• 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

海洋纤毛虫中分离得到的 Euplotin C 的抗癌活性及其对人黑色素瘤细胞的作用。

Anticancer Activity of Euplotin C, Isolated from the Marine Ciliate , Against Human Melanoma Cells.

机构信息

Department of Pharmacy, University of Pisa, via Bonanno 6, 56126 Pisa, Italy.

Department of Biotechnology, Chemistry and Pharmacy, University of Siena, Via Aldo Moro 2, 53100 Siena, Italy.

出版信息

Mar Drugs. 2018 May 16;16(5):166. doi: 10.3390/md16050166.

DOI:10.3390/md16050166
PMID:29772645
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5983297/
Abstract

Cutaneous melanoma is the most serious type of skin cancer, so new cytotoxic weapons against novel targets in melanoma are of great interest. Euplotin C (EC), a cytotoxic secondary metabolite of the marine ciliate , was evaluated in the present study on human cutaneous melanoma cells to explore its anti-melanoma activity and to gain more insight into its mechanism of action. EC exerted a marked cytotoxic effect against three different human melanoma cell lines (A375, 501Mel and MeWo) with a potency about 30-fold higher than that observed in non-cancer cells (HDFa cells). A pro-apoptotic activity and a decrease in melanoma cell migration by EC were also observed. At the molecular level, the inhibition of the Erk and Akt pathways, which control many aspects of melanoma aggressiveness, was shown. EC cytotoxicity was antagonized by dantrolene, a ryanodine receptor (RyR) antagonist, in a concentration-dependent manner. A role of RyR as a direct target of EC was also suggested by molecular modelling studies. In conclusion, our data provide the first evidence of the anti-melanoma activity of EC, suggesting it may be a promising new scaffold for the development of selective activators of RyR to be used for the treatment of melanoma and other cancer types.

摘要

皮肤黑色素瘤是最严重的皮肤癌类型,因此针对黑色素瘤新型靶点的新型细胞毒性药物具有重要意义。Euplotin C(EC)是一种海洋纤毛虫的细胞毒性次级代谢产物,本研究评估了其对人皮肤黑色素瘤细胞的抗黑色素瘤活性,并深入研究了其作用机制。EC 对三种不同的人黑色素瘤细胞系(A375、501Mel 和 MeWo)具有明显的细胞毒性作用,其效力比非癌细胞(HDFa 细胞)高约 30 倍。EC 还观察到促凋亡活性和黑色素瘤细胞迁移减少。在分子水平上,显示了抑制控制黑色素瘤侵袭性的许多方面的 Erk 和 Akt 通路。丹曲林钠(一种肌浆网钙释放通道(RyR)拮抗剂)以浓度依赖的方式拮抗 EC 的细胞毒性。分子建模研究还提示 RyR 是 EC 的直接作用靶点。总之,我们的数据首次提供了 EC 抗黑色素瘤活性的证据,表明它可能是一种有前途的新型骨架,可用于开发选择性 RyR 激活剂,用于治疗黑色素瘤和其他癌症类型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304c/5983297/af30fda9d4a1/marinedrugs-16-00166-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304c/5983297/6a7df84ead37/marinedrugs-16-00166-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304c/5983297/7da81d457ebf/marinedrugs-16-00166-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304c/5983297/64e9e15249e3/marinedrugs-16-00166-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304c/5983297/990360970623/marinedrugs-16-00166-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304c/5983297/af30fda9d4a1/marinedrugs-16-00166-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304c/5983297/6a7df84ead37/marinedrugs-16-00166-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304c/5983297/7da81d457ebf/marinedrugs-16-00166-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304c/5983297/64e9e15249e3/marinedrugs-16-00166-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304c/5983297/990360970623/marinedrugs-16-00166-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/304c/5983297/af30fda9d4a1/marinedrugs-16-00166-g005.jpg

