Published July 18, 2019 | Version v.1

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

  • 1. Fondazione Pisana per la Scienza-ONLUS, Pisa, Italy
  • 2. Molecular Pharmacology Unit, Department of Applied Research and Technological
  • 3. Amsterdam UMC, VU University of Amsterdam, Medical Oncology, Cancer Center Amsterdam, Amsterdam, the Netherlands
  • 4. Amsterdam UMC, VU University of Amsterdam, Medical Oncology, Cancer Center Amsterdam, Amsterdam, the Netherlands; Department of Biological, Chemical and Pharmaceutical Sciences and Technologies (STEBICEF), University of Palermo, Palermo, Italy
  • 5. Laboratory of Pharmacology, Department of Experimental Oncology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia manics@ncrc.ac.rs.

Description

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 issue 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 preclinical drug-discovery phases and target validation.

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31262863 (PMID)
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