Study of the cytotoxic/toxic potential of the novel anticancer selenodiazoloquinolone on fibroblast cells and 3D skin model.

Q3 Environmental Science Interdisciplinary Toxicology Pub Date : 2016-12-01 Epub Date: 2017-05-17 DOI:10.1515/intox-2016-0014
Soňa Jantová, Dominika Topoľská, Michaela Janošková, Miroslav Pánik, Viktor Milata
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引用次数: 7

Abstract

The new synthetically prepared quinolone derivative 7-ethyl 9-ethyl-6-oxo-6,9-dihydro[1,2,5]selenadiazolo [3,4-h]quinoline-7-carboxylate (E2h) showed in our previous study cytotoxic effects towards tumor cells and immunomodulatory activities on RAW 264.7 cell line murine macrophages. E2h 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 E2h on human non-cancer fibroblast BHNF-1 cells and reconstructed human epidermis EpiDerm™. Further the effects of E2h 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.

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新型抗癌药物硒代二氮唑喹诺酮对成纤维细胞和3D皮肤模型的细胞毒/毒性潜力研究。
新合成的喹诺酮衍生物7-乙基- 9-乙基-6-氧-6,9-二氢[1,2,5]硒二唑[3,4-h]喹诺酮-7-羧酸盐(E2h)在我们前期的研究中显示出对肿瘤细胞的细胞毒作用和对小鼠RAW 264.7细胞系巨噬细胞的免疫调节活性。E2h可能作为一种具有免疫调节特性和诱导癌细胞凋亡能力的新型化疗药物具有潜在的用途。本研究的目的是检测E2h对人非癌成纤维细胞BHNF-1细胞和重建的人表皮表皮的抗增殖/细胞毒活性。进一步观察了E2h对组织结构和形态的影响。细胞毒/毒性研究表明,硒二氮唑喹诺酮对正常人成纤维细胞BHNF-1和尺寸皮肤构建物EpiDerm™无毒。表皮™的形态学变化评估显示,与对照组相比,E2h处理的皮肤组织的结构和形态没有变化。
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Interdisciplinary Toxicology
Interdisciplinary Toxicology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
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