相似文献

1
Anticancer Activity of Euplotin C, Isolated from the Marine Ciliate , Against Human Melanoma Cells.海洋纤毛虫中分离得到的 Euplotin C 的抗癌活性及其对人黑色素瘤细胞的作用。
Mar Drugs. 2018 May 16;16(5):166. doi: 10.3390/md16050166.
2
Cytotoxic effects and apoptotic signalling mechanisms of the sesquiterpenoid euplotin C, a secondary metabolite of the marine ciliate Euplotes crassus, in tumour cells.海洋纤毛虫粗壮游仆虫的次生代谢产物倍半萜类化合物优波亭C在肿瘤细胞中的细胞毒性作用及凋亡信号传导机制
Apoptosis. 2006 May;11(5):829-43. doi: 10.1007/s10495-006-5700-3.
3
The secondary metabolite euplotin C induces apoptosis-like death in the marine ciliated protist Euplotes vannus.次生代谢产物真核生物素C可诱导海洋纤毛原生生物 vannus 中出现类似凋亡的死亡。
J Eukaryot Microbiol. 2009 May-Jun;56(3):263-9. doi: 10.1111/j.1550-7408.2009.00396.x.
4
Antimicrobial activity of euplotin C, the sesquiterpene taxonomic marker from the marine ciliate Euplotes crassus.海洋纤毛虫粗壮游仆虫的倍半萜分类学标志物真核菌素C的抗菌活性。
Antimicrob Agents Chemother. 2004 Oct;48(10):3828-33. doi: 10.1128/AAC.48.10.3828-3833.2004.
5
Action mechanisms of the secondary metabolite euplotin C: signaling and functional role in Euplotes.次生代谢产物真核素C的作用机制:在游仆虫中的信号传导及功能作用
J Eukaryot Microbiol. 2008 Sep-Oct;55(5):365-73. doi: 10.1111/j.1550-7408.2008.00335.x.
6
Molecular mechanisms of euplotin C-induced apoptosis: involvement of mitochondrial dysfunction, oxidative stress and proteases.优洛托品C诱导细胞凋亡的分子机制:线粒体功能障碍、氧化应激和蛋白酶的作用
Apoptosis. 2007 Aug;12(8):1349-63. doi: 10.1007/s10495-007-0075-7.
7
Identification and molecular characterization of cytochrome P450 (CYP450) family genes in the marine ciliate Euplotes crassus: The effect of benzo[a]pyrene and beta-naphthoflavone.海洋纤毛虫厚岸真核生物中细胞色素P450(CYP450)家族基因的鉴定与分子特征:苯并[a]芘和β-萘黄酮的影响
Comp Biochem Physiol C Toxicol Pharmacol. 2017 Jun;196:71-80. doi: 10.1016/j.cbpc.2017.03.012. Epub 2017 Mar 21.
8
Biophysical effects of the natural product euplotin C on the Paramecium membrane.天然产物依普菌素 C 对草履虫膜的生物物理效应。
J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2009 Nov;195(11):1061-9. doi: 10.1007/s00359-009-0479-7. Epub 2009 Sep 24.
9
Pro-Apoptotic Activity of the Marine Sponge Metabolites Pelorol and 5--Ilimaquinone on Human 501Mel Melanoma Cells.海洋海绵代谢产物 Pelorol 和 5--Ilimaquinone 对人 501Mel 黑素瘤细胞的促凋亡活性。
Mar Drugs. 2022 Jun 28;20(7):427. doi: 10.3390/md20070427.
10
Oxyfadichalcone C inhibits melanoma A375 cell proliferation and metastasis via suppressing PI3K/Akt and MAPK/ERK pathways.氧杂二芳基查尔酮 C 通过抑制 PI3K/Akt 和 MAPK/ERK 通路抑制黑素瘤 A375 细胞增殖和转移。
Life Sci. 2018 Aug 1;206:35-44. doi: 10.1016/j.lfs.2018.05.032. Epub 2018 May 18.

引用本文的文献

1
Tanshinone IIA and Cryptotanshinone Counteract Inflammation by Regulating Gene and miRNA Expression in Human SGBS Adipocytes.丹参酮 IIA 和隐丹参酮通过调节人 SGBS 脂肪细胞中的基因和 miRNA 表达来对抗炎症。
Biomolecules. 2023 Jun 23;13(7):1029. doi: 10.3390/biom13071029.
2
Complexing the Marine Sesquiterpene Euplotin C by Means of Cyclodextrin-Based Nanosponges: A Preliminary Investigation.通过基于环糊精的纳米海绵络合海洋倍半萜类化合物 Euplotin C:初步研究。
Mar Drugs. 2022 Oct 29;20(11):682. doi: 10.3390/md20110682.
3
Marine Compounds for Melanoma Treatment and Prevention.

