Pregled bibliografske jedinice broj: 424335
Mechanism of action of three novel dicationic bis(phenylamidine) derivatives
Mechanism of action of three novel dicationic bis(phenylamidine) derivatives // The FEBS Journal
Prag, Češka Republika, 2009. str. 328-328 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 424335 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Mechanism of action of three novel dicationic bis(phenylamidine) derivatives
Autori
Mišković, Katarina ; Stolić, Ivana ; Piantanida, Ivo ; Baus Lončar, Mirela ; Bajić, Miroslav ; Glavaš-Obrovac, Ljubica
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
The FEBS Journal
/ - , 2009, 328-328
Skup
34th FEBS Congress: Life's Molecular Interactions
Mjesto i datum
Prag, Češka Republika, 04.07.2009. - 09.07.2009
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
DNA- minor groove binder; Hoechst 33258; bis(phenylamidine) derivatives; antiproliferative effects; cell cycle; HeLa cells
Sažetak
Three novel DNA minor groove binders: 2, 5-bis(4-amidinophenyl)-3, 4-ethylenedioxy-thiophene dihydrochloride (1), 2, 5-bis[4-(N-isopropylamidino)phenyl)]-3, 4-ethylene-dioxythiophene dihydrochloride (2) and 2, 5-bis[4-(2-imidazolino)phenyl]-3, 4-ethylene-dioxythiophene dihydrochloride (3) have been synthesized and evaluated for antiproliferative activity.According to the UV/vis titrations compounds 1-3 show high affinity (Ks > 105 M– 1) toward ds-DNA, and accordingly cause strong thermal stabilisation of DNA ( Tm > 12 °C). For all studied compounds circular dichroism (CD) titrations strongly support DNA minor groove binding as a dominant interaction. Furthermore, compounds 1-3 and DNA- minor groove binder Hoechst 33258, at concentration of 10-4 to 10-7 M, were tested against panel of 7 solid tumour cell lines (MCF-7, NCI-H358, CaCo-2, HEp-2, HeLa, AGS, and MiaPaCa). Compound 3 exhibits the best antiproliferative efficiency at all tested doses compared to control. By monitoring internalization dynamics we notice that compound 3 penetrates in to the live HeLa cell and localises in to the nucleus after 90 minutes of incubation. Cell cycle analysis showed that compound 3 at equitoxic concentration (5*10– 5 M) arrested HeLa cells in G1 and G2/M phases at all 3 tested times (24, 48, 72 h) at statistically significant level (p < 0.05), at variance to the effect observed for Hoechst 33258, which stopped cell cycle in S phase under the same conditions.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija, Temeljne medicinske znanosti
POVEZANOST RADA
Projekti:
053-0982914-2965 - Dizajn i sinteza bisamidina sa protutumorskim djelovanjem (Bajić, Miroslav, MZOS ) ( CroRIS)
098-0982914-2918 - Dizajn, sinteza i ispitivanje interakcija malih molekula s DNA, RNA i proteinima (Piantanida, Ivo, MZOS ) ( CroRIS)
219-0982914-2176 - Mehanizam bioloških učinaka novih malih molekula na stanice tumora čovjeka (Glavaš Obrovac, Ljubica, MZOS ) ( CroRIS)
219-0982914-2179 - Uloga malih zaštitinih TFF proteina u zdravlju i bolesti (Belovari, Tatjana, MZOS ) ( CroRIS)
Ustanove:
Veterinarski fakultet, Zagreb,
Institut "Ruđer Bošković", Zagreb,
Klinički bolnički centar Osijek,
Medicinski fakultet, Osijek
Profili:
Ivo Piantanida
(autor)
Miroslav Bajić
(autor)
Katarina Mišković Špoljarić
(autor)
Mirela Baus Lončar
(autor)
Ljubica Glavaš Obrovac
(autor)
Ivana Stolić
(autor)