• 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

抗癌药物的细胞药理学研究:EORTC-PAMM 小组的建议。

Cellular pharmacology studies of anticancer agents: recommendations from the EORTC-PAMM group.

机构信息

Molecular Pharmacology Unit, Department of Applied research and Technological Development, Fondazione IRCCS Istituto Nazionale dei Tumori, Via Amadeo 42, 20133, Milan, Italy.

Institut für Pharmazeutische und Medizinische Chemie, -Klinische Pharmazie, Westfälische Wilhelms-Universität Münster, 48149, Münster, Germany.

出版信息

Cancer Chemother Pharmacol. 2018 Mar;81(3):427-441. doi: 10.1007/s00280-017-3502-7. Epub 2017 Dec 28.

DOI:10.1007/s00280-017-3502-7
PMID:29285635
Abstract

An increasing number of manuscripts focus on the in vitro evaluation of established and novel anti-tumor agents in experimental models. Whilst the design of such in vitro assays is inherently flexible, some of these studies lack the minimum information necessary to critically evaluate their relevance or have been carried out under unsuitable conditions. The use of appropriate and robust methods and experimental design has important implications for generating results that are reliable, relevant, and reproducible. The Pharmacology and Molecular Mechanisms (PAMM) group of the European Organization for Research and Treatment of Cancer (EORTC) is the largest group of academic scientists working on drug development and bundle decades of expertise in this field. This position paper addresses all researchers with an interest in the preclinical and cellular pharmacology of anti-tumor agents and aims at generating basic recommendations for the correct use of compounds to be tested for anti-tumor activity using a range of preclinical cellular models of cancer.

摘要

越来越多的论文侧重于在实验模型中对已建立和新型抗肿瘤药物进行体外评估。虽然此类体外检测的设计具有内在的灵活性,但其中一些研究缺乏批判性评估其相关性所需的最低信息,或者是在不合适的条件下进行的。使用适当和稳健的方法和实验设计对于生成可靠、相关和可重复的结果具有重要意义。欧洲癌症研究与治疗组织(EORTC)的药理学和分子机制(PAMM)小组是从事药物开发的最大的学术科学家团体,拥有数十年在该领域的专业知识。本立场文件面向所有对抗肿瘤药物的临床前和细胞药理学感兴趣的研究人员,旨在为使用一系列临床前癌症细胞模型测试抗肿瘤活性的化合物的正确使用生成基本建议。

相似文献

1
Cellular pharmacology studies of anticancer agents: recommendations from the EORTC-PAMM group.抗癌药物的细胞药理学研究:EORTC-PAMM 小组的建议。
Cancer Chemother Pharmacol. 2018 Mar;81(3):427-441. doi: 10.1007/s00280-017-3502-7. Epub 2017 Dec 28.
2
Pharmacologically directed strategies in academic anticancer drug discovery based on the European NCI compounds initiative.基于欧洲国家癌症研究所化合物计划的学术性抗癌药物研发中的药理学导向策略。
Br J Cancer. 2017 Jul 11;117(2):195-202. doi: 10.1038/bjc.2017.167. Epub 2017 Jun 13.
3
A Brief Guide to Performing Pharmacological Studies : Reflections from the EORTC-PAMM Course "Preclinical and Early-phase Clinical Pharmacology".执行药理学研究的简要指南:来自 EORTC-PAMM 课程“临床前和早期临床药理学”的反思。
Anticancer Res. 2019 Jul;39(7):3413-3418. doi: 10.21873/anticanres.13485.
4
In vitro assays and techniques utilized in anticancer drug discovery.在抗癌药物发现中使用的体外检测和技术。
J Appl Toxicol. 2019 Jan;39(1):38-71. doi: 10.1002/jat.3658. Epub 2018 Aug 2.
5
Chemoresistance of Cancer Cells: Requirements of Tumor Microenvironment-mimicking Models in Anti-Cancer Drug Development.癌细胞的化学抗性:在抗癌药物开发中模拟肿瘤微环境模型的要求。
Theranostics. 2018 Oct 22;8(19):5259-5275. doi: 10.7150/thno.29098. eCollection 2018.
6
[Preclinical data as basis for the design of clinical studies].[临床研究设计的基础——临床前数据]
Onkologie. 2008;31 Suppl 2:34-8. doi: 10.1159/000113449. Epub 2008 Apr 18.
7
Current mathematical models for cancer drug discovery.当前用于癌症药物发现的数学模型。
Expert Opin Drug Discov. 2017 Aug;12(8):785-799. doi: 10.1080/17460441.2017.1340271. Epub 2017 Jun 22.
8
Gold compounds as anticancer agents: chemistry, cellular pharmacology, and preclinical studies.金化合物作为抗癌剂:化学、细胞药理学和临床前研究。
Med Res Rev. 2010 May;30(3):550-80. doi: 10.1002/med.20168.
9
Contemporary pre-clinical development of anticancer agents--what are the optimal preclinical models?当代抗癌药物的临床前开发——什么样的临床前模型是最佳的?
Eur J Cancer. 2009 Nov;45(16):2768-81. doi: 10.1016/j.ejca.2009.08.008. Epub 2009 Sep 15.
10
Novel anticancer agents and targets: recent advances and future perspectives.新型抗癌药物和靶点:最新进展与未来展望。
Mini Rev Med Chem. 2013 Jul;13(9):1239-55. doi: 10.2174/13895575113139990061.

引用本文的文献

1
Targeting pan-essential pathways in cancer with cytotoxic chemotherapy: challenges and opportunities.用细胞毒化疗靶向癌症的普遍必需途径:挑战与机遇。
Cancer Chemother Pharmacol. 2023 Oct;92(4):241-251. doi: 10.1007/s00280-023-04562-3. Epub 2023 Jul 15.
2
The deubiquitinase USP8 regulates ovarian cancer cell response to cisplatin by suppressing apoptosis.去泛素化酶USP8通过抑制细胞凋亡来调节卵巢癌细胞对顺铂的反应。
Front Cell Dev Biol. 2022 Dec 12;10:1055067. doi: 10.3389/fcell.2022.1055067. eCollection 2022.
3
3D Cancer Models: Depicting Cellular Crosstalk within the Tumour Microenvironment.
3D癌症模型:描绘肿瘤微环境中的细胞间相互作用
Cancers (Basel). 2021 Sep 14;13(18):4610. doi: 10.3390/cancers13184610.
4
Characterizing the reproducibility in using a liver microphysiological system for assaying drug toxicity, metabolism, and accumulation.描述使用肝微生理系统测定药物毒性、代谢和积累的可重复性。
Clin Transl Sci. 2021 May;14(3):1049-1061. doi: 10.1111/cts.12969. Epub 2021 Apr 3.
5
Exposure time versus cytotoxicity for anticancer agents.暴露时间与抗癌药物的细胞毒性。
Cancer Chemother Pharmacol. 2019 Aug;84(2):359-371. doi: 10.1007/s00280-019-03863-w. Epub 2019 May 17.
6
Aurantoside C Targets and Induces Apoptosis in Triple Negative Breast Cancer Cells.橙皮苷 C 靶向并诱导三阴性乳腺癌细胞凋亡。
Mar Drugs. 2018 Oct 1;16(10):361. doi: 10.3390/md16100361.