Pregled bibliografske jedinice broj: 510141
Synthesis and biological evaluation of 4-nitro-substituted 1, 3-diaryltriazenes as a novel class of potent antitumor agents
Synthesis and biological evaluation of 4-nitro-substituted 1, 3-diaryltriazenes as a novel class of potent antitumor agents // European journal of medicinal chemistry, 46 (2011), 7; 2971-2983 doi:10.1016/j.ejmech.2011.04.024 (međunarodna recenzija, članak, znanstveni)
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Naslov
Synthesis and biological evaluation of 4-nitro-substituted 1, 3-diaryltriazenes as a novel class of potent antitumor agents
Autori
Čimbora-Zovko, Tamara ; Brozović, Anamaria ; Piantanida, Ivo ; Fritz, Gerhard ; Virag, Andrej ; Alič, Branko ; Majce, Vita ; Kočevar, Marjan ; Polanc, Slovenko ; Osmak, Maja
Izvornik
European journal of medicinal chemistry (0223-5234) 46
(2011), 7;
2971-2983
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
1 ; 3-diaryltriazenes ; synthesis ; cytotoxicity ; ROS induction ; apoptosis
Sažetak
We describe the synthesis and biological activity of a new class of 1, 3-diaryltriazenes, namely 4-nitro-substituted 1, 3-diaryltriazenes. Structure-activity relationship analysis reveals that 1, 3-diaryltriazenes can be modified from inactive to highly cytotoxic compounds by the introduction of two nitro groups at the para positions of benzene rings and two additional electron-withdrawing groups (bromo, chloro, trifluoromethyl or fluoro substituents) at their ortho position. In order to increase the solubility of the modified compounds, we introduced various acyl groups to their triazene nitrogen. The results of LC-MS/MS analysis showed that N-acyltriazenes can be considered as prodrugs of non-acylated triazenes. Selected 3-acetyl-1, 3-bis(2-chloro-4-nitrophenyl)-1-triazene (8b) is highly cytotoxic against different tumor cell lines, including cisplatin-resistant laryngeal carcinoma cells. Notably, its antiproliferative activity is significantly higher against tumor cells than against normal cells. DNA binding analysis suggests that neither 8b nor its non-acylated derivative 8a bind into the minor groove of DNA. Instead, 8b induces reactive oxygen species that could provoke endoplasmic reticulum (ER) stress finally leading to apoptosis. Our data suggest that 4-nitro-substituted 1, 3-diaryltriazenes are a new class of anticancer molecules which preferentially target malignant cells and may serve as potential antitumor agents.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Biologija
POVEZANOST RADA
Projekti:
098-0982913-2748 - Stanični odgovor na citotoksične spojeve i razvoj otpornosti (Osmak, Maja, MZOS ) ( CroRIS)
098-0982913-2850 - Povećanje transdukcije adenovirusnih vektora i otpornost stanica na citostatike (Ambriović Ristov, Andreja, MZOS ) ( CroRIS)
098-0982914-2918 - Dizajn, sinteza i ispitivanje interakcija malih molekula s DNA, RNA i proteinima (Piantanida, Ivo, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb
Profili:
Ivo Piantanida
(autor)
Anamaria Brozović
(autor)
Maja Osmak
(autor)
Tamara Čimbora Zovko
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE