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
{"title":"Study of the cytotoxic/toxic potential of the novel anticancer selenodiazoloquinolone on fibroblast cells and 3D skin model.","authors":"Soňa Jantová,&nbsp;Dominika Topoľská,&nbsp;Michaela Janošková,&nbsp;Miroslav Pánik,&nbsp;Viktor Milata","doi":"10.1515/intox-2016-0014","DOIUrl":null,"url":null,"abstract":"<p><p>The new synthetically prepared quinolone derivative 7-ethyl 9-ethyl-6-oxo-6,9-dihydro[1,2,5]selenadiazolo [3,4-<i>h</i>]quinoline-7-carboxylate (E2<i>h</i>) showed in our previous study cytotoxic effects towards tumor cells and immunomodulatory activities on RAW 264.7 cell line murine macrophages. E2<i>h</i> 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<i>h</i> on human non-cancer fibroblast BHNF-1 cells and reconstructed human epidermis EpiDerm™. Further the effects of E2<i>h</i> 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.</p>","PeriodicalId":13715,"journal":{"name":"Interdisciplinary Toxicology","volume":"9 3-4","pages":"106-112"},"PeriodicalIF":0.0000,"publicationDate":"2016-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1515/intox-2016-0014","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Interdisciplinary Toxicology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/intox-2016-0014","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2017/5/17 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"Environmental Science","Score":null,"Total":0}
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.

Abstract Image

Abstract Image

Abstract Image

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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Interdisciplinary Toxicology
Interdisciplinary Toxicology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
自引率
0.00%
发文量
0
审稿时长
18 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信