TY - JOUR
T1 - The carcinoGENOMICS project: critical selection of model compounds for the development of omics-based in vitro carcinogenicity screening assays.
AU - Vinken, M.
AU - Doktorova, T.
AU - Ellinger Ziegelbauer, H.
AU - Ahr, H.J.
AU - Lock, E.
AU - Carmichael, P.
AU - Roggen, E.
AU - van Delft, J.
AU - Kleinjans, J.
AU - Castell, J.
AU - Bort, R.
AU - Donato, T.
AU - Ryan, M.
AU - Corvi, R.
AU - Keun, H.
AU - Ebbels, T.
AU - Athersuch, T.
AU - Sansone, S.A.
AU - Rocca Serra, P.
AU - Stierum, R.
AU - Jennings, P.
AU - Pfaller, W.
AU - Gmuender, H.
AU - Vanhaecke, T.
AU - Rogiers, V.
PY - 2008/1/1
Y1 - 2008/1/1
N2 - Recent changes in the European legislation of chemical-related substances have forced the scientific community to speed up the search for alternative methods that could partly or fully replace animal experimentation. The Sixth Framework Program project carcinoGENOMICS was specifically raised to develop omics-based in vitro screens for testing the carcinogenic potential of chemical compounds in a pan-European context. This paper provides an in-depth analysis of the complexity of choosing suitable reference compounds used for creating and fine-tuning the in vitro carcinogenicity assays. First, a number of solid criteria for the selection of the model compounds are defined. Secondly, the strategy followed, including resources consulted, is described and the selected compounds are briefly illustrated. Finally, limitations and problems encountered during the selection procedure are discussed. Since selecting an appropriate set of chemicals is a frequent impediment in the early stages of similar research projects, the information provided in this paper might be extremely valuable
AB - Recent changes in the European legislation of chemical-related substances have forced the scientific community to speed up the search for alternative methods that could partly or fully replace animal experimentation. The Sixth Framework Program project carcinoGENOMICS was specifically raised to develop omics-based in vitro screens for testing the carcinogenic potential of chemical compounds in a pan-European context. This paper provides an in-depth analysis of the complexity of choosing suitable reference compounds used for creating and fine-tuning the in vitro carcinogenicity assays. First, a number of solid criteria for the selection of the model compounds are defined. Secondly, the strategy followed, including resources consulted, is described and the selected compounds are briefly illustrated. Finally, limitations and problems encountered during the selection procedure are discussed. Since selecting an appropriate set of chemicals is a frequent impediment in the early stages of similar research projects, the information provided in this paper might be extremely valuable
U2 - 10.1016/j.mrrev.2008.04.006
DO - 10.1016/j.mrrev.2008.04.006
M3 - Article
C2 - 18514569
SN - 1383-5742
VL - 659
SP - 202
EP - 210
JO - Mutation Research-Reviews in Mutation Research
JF - Mutation Research-Reviews in Mutation Research
IS - 3
ER -