Literature DB >> 29023715

A new parameter of growth inhibition for cell proliferation assays.

Francesco P Fiorentino1,2, Luigi Bagella2,3, Irene Marchesi1.   

Abstract

Cell proliferation assays are performed by four decades to test the anti-proliferative activity of natural products and synthetic compounds in cell cultures. In cancer research, they are widely employed to evaluate drug efficacy in in vitro tumor models, such as established cell lines, primary cultures, and recently developed three-dimensional tumor organoids. In this manuscript, we demonstrated that current employed parameters used by researchers to quantify in vitro growth inhibition, IC50 and GI50 , lead to a misinterpretation of results based on the exponential, and not linear, proliferation of the cells in culture. Therefore, we introduce a new parameter for the analysis of growth inhibition in cell proliferation assays, termed relative population doubling capacity, that can be employed to properly quantify the anti-proliferative activity of tested compounds and to compare drug efficacy between distinct cell models.
© 2017 Wiley Periodicals, Inc.

Entities:  

Keywords:  cell proliferation; cell viability; cytotoxicity; drug screening; drug toxicity

Mesh:

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Year:  2017        PMID: 29023715     DOI: 10.1002/jcp.26208

Source DB:  PubMed          Journal:  J Cell Physiol        ISSN: 0021-9541            Impact factor:   6.384


  2 in total

1.  The live cell DNA stain SiR-Hoechst induces DNA damage responses and impairs cell cycle progression.

Authors:  Onur Sen; Adrian T Saurin; Jonathan M G Higgins
Journal:  Sci Rep       Date:  2018-05-21       Impact factor: 4.379

2.  Bromodomain Inhibitor JQ1 Provides Novel Insights and Perspectives in Rhabdomyosarcoma Treatment.

Authors:  Irene Marchesi; Milena Fais; Francesco Paolo Fiorentino; Valentina Bordoni; Luca Sanna; Stefano Zoroddu; Luigi Bagella
Journal:  Int J Mol Sci       Date:  2022-03-25       Impact factor: 5.923

  2 in total

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