• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

天然生物活性苯并呋喃衍生物对MCF-7乳腺癌细胞系的高细胞毒性和凋亡作用

High Cytotoxicity and Apoptotic Effects of Natural Bioactive Benzofuran Derivative on the MCF-7 Breast Cancer Cell Line.

作者信息

Soleimani Afsane, Asadi Jahanbakhsh, Rostami-Charati Faramarz, Gharaei Roghaye

机构信息

Departments of Chemistry, Faculty of Science, Gonbad Kavous University, P.O.Box 163, Gonbad, Iran.

出版信息

Comb Chem High Throughput Screen. 2015;18(5):505-13. doi: 10.2174/1386207318666150430114815.

DOI:10.2174/1386207318666150430114815
PMID:25924658
Abstract

This study was focused on evaluation of the cytotoxicity and apoptotic affects of benzofuran derivative on MCF-7 breast cancer cell line. This effective compound was isolated from the root of Petasites hybridus plant. For experiments, the MCF-7 cells were treated with several concentrations (0-500μM) of 1-(6-hydroxy-2- isopropenyl-1-benzofuran-5-yl)-1-ethanone 1 at different times. In this study, test of neutral red was also employed for cytotoxicity assay and quantity of P53, P21. Bax genes expression was analyzed using Real-Time PCR and ELISA techniques. Results show that compound 1 has cytotoxicity and apoptotic effects on Human breast cancer (Michigan Cancer Foundation-7) MCF-7 cells.

摘要

本研究聚焦于评估苯并呋喃衍生物对MCF-7乳腺癌细胞系的细胞毒性和凋亡影响。这种有效化合物是从蜂斗菜属植物的根部分离得到的。实验中,MCF-7细胞在不同时间用几种浓度(0 - 500μM)的1-(6-羟基-2-异丙烯基-1-苯并呋喃-5-基)-1-乙酮1进行处理。在本研究中,中性红试验也用于细胞毒性测定以及P53、P21的定量分析。采用实时荧光定量PCR和酶联免疫吸附测定技术分析Bax基因的表达。结果表明,化合物1对人乳腺癌(密歇根癌症基金会-7)MCF-7细胞具有细胞毒性和凋亡作用。

相似文献

1
High Cytotoxicity and Apoptotic Effects of Natural Bioactive Benzofuran Derivative on the MCF-7 Breast Cancer Cell Line.天然生物活性苯并呋喃衍生物对MCF-7乳腺癌细胞系的高细胞毒性和凋亡作用
Comb Chem High Throughput Screen. 2015;18(5):505-13. doi: 10.2174/1386207318666150430114815.
2
Koenimbin, a natural dietary compound of Murraya koenigii (L) Spreng: inhibition of MCF7 breast cancer cells and targeting of derived MCF7 breast cancer stem cells (CD44(+)/CD24(-/low)): an in vitro study.山油柑碱,一种来自九里香(Murraya koenigii (L) Spreng)的天然膳食化合物:对MCF7乳腺癌细胞的抑制作用以及对衍生的MCF7乳腺癌干细胞(CD44(+)/CD24(-/low))的靶向作用:一项体外研究。
Drug Des Devel Ther. 2015 Feb 24;9:1193-208. doi: 10.2147/DDDT.S72127. eCollection 2015.
3
Selective cytotoxicity and modulation of apoptotic signature of breast cancer cells by Pithecellobium dulce leaf extracts.猴耳环叶提取物对乳腺癌细胞的选择性细胞毒性及凋亡特征的调节作用
Biotechnol Prog. 2016 May;32(3):756-66. doi: 10.1002/btpr.2261. Epub 2016 Apr 14.
4
Cytotoxic stilbenes from the roots of Paphiopedilum godefroyae.来自戈氏兜兰根部的细胞毒性芪类化合物。
J Asian Nat Prod Res. 2016 Dec;18(12):1143-1150. doi: 10.1080/10286020.2016.1183651. Epub 2016 Jun 16.
5
Crude Methanol Extract of Rosin Gum Exhibits Specific Cytotoxicity against Human Breast Cancer Cells via Apoptosis Induction.松香胶粗甲醇提取物通过诱导细胞凋亡特异性杀伤人乳腺癌细胞。
Anticancer Agents Med Chem. 2020;20(8):1028-1036. doi: 10.2174/1871520620666200423074826.
6
A new benzofuran derivative from Nicotiana tabacum.一种来自烟草的新型苯并呋喃衍生物。
J Asian Nat Prod Res. 2016 Aug;18(8):779-83. doi: 10.1080/10286020.2016.1145210. Epub 2016 Mar 16.
7
Dual effects of isoflavonoids from Pueraria lobata roots on estrogenic activity and anti-proliferation of MCF-7 human breast carcinoma cells.野葛根异黄酮对 MCF-7 人乳腺癌细胞雌激素活性和增殖的双重作用。
Bioorg Chem. 2019 Mar;83:135-144. doi: 10.1016/j.bioorg.2018.10.017. Epub 2018 Oct 10.
8
Synthesis of an anthraquinone derivative (DHAQC) and its effect on induction of G2/M arrest and apoptosis in breast cancer MCF-7 cell line.一种蒽醌衍生物(DHAQC)的合成及其对乳腺癌MCF-7细胞系诱导G2/M期阻滞和凋亡的作用。
Drug Des Devel Ther. 2015 Feb 17;9:983-92. doi: 10.2147/DDDT.S65468. eCollection 2015.
9
(+)-Dehydroabietylamine derivatives target triple-negative breast cancer.(+)-脱氢枞胺衍生物靶向三阴性乳腺癌。
Eur J Med Chem. 2015 Sep 18;102:9-13. doi: 10.1016/j.ejmech.2015.07.034. Epub 2015 Jul 23.
10
Molecular modeling study bioactive natural product of khellin analogues as a novel potential pharmacophore of EGFR inhibitors.分子模拟研究作为新型潜在 EGFR 抑制剂药效团的鬼臼毒素类似物的生物活性天然产物。
J Enzyme Inhib Med Chem. 2013 Dec;28(6):1171-81. doi: 10.3109/14756366.2012.719504. Epub 2012 Oct 1.

引用本文的文献

1
Structure-Activity Relationship of Benzofuran Derivatives with Potential Anticancer Activity.具有潜在抗癌活性的苯并呋喃衍生物的构效关系
Cancers (Basel). 2022 Apr 28;14(9):2196. doi: 10.3390/cancers14092196.
2
Natural source, bioactivity and synthesis of benzofuran derivatives.苯并呋喃衍生物的天然来源、生物活性及合成
RSC Adv. 2019 Sep 2;9(47):27510-27540. doi: 10.1039/c9ra04917g. eCollection 2019 Aug 29.
3
Synthesis of poly-functionalized benzofurans one-pot domino oxidation/[3+2] cyclization reactions of a hydroquinone ester and ynamides.
多官能化苯并呋喃的合成:对苯二酚酯与烯炔酰胺的一锅法多米诺氧化/[3+2]环化反应
RSC Adv. 2019 Apr 25;9(22):12567-12571. doi: 10.1039/c9ra02144b. eCollection 2019 Apr 17.
4
BL-038, a Benzofuran Derivative, Induces Cell Apoptosis in Human Chondrosarcoma Cells through Reactive Oxygen Species/Mitochondrial Dysfunction and the Caspases Dependent Pathway.BL-038,一种苯并呋喃衍生物,通过活性氧/线粒体功能障碍和半胱天冬酶依赖性途径诱导人软骨肉瘤细胞凋亡。
Int J Mol Sci. 2016 Sep 7;17(9):1491. doi: 10.3390/ijms17091491.