• 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

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。

A Brief Guide to Performing Pharmacological Studies : Reflections from the EORTC-PAMM Course "Preclinical and Early-phase Clinical Pharmacology".

机构信息

Fondazione Pisana per la Scienza-ONLUS, Pisa, Italy.

Molecular Pharmacology Unit, Department of Applied Research and Technological Development, Fondazione IRCCS, Istituto Nazionale dei Tumori, Milan, Italy.

出版信息

Anticancer Res. 2019 Jul;39(7):3413-3418. doi: 10.21873/anticanres.13485.

DOI:10.21873/anticanres.13485
PMID:31262863
Abstract

One aim of cell-based in vitro assays is to identify the best drug candidate to develop using the best tumor cell model. This is challenging in every anticancer drug discovery process. Briefly, we summarize the parameters to be taken into account when performing in vitro cell assays, in order to obtain reliable and reproducible results, which was fundamentally discussed by lecturers at the educational course on preclinical and early-phase clinical pharmacology studies, at the 40th Winter Meeting of the Pharmacology and Molecular Mechanisms Group of the European Organization for Research and Treatment of Cancer. Moreover, specific cellular sensitivity tests are described. In addition to monolayer in vitro cell models for the screening of new potential candidate drugs, three-dimensional tumor/cell tissue models are emerging as new pre-clinical tools that more closely reflect the in vivo microenvironment. Therefore, the use of different in vitro models for drug screening can enhance the predictability and reliability of pre-clinical drug-discovery phases and target validation.

摘要

基于细胞的体外检测的一个目的是确定最佳的候选药物,以便使用最佳的肿瘤细胞模型进行开发。在每个抗癌药物发现过程中,这都是具有挑战性的。简要地说,我们总结了在进行体外细胞检测时需要考虑的参数,以获得可靠和可重复的结果,这在欧洲癌症研究与治疗组织的药理学和分子机制小组第 40 届冬季会议上的临床前和早期临床药理学研究教育课程中,由讲师进行了基本讨论。此外,还描述了特定的细胞敏感性测试。除了用于筛选新的潜在候选药物的单层体外细胞模型外,三维肿瘤/细胞组织模型作为新的临床前工具正在出现,这些模型更能反映体内微环境。因此,使用不同的体外模型进行药物筛选可以提高临床前药物发现阶段和靶标验证的可预测性和可靠性。

相似文献

1
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.
2
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.
3
Is There Any Room for Pharmacometrics With Immuno-Oncology Drugs? Input from the EORTC-PAMM Course on Preclinical and Early-phase Clinical Pharmacology.免疫肿瘤药物的药物代谢动力学还有发展空间吗?来自 EORTC-PAMM 临床前和早期临床药理学课程的观点。
Anticancer Res. 2019 Jul;39(7):3419-3422. doi: 10.21873/anticanres.13486.
4
Functional human tissue assays.功能性人体组织检测
Drug Discov Today. 2007 May;12(9-10):382-8. doi: 10.1016/j.drudis.2007.03.012. Epub 2007 Apr 5.
5
To Combine or Not Combine: Drug Interactions and Tools for Their Analysis. Reflections from the EORTC-PAMM Course on Preclinical and Early-phase Clinical Pharmacology.是否合并:药物相互作用及其分析工具。从 EORTC-PAMM 临床前和早期临床药理学课程的反思。
Anticancer Res. 2019 Jul;39(7):3303-3309. doi: 10.21873/anticanres.13472.
6
Could 3D models of cancer enhance drug screening?癌症的3D模型能否增强药物筛选效果?
Biomaterials. 2020 Feb;232:119744. doi: 10.1016/j.biomaterials.2019.119744. Epub 2019 Dec 26.
7
[Responsibilities of clinical pharmacology in the early phase of drug development].[临床药理学在药物研发早期阶段的职责]
Med Klin (Munich). 2000 May;95(1 Spec No):31-40.
8
Anticancer Drug Development: The Way Forward.抗癌药物研发:前进之路
Oncologist. 1996;1(3):180-181.
9
[Clinical-pharmacological aspects to accelerate the development process from the preclinical to the clinical phase/1st communication: The contribution of clinical pharmacology].[加速从临床前到临床阶段开发进程的临床药理学方面/首次交流:临床药理学的贡献]
Arzneimittelforschung. 2004;54(5):251-8. doi: 10.1055/s-0031-1296967.
10
Miniaturized three-dimensional cancer model for drug evaluation.用于药物评估的小型化三维癌症模型。
Assay Drug Dev Technol. 2013 Sep;11(7):435-48. doi: 10.1089/adt.2012.483.

引用本文的文献

1
Drug screening and development cascade for Chagas disease: an update of in vitro and in vivo experimental models.用于恰加斯病的药物筛选和开发级联:体外和体内实验模型的最新进展。
Mem Inst Oswaldo Cruz. 2024 Jul 1;119:e240057. doi: 10.1590/0074-02760240057. eCollection 2024.
2
A review for cell-based screening methods in drug discovery.药物发现中基于细胞的筛选方法综述。
Biophys Rep. 2021 Dec 31;7(6):504-516. doi: 10.52601/bpr.2021.210042.
3
Cytotoxicity profiling of choline chloride-based natural deep eutectic solvents.基于氯化胆碱的天然低共熔溶剂的细胞毒性分析
RSC Adv. 2023 Jan 25;13(6):3520-3527. doi: 10.1039/d2ra07488e. eCollection 2023 Jan 24.
4
Enriching Chemical Space of Bioactive Scaffolds by New Ring Systems: Benzazocines and Their Metal Complexes as Potential Anticancer Drugs.通过新环系统丰富生物活性支架的化学空间:苯并氮杂卓及其金属配合物作为潜在的抗癌药物。
Inorg Chem. 2022 Dec 19;61(50):20445-20460. doi: 10.1021/acs.inorgchem.2c03134. Epub 2022 Dec 6.
5
Tumor Organoids as a Research Tool: How to Exploit Them.肿瘤类器官作为一种研究工具:如何利用它们。
Cells. 2022 Oct 31;11(21):3440. doi: 10.3390/cells11213440.
6
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.