Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/3700
Title: Antiproliferative and antimigratory effects of 3-(4-substituted benzyl)-5- isopropyl-5-phenylhydantoin derivatives in human breast cancer cells
Authors: Obradović, Ana
Matić, Miloš
Ognjanović, Branka
Đurđević, Predrag
Marinković, Emilija
Ušćumlić, Gordana
Božić, Bojan 
Božić Nedeljković, Biljana 
Keywords: Apoptosis;Breast cancer cell line MDA-MB-231;Cell motility;Hydantoin derivatives;Nitric oxide;Proliferation
Issue Date: Mar-2020
Rank: M21
Citation: Obradović A, Matić M, Ognjanović B, Đurđević P, Marinković E, Ušćumlić G, Božić B, Božić Nedeljković B. Antiproliferative and antimigratory effects of 3-(4-substituted benzyl)-5- isopropyl-5-phenylhydantoin derivatives in human breast cancer cells. Saudi Pharm J. 2020 Mar;28(3):246-254. doi: 10.1016/j.jsps.2020.01.003. Epub 2020 Jan 24. PMID: 32194325; PMCID: PMC7078530.
Journal: Saudi Pharmaceutical Journal
Abstract: 
In this study, a series of synthesized 3-(4-substituted benzyl)-5-isopropyl-5-phenylhydantoin derivatives as a potential antiproliferative and antimigratory agents were investigated. The possible antitumor mechanisms of investigated hydantoin derivatives were examined on human breast cancer cell line MDA-MB-231. The cells were treated with different concentrations of compounds (from 0.01 µM to 100 µM) during 24 h and 72 h. The proliferation index, nitric oxide production, apoptosis rate, and migration capacity were measured. The cell invasion potential was examined by measuring the level of MMP-9 and COX-2 gene expression. All tested compounds expressed antiproliferative activity and induced dose- and time-dependent increase in the level of nitrites. The investigated molecules significantly decreased cell survival rate, migration capacity and the expression levels of genes included in the process of tumor invasion. Obtained data suggest that the tested hydantoin derivatives express considerable antitumor activity by reducing cell division rate, elevating apoptosis level, and inhibiting the motility and invasiveness of breast cancer cells. The results obtained in this study indicate that investigated compounds express potential as a novel chemotherapeutic agents against breast cancer growth and progression.
URI: https://biore.bio.bg.ac.rs/handle/123456789/3700
ISSN: 1319-0164
DOI: 10.1016/j.jsps.2020.01.003
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