TypeJournal Article
Year of Publication2014
AuthorsSakkas, A., Zarogoulidis P., Domvri K., Hohenforst-Schmidt W., Bougiouklis D., Kakolyris S., Zarampoukas T., Kioumis I., Pitsiou G., Huang H., Li Q., Meditskou S., Tsiouda T., Pezirkianidis N., & Zarogoulidis K.
JournalJ Cancer
Volume5
Issue5
Pagination368-81
Date Published2014
ISSN1837-9664
Abstract

Local treatment as a treatment modality is gaining increased general acceptance over time. Novel drugs and methodologies of local administration are being investigated in an effort to achieve disease local control. Suicide gene therapy is a method that has been investigated as a local treatment with simultaneously distant disease control. In our current experiment we purchased HTB-70 (melanoma cell line, derived from metastatic axillary node) and CRL-2302 (human retinal epithelium) were from ATCC LGC Standards and Ancotil(®), 2.5 g/250 ml (1 g/00ml) (5-Flucytosine) MEDA; Pharmaceuticals Ltd. UK. Adenosine Cytosine Deaminase (Ad.CD) was also used in order to convert the pro-drug 5-Flucytosine to the active 5-Fluoracil. Three different concentrations of 5-Flucytosine (5-FC) were administered (0.2ml, 0.8ml and 1.2ml). At indicated time-points (4h, 8h and 24h) cell viability and apoptosis were measured. Our concept was to investigate whether suicide gene therapy with Ad. CD-5-FC could be used with safety and efficiency as a future local treatment for melanoma located in the eye cavity. Indeed, our results indicated that in every 5-FC administration had mild cytotoxicity for the retinal cells, while increased apoptosis was observed for the melanoma cell line.

DOI10.7150/jca.9147
Alternate JournalJ Cancer
PubMed ID24799955
PubMed Central IDPMC4007525

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