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Recommended protocol for the Syrian hamster embryo (SHE) cell transformation assay
Authors:Maire Marie-Aline  Pant Kamala  Phrakonkham Pascal  Poth Albrecht  Schwind Karl-Rainer  Rast Claudine  Bruce Shannon Wilson  Sly Jamie E  Bohnenberger Susanne  Kunkelmann Thorsten  Schulz Markus  Vasseur Paule
Affiliation:Université Paul Verlaine de Metz, Metz, France. marie-aline.maire@univ-metz.fr
Abstract:The Syrian hamster embryo (SHE) cell transformation assay (CTA) is a short-term in vitro assay recommended as an alternative method for testing the carcinogenic potential of chemicals. SHE cells are "normal" cells since they are diploid, genetically stable, non-tumourigenic, and have metabolic capabilities for the activation of some classes of carcinogens. The CTA, first developed in the 1960s by Berwald and Sachs (1963,1964) [3,4], is based on the change of the phenotypic feature of cell colonies expressing the first steps of the conversion of normal to neoplastic-like cells with oncogenic properties. Pienta et al. (1977) [22] developed a protocol using cryopreserved cells to enhance practicality of the assay and limit sources of variability. Several variants of the assay are currently in use, which mainly differ by the pH at which the assay is performed. We present here the common version of the SHE pH 6.7 CTA and SHE pH 7.0 CTA protocols used in the ECVAM (European Centre for the Validation of Alternative Methods) prevalidation study on CTA reported in this issue. It is recommended that this protocol, in combination with the photo catalogues presented in this issue, should be used in the future and serve as a basis for the development of the OECD test guideline.
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