• 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

天然法尼基转移酶抑制剂在癌症治疗中的应用概述。

An overview on natural farnesyltransferase inhibitors for efficient cancer therapy.

机构信息

School of Life Science, Ludong University, Yantai, Shandong, China.

出版信息

J Enzyme Inhib Med Chem. 2020 Dec;35(1):1027-1044. doi: 10.1080/14756366.2020.1732366.

DOI:10.1080/14756366.2020.1732366
PMID:32308053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7191900/
Abstract

As one of the world's five terminally ills, tumours can cause important genetic dysfunction. However, some current medicines for tumours usually have strong toxic side effects and are prone to drug resistance. Studies have found that farnesyltransferase inhibitors (FTIs) extracted from natural materials have a good inhibiting ability on tumours with fewer side effects. This article describes several FTIs extracted from natural materials and clarifies the current research progress, which provides a new choice for the treatment of tumours.

摘要

作为世界五大绝症之一,肿瘤会导致重要的遗传功能障碍。然而,目前一些治疗肿瘤的药物通常具有较强的毒副作用,并且容易产生耐药性。研究发现,从天然物质中提取的法呢基转移酶抑制剂(FTIs)对肿瘤具有良好的抑制作用,副作用较少。本文介绍了几种从天然物质中提取的 FTIs,并阐明了当前的研究进展,为肿瘤的治疗提供了新的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/916f704bbb3e/IENZ_A_1732366_F0009_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/6ae74d924a4d/IENZ_A_1732366_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/fc83b21b0040/IENZ_A_1732366_F0002_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/2dd3ab631699/IENZ_A_1732366_F0003_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/d8ff7d7fa8c3/IENZ_A_1732366_F0004_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/3ee4aa8a113d/IENZ_A_1732366_F0005_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/0fb1cd095a01/IENZ_A_1732366_F0006_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/a7480b77ffe3/IENZ_A_1732366_F0007_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/304bfb937c60/IENZ_A_1732366_F0008_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/916f704bbb3e/IENZ_A_1732366_F0009_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/6ae74d924a4d/IENZ_A_1732366_F0001_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/fc83b21b0040/IENZ_A_1732366_F0002_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/2dd3ab631699/IENZ_A_1732366_F0003_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/d8ff7d7fa8c3/IENZ_A_1732366_F0004_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/3ee4aa8a113d/IENZ_A_1732366_F0005_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/0fb1cd095a01/IENZ_A_1732366_F0006_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/a7480b77ffe3/IENZ_A_1732366_F0007_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/304bfb937c60/IENZ_A_1732366_F0008_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be10/7191900/916f704bbb3e/IENZ_A_1732366_F0009_B.jpg