本文引用的文献

1
Overcoming resistance to targeted therapy with immunotherapy and combination therapy for metastatic melanoma.采用免疫疗法和联合疗法克服转移性黑色素瘤对靶向治疗的耐药性。
Oncotarget. 2017 Jun 16;8(43):75675-75686. doi: 10.18632/oncotarget.18523. eCollection 2017 Sep 26.
2
Biological Function of MicroRNA193a-3p in Health and Disease.微小RNA193a - 3p在健康与疾病中的生物学功能
Int J Genomics. 2017;2017:5913195. doi: 10.1155/2017/5913195. Epub 2017 Sep 5.
3
New perspectives for targeting RAF kinase in human cancer.针对人类癌症中 RAF 激酶的新视角。
海洋化合物在黑色素瘤治疗和预防中的应用。
Int J Mol Sci. 2022 Sep 7;23(18):10284. doi: 10.3390/ijms231810284.
4
Pro-Apoptotic Activity of the Marine Sponge Metabolites Pelorol and 5--Ilimaquinone on Human 501Mel Melanoma Cells.海洋海绵代谢产物 Pelorol 和 5--Ilimaquinone 对人 501Mel 黑素瘤细胞的促凋亡活性。
Mar Drugs. 2022 Jun 28;20(7):427. doi: 10.3390/md20070427.
5
Bioactive molecules from ciliates: Structure, activity, and applicative potential.纤毛虫来源的生物活性分子:结构、活性及应用潜力。
J Eukaryot Microbiol. 2022 Sep;69(5):e12887. doi: 10.1111/jeu.12887. Epub 2022 Jan 28.
6
Tailoring of silica-based nanoporous pod by spermidine multi-activity.通过多胺的多种活性对硅基纳米多孔豆荚进行剪裁。
Sci Rep. 2020 Dec 3;10(1):21142. doi: 10.1038/s41598-020-77957-4.
7
miRNA Modulation and Antitumor Activity by the Extra-Virgin Olive Oil Polyphenol Oleacein in Human Melanoma Cells.特级初榨橄榄油多酚橄榄苦苷对人黑色素瘤细胞的miRNA调节及抗肿瘤活性
Front Pharmacol. 2020 Sep 23;11:574317. doi: 10.3389/fphar.2020.574317. eCollection 2020.
8
Alternative Options for Skin Cancer Therapy via Regulation of AKT and Related Signaling Pathways.通过调节 AKT 及相关信号通路实现皮肤癌治疗的替代方案。
Int J Mol Sci. 2020 Sep 18;21(18):6869. doi: 10.3390/ijms21186869.
9
Tumor Suppressor Role of hsa-miR-193a-3p and -5p in Cutaneous Melanoma.hsa-miR-193a-3p 和 -5p 在皮肤黑色素瘤中的抑瘤作用。
Int J Mol Sci. 2020 Aug 27;21(17):6183. doi: 10.3390/ijms21176183.
10
Hydroxytyrosol Modulates Adipocyte Gene and miRNA Expression Under Inflammatory Condition.羟基酪醇在炎症条件下调节脂肪细胞基因和 miRNA 表达。
Nutrients. 2019 Oct 17;11(10):2493. doi: 10.3390/nu11102493.
Nat Rev Cancer. 2017 Nov;17(11):676-691. doi: 10.1038/nrc.2017.79. Epub 2017 Oct 6.
4
RSF1 functions as an oncogene in osteosarcoma and is regulated by XIST/miR-193a-3p axis.RSF1 在骨肉瘤中作为癌基因发挥作用,并受 XIST/miR-193a-3p 轴调控。
Biomed Pharmacother. 2017 Nov;95:207-214. doi: 10.1016/j.biopha.2017.08.068. Epub 2017 Sep 12.
5
Epidemiological trends in skin cancer.皮肤癌的流行病学趋势
Dermatol Pract Concept. 2017 Apr 30;7(2):1-6. doi: 10.5826/dpc.0702a01. eCollection 2017 Apr.
6
Identification of plasma microRNAs as new potential biomarkers with high diagnostic power in human cutaneous melanoma.鉴定血浆微小RNA作为人类皮肤黑色素瘤具有高诊断效能的新型潜在生物标志物。
Tumour Biol. 2017 May;39(5):1010428317701646. doi: 10.1177/1010428317701646.
7
Targeted agents and immunotherapies: optimizing outcomes in melanoma.靶向药物和免疫疗法:优化黑色素瘤的治疗效果。
Nat Rev Clin Oncol. 2017 Aug;14(8):463-482. doi: 10.1038/nrclinonc.2017.43. Epub 2017 Apr 4.
8
Tumor-promoting effects of cannabinoid receptor type 1 in human melanoma cells.1型大麻素受体在人黑色素瘤细胞中的促肿瘤作用。
Toxicol In Vitro. 2017 Apr;40:272-279. doi: 10.1016/j.tiv.2017.01.018. Epub 2017 Jan 26.
9
Drug Affinity Responsive Target Stability (DARTS) Identifies Laurifolioside as a New Clathrin Heavy Chain Modulator.药物亲和力响应靶点稳定性(DARTS)鉴定出月桂叶苷是一种新的网格蛋白重链调节剂。
J Nat Prod. 2016 Oct 28;79(10):2681-2692. doi: 10.1021/acs.jnatprod.6b00627. Epub 2016 Oct 5.
10
Structural Basis for Gating and Activation of RyR1.兰尼碱受体1(RyR1)门控与激活的结构基础
Cell. 2016 Sep 22;167(1):145-157.e17. doi: 10.1016/j.cell.2016.08.075.