Evaluation of the Cytotoxic Effect and Antiproliferative Activity of 3-Carboxylated Coumarins Derivatives in an In Vitro Model

Cuauhtémoc Alvarado-Sánchez, A. González-González, Nancy Romero-Ceronio, E. Cruz-Hernández
{"title":"Evaluation of the Cytotoxic Effect and Antiproliferative Activity of 3-Carboxylated Coumarins Derivatives in an In Vitro Model","authors":"Cuauhtémoc Alvarado-Sánchez, A. González-González, Nancy Romero-Ceronio, E. Cruz-Hernández","doi":"10.46624/ajphr.2018.v6.i11.002","DOIUrl":null,"url":null,"abstract":"Herein we report an exploratory study based on the cytotoxicity and antiproliferative activity of four previously synthesized coumarins derivatives (compounds 1a-d). The cytotoxic effect of the compounds was assessed on mononuclear cells, which were obtained from blood samples of healthy donors and measured by XTT method. The antiproliferative activity experiments were developed using HeLa, CaSKi and SiHa cervical cancer cell lines, and was evaluated by the MTT assay. In every single experiment, Cisplatin as internal control was employed. The cytotoxic assessment revealed that the four compounds did not significantly affect the viability on normal cells, whereas the antiproliferative activity on cancer cells was variable, according to the substituent located at position 3 of the coumarin core. It is worth mentioning that compound 1c, compared with the other products, presented a remarkable effect against CaSKi cell line, likewise 1d but in HeLa cells. These findings suggest that there is a relationship between biological activity and the alkoxycarbonyl chain since this is the only structural difference among the four tested compounds. The results lead to conclude that butyl group which is the substituent in compound 1d, was the key element in the antiproliferative effect presented by the molecule against SiHa, CaSKi and HeLa cell lines.","PeriodicalId":233230,"journal":{"name":"American Journal of Pharmacy And Health Research","volume":"182 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Pharmacy And Health Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46624/ajphr.2018.v6.i11.002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Herein we report an exploratory study based on the cytotoxicity and antiproliferative activity of four previously synthesized coumarins derivatives (compounds 1a-d). The cytotoxic effect of the compounds was assessed on mononuclear cells, which were obtained from blood samples of healthy donors and measured by XTT method. The antiproliferative activity experiments were developed using HeLa, CaSKi and SiHa cervical cancer cell lines, and was evaluated by the MTT assay. In every single experiment, Cisplatin as internal control was employed. The cytotoxic assessment revealed that the four compounds did not significantly affect the viability on normal cells, whereas the antiproliferative activity on cancer cells was variable, according to the substituent located at position 3 of the coumarin core. It is worth mentioning that compound 1c, compared with the other products, presented a remarkable effect against CaSKi cell line, likewise 1d but in HeLa cells. These findings suggest that there is a relationship between biological activity and the alkoxycarbonyl chain since this is the only structural difference among the four tested compounds. The results lead to conclude that butyl group which is the substituent in compound 1d, was the key element in the antiproliferative effect presented by the molecule against SiHa, CaSKi and HeLa cell lines.
体外模型评价3-羧基香豆素衍生物的细胞毒作用和抗增殖活性
在此,我们报告了一项基于四种先前合成的香豆素衍生物(化合物1a-d)的细胞毒性和抗增殖活性的探索性研究。化合物对单个核细胞的细胞毒性作用进行了评估,这些细胞是从健康献血者的血液样本中获得的,并通过XTT法测量。用HeLa、CaSKi和SiHa宫颈癌细胞株进行抗增殖活性实验,并采用MTT法评价其抗增殖活性。单次实验均采用顺铂作为内控。细胞毒性评估显示,这四种化合物对正常细胞的活性没有显著影响,而对癌细胞的抗增殖活性则是不同的,根据位于香豆素核心位置3的取代基。值得一提的是,与其他产品相比,化合物1c对CaSKi细胞系有显著的作用,同样1d对HeLa细胞也有显著的作用。这些发现表明生物活性与烷氧羰基链之间存在关系,因为这是四种被测试化合物之间唯一的结构差异。结果表明,化合物1d中的取代基丁基是该分子抗SiHa、CaSKi和HeLa细胞株增殖作用的关键因素。
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
自引率
0.00%
发文量
0
×
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