相似文献

1
An overview on natural farnesyltransferase inhibitors for efficient cancer therapy.天然法尼基转移酶抑制剂在癌症治疗中的应用概述。
J Enzyme Inhib Med Chem. 2020 Dec;35(1):1027-1044. doi: 10.1080/14756366.2020.1732366.
2
Farnesyltransferase inhibitors: a comprehensive review based on quantitative structural analysis.法尼基转移酶抑制剂:基于定量结构分析的综合评价。
Curr Med Chem. 2013;20(38):4888-923. doi: 10.2174/09298673113206660262.
3
Inhibition of farnesyltransferase: a rational approach to treat cancer?
J Enzyme Inhib Med Chem. 2007 Apr;22(2):127-40. doi: 10.1080/14756360601072841.
4
Implications of farnesyltransferase and its inhibitors as a promising strategy for cancer therapy.法尼基转移酶及其抑制剂作为癌症治疗有希望策略的意义。
Semin Cancer Biol. 2019 Jun;56:128-134. doi: 10.1016/j.semcancer.2017.10.010. Epub 2017 Oct 31.
5
Farnesyltransferase and geranylgeranyltransferase I inhibitors and cancer therapy: lessons from mechanism and bench-to-bedside translational studies.法尼基转移酶和香叶基香叶基转移酶I抑制剂与癌症治疗:来自作用机制及从 bench 到 bedside 的转化研究的经验教训
Oncogene. 2000 Dec 27;19(56):6584-93. doi: 10.1038/sj.onc.1204146.
6
Recent advances in understanding the antineoplastic mechanisms of farnesyltransferase inhibitors.法尼基转移酶抑制剂抗肿瘤机制研究的最新进展
Cancer Res. 2005 Oct 15;65(20):9109-12. doi: 10.1158/0008-5472.CAN-05-2635.
7
Farnesyltransferase inhibitors: where are we now?法尼基转移酶抑制剂:我们现在在哪里?
Expert Opin Investig Drugs. 2010 Dec;19(12):1569-80. doi: 10.1517/13543784.2010.535516. Epub 2010 Nov 18.
8
Ras homologue enriched in brain is a critical target of farnesyltransferase inhibitors in non-small cell lung cancer cells.脑富集 Ras 同源物是法尼基转移酶抑制剂在非小细胞肺癌细胞中的关键靶标。
Cancer Lett. 2010 Nov 1;297(1):117-25. doi: 10.1016/j.canlet.2010.05.004.
9
Lipid posttranslational modifications. Farnesyl transferase inhibitors.脂质翻译后修饰。法尼基转移酶抑制剂。
J Lipid Res. 2006 Jan;47(1):15-31. doi: 10.1194/jlr.R500012-JLR200. Epub 2005 Nov 8.
10
Phenothiazine-based CaaX competitive inhibitors of human farnesyltransferase bearing a cysteine, methionine, serine or valine moiety as a new family of antitumoral compounds.基于吩噻嗪的人法尼基转移酶的CaaX竞争性抑制剂,带有半胱氨酸、甲硫氨酸、丝氨酸或缬氨酸部分,作为一类新的抗肿瘤化合物。
Bioorg Med Chem Lett. 2015 Oct 15;25(20):4447-52. doi: 10.1016/j.bmcl.2015.09.008. Epub 2015 Sep 7.

引用本文的文献

1
Utilizing , a Significant Veterinary Pathogen, in Lung Cancer Treatment: A Novel Approach.利用一种重要的兽医病原体进行肺癌治疗:一种新方法。
Arch Razi Inst. 2025 Feb 1;80(1):1-10. doi: 10.32592/ARI.2025.80.1.1. eCollection 2025 Feb.
2
Farnesyltransferase inhibitor lonafarnib suppresses respiratory syncytial virus infection by blocking conformational change of fusion glycoprotein.法尼基转移酶抑制剂 lonafarnib 通过阻断融合糖蛋白构象改变来抑制呼吸道合胞病毒感染。
Signal Transduct Target Ther. 2024 Jun 10;9(1):144. doi: 10.1038/s41392-024-01858-5.
3
Clinical research progress of callisperes of drug-loaded microsphere arterial chemoembolisation in the treatment of solid tumors.

