Czasopismo
Tytuł artykułu
Warianty tytułu
Języki publikacji
Abstrakty
Two recently synthesized groups of acridine cytostatics containing fused heterocyclic ring(s): pyrazoloacridines (PAC) and pyrazolopyrimidoacridines (PPAC) were tested in regard to their in vitro cytotoxic activity towards a panel of sensitive and resistant human tumor cell lines. The obtained results corroborate our earlier hypothesis on the essential role of heterocyclic ring fused to the acridine moiety in the ability of acridine cytostatics to overcome multidrug resistance of tumor cells. The presence, location and kind of substituents considerably influenced both the cytotoxic activity of the derivatives and their ability to overcome multidrug resistance. The same factors also affected the cytostatics ability to differentiate between tumor cell lines with various types of drug exporting pumps.
Wydawca
Czasopismo
Rocznik
Tom
Numer
Opis fizyczny
p.87-92,fig.
Twórcy
autor
- Technical University of Gdansk, Gdansk, Poland
autor
autor
autor
Bibliografia
- 1. Dicato, M., Duhem, C., Pauly, M. & Ries, F. (1997) Multidrug resistance: Molecular and clinical aspects. Cytokines Cell. Mol. Ther. 3, 91-99.
- 2. Ling, V. (1997) Multidrug resistance: Molecular mechanisms and clinical relevance. Cancer Chemother. Pharmacol. 40(Suppl), S3-S8.
- 3. van den Heuvel-Eibrink, M.M., Sonneveld, P. & Pieters, R. (2000) The prognostic significance of membrane-transport- associated multidrug resistance (MDR) proteins in leukemia. Int. J. Clin. Pharmacol. Therapeut. 38, 94-110.
- 4. Stefanska, B., Dzieduszycka, M., Bontemps- Gracz, M.M., Borowski, E., Martelli, S., Supino, R., Pratesi, G., De Cesare, M.A., Zunino, F., Kusnierczyk, H. & Radzikowski, C. (1999) 8,11-Dihydroxy-6-[(aminoalkyl)amino]- 7 H- benzo[e]perimidin-7-ones with activity in multidrug resistant cell lines; synthesis and antitumor evaluation. J. Med. Chem. 42, 3494-3501.
- 5. Tkaczyk-Gobis, K., Tarasiuk, J., Seksek, O., Stefanska, B., Borowski, E. & Garnier- Suillerot, A. (2000) Transport of new non- cross-resistant antitumor compounds of the benzoperimidine family in multidrug resistant cells. Eur. J. Pharmacol. 413, 131-141.
- 6. Bontemps-Gracz, M.M. (2000) Aktywnosc cytotoksyczna nowych pochodnych i analogow antrachinonu oraz zwiazkow pokrewnych z grupy akrydyny ze szczegolnym uwzglednieniem komorek nowotworowych z indukowana krzyzowa opornoscia wielolekowa. (The cytotoxic activity of novel derivatives and analogues ofanthraquinone and related acridine compounds with particular emphasis on tumor cell lines with induced multidrug cross-resistance.) Ph.D. Thesis, Gdansk, 2000 (in Polish).
- 7. Antonini, I., Polucci, P. & Martelli, S. (1999) Preparation of pyrazoloacridines and pyrazolopyrimidoacridines as antitumor agents. PCT Int. Appl. WO 9906405, Chem. Abstr. 130, 153666.
- 8. Antonini, I., Polucci, P., Magnano, A. & Martelli, S. (2001) Synthesis, antitumor cytotoxicity, and DNA-binding of novel N-5,2-di- (omega -aminoalkyl)-2,6-dihydropyrazolo[3,4,5-k/j- acridine-5-carboxamides. J. Med. Chem. 44, 3329-3333.
- 9. Antonini, I., Polucci, P., Magnano, A., Gatto, B., Palumbo, M., Menta, E., Pescalli, N. & Martelli, S. (2002) 2,6- Di(omega-aminoalkyl) -2 2,5,6,7-tetrahydropyrazolo[3,4,5-mn]pyrimido- [5,6,1-de]acridine-5,7-diones: Novel, potent, cytotoxic, and DNA-binding agents . J. Med. Chem. (in press).
Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.agro-article-3f74c45b-e9b2-4b71-8367-9036421ce3cc