Syrian hamster embryo cell transformation assay at pH 7.0

Topic: Carcinogenicity

Test Method Number:
TM2005-03 (EU)
Short Name of TM:
SHE 7.0 CTA
Year received:
2005
Responsible Organisation:
Protocol(s)/SOP(s):
136

Method Description

The in vitro CTA using Syrian hamster embryonic (SHE) cells at pH 7.0 is aimed at detecting the carcinogenic potential of chemicals. The assay is based on the change of the phenotypic features of cells undergoing the first steps of the conversion from normal cells to neoplastic-like cell foci with oncogenic properties. Carcinogenesis is a complex multistage process by which normal cells are transformed into cancer cells characterised by an accumulation of changes at the cellular, genetic and epigenetic level. In vitro CTAs such as the SHE CTA have been shown to recapitulate a multistage process that closely models some stages of in vivo carcinogenesis. A minimum of four phenotypic stages appears to be involved in cell transformation. These include (from primary to fully malignant cells):

  1. a block in cellular differentiation,
  2. acquisition of immortality, characterised by unlimited lifespan, an aneuploidy karyotype and a decreased...

The in vitro CTA using Syrian hamster embryonic (SHE) cells at pH 7.0 is aimed at detecting the carcinogenic potential of chemicals. The assay is based on the change of the phenotypic features of cells undergoing the first steps of the conversion from normal cells to neoplastic-like cell foci with oncogenic properties. Carcinogenesis is a complex multistage process by which normal cells are transformed into cancer cells characterised by an accumulation of changes at the cellular, genetic and epigenetic level. In vitro CTAs such as the SHE CTA have been shown to recapitulate a multistage process that closely models some stages of in vivo carcinogenesis. A minimum of four phenotypic stages appears to be involved in cell transformation. These include (from primary to fully malignant cells):

  1. a block in cellular differentiation,
  2. acquisition of immortality, characterised by unlimited lifespan, an aneuploidy karyotype and a decreased genetic stability;
  3. acquisition of tumorigenicity, which is closely associated with the in vitro phenotypes of foci formation, anchorage independent growth in semi-solid agar and autocrine growth factor production;
  4. full malignancy, including metastasis when the cells are injected into a suitable host, supporting the biological relevance of in vitro transformation to in vivo carcinogenicity.

The assay is based on the change of the phenotypic features of cell colonies undergoing the first steps of the conversion from normal cells to neoplastic-like cells with oncogenic properties

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