Pregled bibliografske jedinice broj: 151998
Synthesis and antitumor activity of 5-bromo-1-mesyluracil
Synthesis and antitumor activity of 5-bromo-1-mesyluracil // XVI International Roundtable International Society of Nucleosides, Nucleotides and Nucleic Acid
Minneapolis (MN), 2004. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 151998 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Synthesis and antitumor activity of 5-bromo-1-mesyluracil
Autori
Glavaš-Obrovac, Ljubica ; Karner, Ivan ; Pavlak, Maja ; Radačić, Marko ; Kašnar-Šamprec, Jelena ; Žinić, Biserka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Skup
XVI International Roundtable International Society of Nucleosides, Nucleotides and Nucleic Acid
Mjesto i datum
Minneapolis (MN), Sjedinjene Američke Države, 12.09.2004. - 16.09.2004
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Synthesis; antitumor activity; 5-bromo-1-mesyluracil; in vitro; in vivo
Sažetak
We have prepared novel sulfonylcyclourea derivatives by attachment of sulfonyl fragment on N-1 of pyrimidine bases. The compounds showed potent growth inhibitory activity against human tumor cell lines in vitro, at concentrations of 10-5-10-8 M, and some of them showed the ability to induce apoptosis in treated tumor cells. The purpose of this study was to elucidate the effects of 5-bromo-1-(methanesulfonyl)uracil (BMsU) on the biosynthetic activity of tumor cells' enzymes involved in DNA, RNA and protein synthesis, and in de novo and salvage pyrimidine and purine syntheses. Investigations were performed in vitro on human colon carcinoma (CaCo2) and cervix carcinoma cells (HeLa). BMsU displayed inhibitory effects on DNA and RNA synthesis in CaCo2 and HeLa cells, after 24-hours of treatment. De novo biosynthesis of pyrimidine and purine was also affected in both treated tumor cell lines. Antitumor activity of BMsU is closely associated with its inhibitory activity on enzymes which play important role in the metabolism of tumor cells. The in vivo antitumor activity of BMsU was also investigated. The model used in investigations was a mouse anaplastic mammary carcinoma transplanted into the thigh of the right leg of CBA mice. Significant reduction in tumor growth time was achieved with BMsU administrated in dose of 50 mg/kg.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb,
Učiteljski fakultet, Zagreb
Profili:
Marko Radačić
(autor)
Biserka Žinić
(autor)
Ivan Karner
(autor)
Ljubica Glavaš Obrovac
(autor)