• 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

异佛手柑内酯对乳腺癌和前列腺癌细胞系的抗增殖评估。

Antiproliferative evaluation of isofuranodiene on breast and prostate cancer cell lines.

作者信息

Buccioni Michela, Dal Ben Diego, Lambertucci Catia, Maggi Filippo, Papa Fabrizio, Thomas Ajiroghene, Santinelli Claudia, Marucci Gabriella

机构信息

School of Pharmacy, Medicinal Chemistry Unit, University of Camerino, Via S. Agostino 1 62032 Camerino, Italy.

出版信息

ScientificWorldJournal. 2014;2014:264829. doi: 10.1155/2014/264829. Epub 2014 May 22.

DOI:10.1155/2014/264829
PMID:24967427
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4055639/
Abstract

The anticancer activity of isofuranodiene, extracted from Smyrnium olusatrum, was evaluated in human breast adenocarcinomas MDA-MB 231 and BT 474, and Caucasian prostate adenocarcinoma PC 3 cell lines by MTS assay. MTS assay showed a dose-dependent growth inhibition in the tumor cell lines after isofuranodiene treatment. The best antiproliferative activity of the isofuranodiene was found on PC 3 cells with an IC50 value of 29 μM, which was slightly less than the inhibition against the two breast adenocarcinoma cell lines with IC50 values of 59 and 55 μM on MDA-MB 231 and BT 474, respectively. Hoechst 33258 assay was performed in order to study the growth inhibition mechanism in prostate cancer cell line; the results indicate that isofuranodiene induces apoptosis. Overall, the understudy compound has a good anticancer activity especially towards the PC 3. On the contrary, it is less active on Chinese hamster ovary cells (CHO) and human embryonic kidney (HEK 293) appearing as a good candidate as a potential natural anticancer drug with low side effects.

摘要

采用MTS法,对从香芹中提取的异呋喃二烯在人乳腺腺癌MDA - MB 231和BT 474以及高加索人前列腺腺癌PC 3细胞系中的抗癌活性进行了评估。MTS法显示,异呋喃二烯处理后,肿瘤细胞系的生长受到剂量依赖性抑制。异呋喃二烯对PC 3细胞的抗增殖活性最佳,IC50值为29 μM,略低于对两种乳腺腺癌细胞系的抑制作用,MDA - MB 231和BT 474的IC50值分别为59 μM和55 μM。为研究前列腺癌细胞系的生长抑制机制,进行了Hoechst 33258检测;结果表明异呋喃二烯可诱导细胞凋亡。总体而言,所研究的化合物具有良好的抗癌活性,尤其是对PC 3细胞。相反,它对中国仓鼠卵巢细胞(CHO)和人胚肾细胞(HEK 293)的活性较低,有望成为一种潜在的低副作用天然抗癌药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a115/4055639/0490fc76a736/TSWJ2014-264829.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a115/4055639/eb09b6a39358/TSWJ2014-264829.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a115/4055639/788833911b82/TSWJ2014-264829.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a115/4055639/6ca1f68a6e35/TSWJ2014-264829.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a115/4055639/5dca7f23d28e/TSWJ2014-264829.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a115/4055639/0490fc76a736/TSWJ2014-264829.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a115/4055639/eb09b6a39358/TSWJ2014-264829.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a115/4055639/788833911b82/TSWJ2014-264829.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a115/4055639/6ca1f68a6e35/TSWJ2014-264829.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a115/4055639/5dca7f23d28e/TSWJ2014-264829.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a115/4055639/0490fc76a736/TSWJ2014-264829.005.jpg

