Literature DB >> 22951948

Comparative analysis of eight cytotoxicity assays evaluated within the ACuteTox Project.

R Clothier1, M J Gómez-Lechón, A Kinsner-Ovaskainen, A Kopp-Schneider, J E O'Connor, P Prieto, S Stanzel.   

Abstract

A comparative analysis of eight cytotoxicity assays [the 3T3 and normal human keratinocytes Neutral Red Uptake (NRU) assay, the primary rat hepatocytes, human HepG2 and 3T3 MTT assay, and the human A.704, SH-SY5Y and HepG2 cells propidium iodide (PI) assay] included in several work packages of the EU Integrated Project ACuteTox, has been carried out. The aim was to evaluate whether cells originating from liver, kidney and brain provided different in vitro acute toxicity results, and the influence of primary liver cells versus cell lines originated from the same tissue. Spearman rank correlation analysis and Hierarchical Cluster Analysis were performed based on the IC50 (50% inhibitory concentrations for the endpoint measured) values generated for 57 chemicals. A relatively large number of neurotoxicants and hepatotoxicants were included which allowed to examine the impact of chemicals with specific tissue toxicity on the results. Our analyses confirmed the similarity between the NRU assays and between the two hepatic cell systems related MTT assays. The type of assay appears to have the greatest influence upon the clustering result regardless of the origin of the cells used. The information provided by the NRU and MTT assays differed from that provided by the PI assay. This approach did not allow to show tissue specific toxicity but it does reveal the effectiveness of the clustering methodology for choosing assays for a testing program for predicting e.g. acute oral toxicity in humans.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22951948     DOI: 10.1016/j.tiv.2012.08.015

Source DB:  PubMed          Journal:  Toxicol In Vitro        ISSN: 0887-2333            Impact factor:   3.500


  7 in total

1.  Optimal experimental designs for dose-response studies with continuous endpoints.

Authors:  Tim Holland-Letz; Annette Kopp-Schneider
Journal:  Arch Toxicol       Date:  2014-08-26       Impact factor: 5.153

2.  LUCS (Light-Up Cell System), a universal high throughput assay for homeostasis evaluation in live cells.

Authors:  Sylvain Derick; Camille Gironde; Pierre Perio; Karine Reybier; Françoise Nepveu; Alain Jauneau; Christophe Furger
Journal:  Sci Rep       Date:  2017-12-22       Impact factor: 4.379

3.  Nonanimal Models for Acute Toxicity Evaluations: Applying Data-Driven Profiling and Read-Across.

Authors:  Daniel P Russo; Judy Strickland; Agnes L Karmaus; Wenyi Wang; Sunil Shende; Thomas Hartung; Lauren M Aleksunes; Hao Zhu
Journal:  Environ Health Perspect       Date:  2019-04       Impact factor: 9.031

4.  Cytotoxicity and Mitochondrial Effects of Phenolic and Quinone-Based Mitochondria-Targeted and Untargeted Antioxidants on Human Neuronal and Hepatic Cell Lines: A Comparative Analysis.

Authors:  Carlos Fernandes; Afonso J C Videira; Caroline D Veloso; Sofia Benfeito; Pedro Soares; João D Martins; Beatriz Gonçalves; José F S Duarte; António M S Santos; Paulo J Oliveira; Fernanda Borges; José Teixeira; Filomena S G Silva
Journal:  Biomolecules       Date:  2021-10-29

5.  Suitability of Human Mesenchymal Stem Cells Derived from Fetal Umbilical Cord (Wharton's Jelly) as an Alternative In Vitro Model for Acute Drug Toxicity Screening.

Authors:  Ioannis Christodoulou; Maria Goulielmaki; Andreas Kritikos; Panagiotis Zoumpourlis; Georgios Koliakos; Vassilis Zoumpourlis
Journal:  Cells       Date:  2022-03-24       Impact factor: 6.600

Review 6.  Big data in chemical toxicity research: the use of high-throughput screening assays to identify potential toxicants.

Authors:  Hao Zhu; Jun Zhang; Marlene T Kim; Abena Boison; Alexander Sedykh; Kimberlee Moran
Journal:  Chem Res Toxicol       Date:  2014-09-16       Impact factor: 3.739

7.  Use of LUCS (Light-Up Cell System) as an alternative live cell method to predict human acute oral toxicity.

Authors:  C Gironde; C Dufour; C Furger
Journal:  Toxicol Rep       Date:  2020-02-19
  7 in total

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