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In vitro investigating of anticancer activity of new 7-MEOTA-tacrine heterodimers

A combination of biochemical, biophysical and biological techniques was used to study calf thymus DNA interaction with newly synthesized 7-MEOTA-tacrine thiourea 12–17 and urea heterodimers 18–22, and to measure interference with type I and II topoisomerases. Their biological profile was also inspec...

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Detalles Bibliográficos
Autores principales: Janockova, Jana, Korabecny, Jan, Plsikova, Jana, Babkova, Katerina, Konkolova, Eva, Kucerova, Dana, Vargova, Jana, Koval, Jan, Jendzelovsky, Rastislav, Fedorocko, Peter, Kasparkova, Jana, Brabec, Viktor, Rosocha, Jan, Soukup, Ondrej, Hamulakova, Slavka, Kuca, Kamil, Kozurkova, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450562/
https://www.ncbi.nlm.nih.gov/pubmed/30938202
http://dx.doi.org/10.1080/14756366.2019.1593159
Descripción
Sumario:A combination of biochemical, biophysical and biological techniques was used to study calf thymus DNA interaction with newly synthesized 7-MEOTA-tacrine thiourea 12–17 and urea heterodimers 18–22, and to measure interference with type I and II topoisomerases. Their biological profile was also inspected in vitro on the HL-60 cell line using different flow cytometric techniques (cell cycle distribution, detection of mitochondrial membrane potential dissipation, and analysis of metabolic activity/viability). The compounds exhibited a profound inhibitory effect on topoisomerase activity (e.g. compound 22 inhibited type I topoisomerase at 1 µM concentration). The treatment of HL-60 cells with the studied compounds showed inhibition of cell growth especially with hybrids containing thiourea (14–17) and urea moieties (21 and 22). Moreover, treatment of human dermal fibroblasts with the studied compounds did not indicate significant cytotoxicity. The observed results suggest beneficial selectivity of the heterodimers as potential drugs to target cancer cells.