相似文献

1
Antiproliferative evaluation of isofuranodiene on breast and prostate cancer cell lines.异佛手柑内酯对乳腺癌和前列腺癌细胞系的抗增殖评估。
ScientificWorldJournal. 2014;2014:264829. doi: 10.1155/2014/264829. Epub 2014 May 22.
2
Stabilization of the cyclodecadiene derivative isofuranodiene by silver (I) coordination. Mechanistic and biological aspects.通过银(I)配位实现环癸二烯衍生物异佛尔酮二烯的稳定化:机理与生物学方面
Fitoterapia. 2017 Mar;117:52-60. doi: 10.1016/j.fitote.2016.12.009. Epub 2017 Jan 6.
3
Isofuranodiene: A neuritogenic compound isolated from wild celery (Smyrnium olusatrum L., Apiaceae).异呋喃二烯:一种从野生芹菜(香根芹,伞形科)中分离出的促神经突生长化合物。
Food Chem. 2016 Feb 1;192:782-7. doi: 10.1016/j.foodchem.2015.07.079. Epub 2015 Jul 21.
4
Wild celery (Smyrnium olusatrum L.) oil and isofuranodiene induce apoptosis in human colon carcinoma cells.野芹菜(欧洲没药树)油和异呋喃二烯可诱导人结肠癌细胞凋亡。
Fitoterapia. 2014 Sep;97:133-41. doi: 10.1016/j.fitote.2014.06.004. Epub 2014 Jun 9.
5
Synthesis and Evaluation of 2-Naphthaleno trans-Stilbenes and Cyanostilbenes as Anticancer Agents.2-萘基反式二苯乙烯和氰基二苯乙烯作为抗癌剂的合成与评价
Anticancer Agents Med Chem. 2018;18(4):556-564. doi: 10.2174/1871521409666170412115703.
6
Isofuranodiene synergizes with temozolomide in inducing glioma cells death.异呋喃二烯与替莫唑胺协同诱导神经胶质瘤细胞死亡。
Phytomedicine. 2019 Jan;52:51-59. doi: 10.1016/j.phymed.2018.09.220. Epub 2018 Sep 26.
7
Design, synthesis and apoptosis inducing effect of novel (Z)-3-(3'-methoxy-4'-(2-amino-2-oxoethoxy)-benzylidene)indolin-2-ones as potential antitumour agents.新型(Z)-3-(3'-甲氧基-4'-(2-氨基-2-氧代乙氧基)-亚苄基)-吲哚啉-2-酮的设计、合成及诱导细胞凋亡作用研究作为潜在的抗肿瘤药物。
Eur J Med Chem. 2016 Aug 8;118:34-46. doi: 10.1016/j.ejmech.2016.04.025. Epub 2016 Apr 11.
8
Glycophenotype of breast and prostate cancer stem cells treated with thieno[2,3-]pyridine anticancer compound.用噻吩并[2,3-]吡啶抗癌化合物处理的乳腺癌和前列腺癌干细胞的糖表型
Drug Des Devel Ther. 2017 Mar 14;11:759-769. doi: 10.2147/DDDT.S121122. eCollection 2017.
9
Nanostructured liquid crystalline particles as delivery vectors for isofuranodiene: Characterization and in-vitro anticancer activity.纳米结构液晶颗粒作为异佛尔二烯的递送载体:表征及体外抗癌活性
Colloids Surf B Biointerfaces. 2020 Aug;192:111050. doi: 10.1016/j.colsurfb.2020.111050. Epub 2020 Apr 18.
10
Cellular effect of styrene substituted biscoumarin caused cellular apoptosis and cell cycle arrest in human breast cancer cells.苯乙烯取代双香豆素的细胞效应导致人乳腺癌细胞发生细胞凋亡和细胞周期阻滞。
Int J Biochem Cell Biol. 2017 Nov;92:104-114. doi: 10.1016/j.biocel.2017.09.019. Epub 2017 Sep 25.

引用本文的文献

1
Screening fructosamine-3-kinase (FN3K) inhibitors, a deglycating enzyme of oncogenic Nrf2: Human FN3K homology modelling, docking and molecular dynamics simulations.筛选果糖胺-3-激酶(FN3K)抑制剂,一种致癌 Nrf2 的去糖基化酶:人 FN3K 同源建模、对接和分子动力学模拟。
PLoS One. 2023 Nov 1;18(11):e0283705. doi: 10.1371/journal.pone.0283705. eCollection 2023.
2
Ion Channels and Transporters as Therapeutic Agents: From Biomolecules to Supramolecular Medicinal Chemistry.作为治疗剂的离子通道和转运体:从生物分子到超分子药物化学
Biomedicines. 2022 Apr 12;10(4):885. doi: 10.3390/biomedicines10040885.
3
Mechanistic Pathways and Molecular Targets of Plant-Derived Anticancer -Kaurane Diterpenes.

