Department of Medical Chemistry, Medical University, Lublin, Poland.
Department of Biology and Genetics, Medical University, Lublin, Poland.
J Enzyme Inhib Med Chem. 2021 Dec;36(1):336-344. doi: 10.1080/14756366.2020.1865944.
The main purpose of this investigation was to evaluate the effect of anticancer active compounds () 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. LC 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.
本研究的主要目的是评估抗癌活性化合物()对斑马鱼发育的影响,以便选择最安全的分子。幼虫死亡率、胚胎孵化率和畸形率是评估化合物/培美曲塞处理组和对照组胚胎和幼虫急性毒性的终点。LC 和 MNLC(最大非致死浓度)被确定。建立了亲脂性依赖性结构-毒性关系。结果清楚地表明,大多数测试分子对斑马鱼个体是安全的,同时比抗癌药物培美曲塞的毒性更小。本研究的后续目的是阐明最具选择性的化合物的抗增殖活性的分子机制。在癌细胞系中, caspase-6 和 -8 的显著激活证实了所研究分子的促凋亡作用。考虑到对斑马鱼个体的安全性,标题化合物作为凋亡诱导剂在药物开发的临床前阶段是有前途的候选药物。