| Literature DB >> 33390035 |
Małgorzata Sztanke1, Jolanta Rzymowska2, Krzysztof Sztanke3.
Abstract
The main purpose of this investigation was to evaluate the effect of anticancer active compounds (I-VIII) on zebrafish development in order to select the safest molecules. Larval mortality, embryo hatchability and malformations were end-points used to assess the acute toxicity among embryos and larvae from compounds-/pemetrexed-treated and control groups. LC50 and MNLC (maximal non-lethal concentration) were determined. Lipophilicity-dependent structure-toxicity relationships were established. The results clearly indicated that the majority of test molecules are safe for zebrafish individuals and simultaneously are less toxic than an anticancer agent - pemetrexed. The subsequent aim of this study was to elucidate the molecular mechanism of antiproliferative activity of the most selective compounds. Substantially increased activation of caspase-6 and -8 in cancerous cell lines confirmed the proapoptotic action of molecules examined. Considering the safety for zebrafish individuals, the title compounds as inducers of apoptosis are promising drug candidates in the preclinical phase of drug development.Entities:
Keywords: in vivo zebrafish toxicity test; Trifluoromethylated fused triazinones; caspase activation; developmental defects; maximal non-lethal concentration; proapoptotic action; structure–toxicity relationships
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Year: 2021 PMID: 33390035 PMCID: PMC7782186 DOI: 10.1080/14756366.2020.1865944
Source DB: PubMed Journal: J Enzyme Inhib Med Chem ISSN: 1475-6366 Impact factor: 5.051