本文引用的文献

1
Cisplatin : an old drug with a newfound efficacy -- from mechanisms of action to cytotoxicity.顺铂:一种老药的新疗效——从作用机制到细胞毒性。
Expert Opin Pharmacother. 2013 Sep;14(13):1839-57. doi: 10.1517/14656566.2013.813934. Epub 2013 Jul 22.
2
In vitro biological activity of essential oils and isolated furanosesquiterpenes from the neglected vegetable Smyrnium olusatrum L. (Apiaceae).被忽视蔬菜 Smyrnium olusatrum L.(伞形科)精油和分离得到的呋喃倍半萜的体外生物活性。
Food Chem. 2013 Jun 1;138(2-3):808-13. doi: 10.1016/j.foodchem.2012.11.075. Epub 2012 Nov 27.
3
Global burden of cancer in 2008: a systematic analysis of disability-adjusted life-years in 12 world regions.
植物源抗癌-贝壳杉烷二萜的作用机制途径和分子靶点。
Biomolecules. 2020 Jan 16;10(1):144. doi: 10.3390/biom10010144.
4
A halogen bond-mediated highly active artificial chloride channel with high anticancer activity.一种具有高抗癌活性的卤素键介导的高活性人工氯离子通道。
Chem Sci. 2018 Mar 15;9(17):4044-4051. doi: 10.1039/c8sc00602d. eCollection 2018 May 7.
5
Volatile secondary metabolites as aposematic olfactory signals and defensive weapons in aquatic environments.挥发性次生代谢物作为水生环境中的警戒性嗅觉信号和防御武器。
Proc Natl Acad Sci U S A. 2017 Mar 28;114(13):3451-3456. doi: 10.1073/pnas.1614655114. Epub 2017 Mar 13.
6
Sensing marine biomolecules: smell, taste, and the evolutionary transition from aquatic to terrestrial life.感知海洋生物分子:嗅觉、味觉以及从水生到陆生生活的进化转变。
Front Chem. 2014 Oct 16;2:92. doi: 10.3389/fchem.2014.00092. eCollection 2014.
2008 年全球癌症负担:12 个世界区域按失能调整生命年衡量的系统分析。
Lancet. 2012 Nov 24;380(9856):1840-50. doi: 10.1016/S0140-6736(12)60919-2. Epub 2012 Oct 16.
4
A forgotten vegetable (Smyrnium olusatrum L., Apiaceae) as a rich source of isofuranodiene.一种被遗忘的蔬菜(水芹,伞形科)是异呋喃并二烯的丰富来源。
Food Chem. 2012 Dec 15;135(4):2852-62. doi: 10.1016/j.foodchem.2012.07.027. Epub 2012 Jul 16.
5
Natural products as sources of new drugs over the 30 years from 1981 to 2010.天然产物:1981 年至 2010 年 30 年间的新药来源。
J Nat Prod. 2012 Mar 23;75(3):311-35. doi: 10.1021/np200906s. Epub 2012 Feb 8.
6
Innovative functional cAMP assay for studying G protein-coupled receptors: application to the pharmacological characterization of GPR17.创新的功能性 cAMP 检测法用于研究 G 蛋白偶联受体:在 GPR17 的药理学特征研究中的应用。
Purinergic Signal. 2011 Dec;7(4):463-8. doi: 10.1007/s11302-011-9245-8. Epub 2011 Jul 20.
7
Development of natural anti-tumor drugs by microorganisms.微生物天然抗肿瘤药物的开发。
J Biosci Bioeng. 2011 May;111(5):501-11. doi: 10.1016/j.jbiosc.2010.12.026. Epub 2011 Jan 28.
8
Synthesis and biological evaluation of 2-alkynyl-N6-methyl-5'-N-methylcarboxamidoadenosine derivatives as potent and highly selective agonists for the human adenosine A3 receptor.2-炔基-N6-甲基-5'-N-甲基甲酰胺基腺苷衍生物作为人腺苷A3受体强效且高选择性激动剂的合成与生物学评价
J Med Chem. 2009 Dec 10;52(23):7897-900. doi: 10.1021/jm900754g.
9
Anticancer drug discovery in the future: an evolutionary perspective.未来的抗癌药物发现:进化视角。
Drug Discov Today. 2009 Dec;14(23-24):1136-42. doi: 10.1016/j.drudis.2009.09.006. Epub 2009 Oct 1.
10
Impact of natural products on developing new anti-cancer agents.天然产物对新型抗癌药物研发的影响。
Chem Rev. 2009 Jul;109(7):3012-43. doi: 10.1021/cr900019j.