| Literature DB >> 27702608 |
Domenico Iacopetta1, Camillo Rosano2, Francesco Puoci1, Ortensia Ilaria Parisi1, Carmela Saturnino3, Anna Caruso1, Pasquale Longo4, Jessica Ceramella1, Aurélie Malzert-Fréon5, Patrick Dallemagne6, Sylvain Rault6, Maria Stefania Sinicropi7.
Abstract
Natural or synthetic carbazole derivatives have recently attracted the attention of the scientific world because of their multiple biological activity, leading to an increase of designed, synthesized and studied analogues. In this paper, four 1,4-dimethylcarbazole derivatives, analogues of Ellipticine, have been investigated for their ability to block cancer cells growth, with low effects on the proliferation of normal cells. DNA topoisomerases inhibition assays, docking simulations, stability studies and effects on a membrane model are reported. Particularly, compounds 2 and 3 have been found thermally stable and able to inhibit, strongly and selectively, the human DNA topoisomerase II. These properties confer a good and broad antitumoral activity in vitro, with very low cytotoxic effect on the proliferation of normal cell lines and without damaging, in contrast with Ellipticine, the cell membrane model. The presented outcomes set the most active compounds as good candidates for pre-clinical studies useful in cancer treatment.Entities:
Keywords: Antitumor; Docking simulation; Human topoisomerases I/II; Large unilamellar vesicles; Thermal stability
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Year: 2016 PMID: 27702608 DOI: 10.1016/j.ejps.2016.09.039
Source DB: PubMed Journal: Eur J Pharm Sci ISSN: 0928-0987 Impact factor: 4.384