Jantová Soňa, Topoľská Dominika, Janošková Michaela, Pánik Miroslav, Milata Viktor
Institute of Biochemistry and Microbiology, Faculty of Chemical and Food Technology, Slovak University of Technology, Bratislava, Slovakia.
Institute of Experimental Pharmacology and Toxicology, Slovak Academy of Sciences, Bratislava, Slovakia.
Interdiscip Toxicol. 2016 Dec;9(3-4):106-112. doi: 10.1515/intox-2016-0014. Epub 2017 May 17.
The new synthetically prepared quinolone derivative 7-ethyl 9-ethyl-6-oxo-6,9-dihydro[1,2,5]selenadiazolo [3,4-]quinoline-7-carboxylate (E2) showed in our previous study cytotoxic effects towards tumor cells and immunomodulatory activities on RAW 264.7 cell line murine macrophages. E2 may have a potential use as a novel chemotherapeutic agent with immunomodulatory properties and the ability to induce apoptotic death of cancer cells. The aim of the present study was to examine the antiproliferative/cytotoxic activities of E2 on human non-cancer fibroblast BHNF-1 cells and reconstructed human epidermis EpiDerm™. Further the effects of E2 on tissue structure and morphology were examined. Cytotoxic/toxic studies showed that selenadiazoloquinolone is not toxic on normal human fibroblast cells BHNF-1 and dimensional skin constructs EpiDerm™. Evaluation of morphological changes in EpiDerm™ showed no change in the construction and morphology of skin tissue treated by E2h compared to control.
新合成的喹诺酮衍生物7-乙基-9-乙基-6-氧代-6,9-二氢[1,2,5]硒二唑并[3,4 - ]喹啉-7-羧酸乙酯(E2)在我们之前的研究中显示出对肿瘤细胞的细胞毒性作用以及对RAW 264.7细胞系小鼠巨噬细胞的免疫调节活性。E2可能具有作为一种新型化疗药物的潜在用途,具有免疫调节特性以及诱导癌细胞凋亡死亡的能力。本研究的目的是检测E2对人非癌成纤维细胞BHNF-1和重建人表皮EpiDerm™的抗增殖/细胞毒性活性。此外,还检测了E2对组织结构和形态的影响。细胞毒性/毒性研究表明,硒二唑并喹诺酮对正常人成纤维细胞BHNF-1和三维皮肤构建体EpiDerm™无毒。与对照相比,对EpiDerm™形态变化的评估显示,经E2处理的皮肤组织的结构和形态没有变化。