In vitro genotoxicity test approaches with better predictivity: Summary of an IWGT workshop. - Anses - Agence nationale de sécurité sanitaire de l’alimentation, de l’environnement et du travail Access content directly
Journal Articles Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis Year : 2011

In vitro genotoxicity test approaches with better predictivity: Summary of an IWGT workshop.

Stefan Pfuhler
  • Function : Author
Mick Fellows
  • Function : Author
Jan van Benthem
  • Function : Author
Raffaella Corvi
  • Function : Author
Rodger Curren
  • Function : Author
Kerry Dearfield
  • Function : Author
Paul Fowler
  • Function : Author
Roland Frötschl
  • Function : Author
Azeddine Elhajouji
  • Function : Author
Ludovic Le Hégarat
Toshio Kasamatsu
  • Function : Author
Hajime Kojima
  • Function : Author
Gladys Ouédraogo
  • Function : Author
Andrew Scott
  • Function : Author


Improving current in vitro genotoxicity tests is an ongoing task for genetic toxicologists. Further, the question on how to deal with positive in vitro results that are demonstrated to not predict genotoxicity or carcinogenicity potential in rodents or humans is a challenge. These two aspects were addressed at the 5th International Workshop on Genotoxicity Testing (IWGT) held in Basel, Switzerland, on August 17-19, 2009. The objectives of the working group (WG) were to make recommendations on the use of cell types or lines, if possible, and to provide evaluations of promising new approaches. Results obtained in rodent cell lines with impaired p53 function (L5178Y, V79, CHL and CHO cells) and human p53-competent cells (peripheral blood lymphocytes, TK6 and HepG2 cells) suggest that a reduction in the percentage of non-relevant positive results for carcinogenicity prediction can be achieved by careful selection of cells used without decreasing the sensitivity of the assays. Therefore, the WG suggested using p53- competent - preferably human - cells in in vitro micronucleus or chromosomal aberration tests. The use of the hepatoma cell line HepaRG for genotoxicity testing was considered promising since these cells possess better phase I and II metabolizing potential compared to cell lines commonly used in this area and may overcome the need for the addition of S9. For dermally applied compounds, the WG agreed that in vitro reconstructed skin models, once validated, will be useful to follow up on positive results from standard in vitro assays as they resemble the properties of human skin (barrier function, metabolism). While the reconstructed skin micronucleus assay has been shown to be further advanced, there was also consensus that the Comet assay should be further evaluated due to its independence from cell proliferation and coverage of a wider spectrum of DNA damage.



Dates and versions

hal-00595074 , version 1 (23-05-2011)



Stefan Pfuhler, Mick Fellows, Jan van Benthem, Raffaella Corvi, Rodger Curren, et al.. In vitro genotoxicity test approaches with better predictivity: Summary of an IWGT workshop.. Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 2011, 723 (2), pp.101-107. ⟨10.1016/j.mrgentox.2011.03.013⟩. ⟨hal-00595074⟩


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