本文引用的文献

1
Evaluation of antileishmanial activity of harzialactone a isolated from the marine-derived fungus sp.对从海洋来源真菌中分离得到的哈齐内酯A的抗利什曼原虫活性的评估
Nat Prod Res. 2021 May;35(10):1644-1647. doi: 10.1080/14786419.2019.1619725. Epub 2019 May 29.
2
Larvicidal, Histopathological, Antibacterial Activity of Indigenous Fungus sp. Against L and (Say) (Diptera: Culicidae) and Its Acetylcholinesterase Inhibition and Toxicity Assessment of Zebrafish ().本土真菌对致倦库蚊(双翅目:蚊科)的杀幼虫、组织病理学、抗菌活性及其对斑马鱼的乙酰胆碱酯酶抑制作用和毒性评估
Front Microbiol. 2019 Mar 18;10:427. doi: 10.3389/fmicb.2019.00427. eCollection 2019.
3
载药微球动脉化疗栓塞术治疗实体瘤的临床研究进展
Discov Oncol. 2024 May 13;15(1):161. doi: 10.1007/s12672-024-01030-z.
4
New Perspectives in Treating Acute Myeloid Leukemia: Driving towards a Patient-Tailored Strategy.治疗急性髓系白血病的新视角:朝着个体化治疗策略迈进。
Int J Mol Sci. 2022 Mar 31;23(7):3887. doi: 10.3390/ijms23073887.
5
Essential Oil Inhibits Hepatocellular Carcinoma Metastasis via Suppression of DEPDC1 Dependent Wnt/β-Catenin Signaling Pathway.精油通过抑制DEPDC1依赖的Wnt/β-连环蛋白信号通路抑制肝细胞癌转移。
Front Cell Dev Biol. 2021 Jun 29;9:664791. doi: 10.3389/fcell.2021.664791. eCollection 2021.
6
Structure, catalysis, and inhibition mechanism of prenyltransferase. prenyltransferase 的结构、催化和抑制机制。
IUBMB Life. 2021 Jan;73(1):40-63. doi: 10.1002/iub.2418. Epub 2020 Nov 27.
7
Natural Products Attenuating Biosynthesis, Processing, and Activity of Ras Oncoproteins: State of the Art and Future Perspectives.天然产物对 Ras 癌蛋白生物合成、加工和活性的抑制作用:现状与未来展望。
Biomolecules. 2020 Nov 10;10(11):1535. doi: 10.3390/biom10111535.
Immunomodulatory effects of a mycelium extract of Cordyceps (Paecilomyces hepiali; CBG-CS-2): a randomized and double-blind clinical trial.
蛹草拟青霉(Paecilomyces hepiali;CBG-CS-2)菌丝体提取物的免疫调节作用:一项随机双盲临床试验。
BMC Complement Altern Med. 2019 Mar 29;19(1):77. doi: 10.1186/s12906-019-2483-y.
4
Ergosterol peroxide from marine fungus Phoma sp. induces ROS-dependent apoptosis and autophagy in human lung adenocarcinoma cells.海洋真菌 Phoma sp. 中的麦角甾醇过氧化物诱导人肺腺癌细胞中 ROS 依赖的细胞凋亡和自噬。
Sci Rep. 2018 Dec 18;8(1):17956. doi: 10.1038/s41598-018-36411-2.
5
The biological evaluation of fusidic acid and its hydrogenation derivative as antimicrobial and anti-inflammatory agents.夫西地酸及其氢化衍生物作为抗菌和抗炎剂的生物学评价。
Infect Drug Resist. 2018 Oct 24;11:1945-1957. doi: 10.2147/IDR.S176390. eCollection 2018.
6
Pharmacological activities of antroquinonol- Mini review.安石榴醌的药理学活性- 小型综述。
Chem Biol Interact. 2019 Jan 5;297:8-15. doi: 10.1016/j.cbi.2018.10.009. Epub 2018 Oct 19.
7
Antibacterial activity and in situ efficacy of Bidens pilosa Linn and Dichrostachys cinerea Wight et Arn extracts against common diarrhoea-causing waterborne bacteria.鬼针草和芒萁提取物对常见腹泻性水源性细菌的抗菌活性及体内疗效。
BMC Complement Altern Med. 2018 Jun 1;18(1):171. doi: 10.1186/s12906-018-2230-9.
8
Synthesis and In Vitro Evaluation of the Ras Farnesyltransferase Inhibitor Pepticinnamin E.Ras法尼基转移酶抑制剂Pepticinnamin E的合成与体外评价
Angew Chem Int Ed Engl. 1998 May 18;37(9):1236-1239. doi: 10.1002/(SICI)1521-3773(19980518)37:9<1236::AID-ANIE1236>3.0.CO;2-F.
9
Construction of a mutant of Actinoplanes sp. N902-109 that produces a new rapamycin analog.放线菌 N902-109 突变株的构建及其产生新型雷帕霉素类似物。
Chin J Nat Med. 2018 Mar;16(3):210-218. doi: 10.1016/S1875-5364(18)30049-9.
10
(teak) - A review on its phytochemical and therapeutic potential.柚木(teak)——植物化学及治疗潜能的综述。
Nat Prod Res. 2019 Aug;33(16):2338-2354. doi: 10.1080/14786419.2018.1440217. Epub 2018 Mar 6.