Literature DB >> 3698942

Statistical analyses for in vitro cytogenetic assays using Chinese hamster ovary cells.

B H Margolin, M A Resnick, J Y Rimpo, P Archer, S M Galloway, A D Bloom, E Zeiger.   

Abstract

It is a widely held view that objective statistical criteria are needed for the evaluation of genetic toxicity assays. This paper presents statistical methods for the analysis of data from in vitro sister chromatid exchange (SCE) and chromosome aberration tests that use Chinese hamster ovary cells. For SCEs, an extensive study of solvent control results demonstrated that there is a substantial interday component of variability in the data, and that a Poisson sampling model is applicable to data generated via the protocol of Galloway et al [1985]. Consequently, a trend test for evidence of a dose response is proposed for such SCE data. As an illustration of this statistical method, analysis of data previously considered to be negative [Gulati et al, 1985] indicates that di(2-ethyl-hexyl) phthalate induces a weak, but reproducible, SCE dose response in CHO cells. Monte Carlo methods are used to show that the trend test is more sensitive than four other statistical procedures considered for the analysis of Poisson-distributed SCEs. A similar trend test for dose response in proportions is proposed for chromosome aberration data, where the percent of cells with chromosome aberrations is the response of interest. Sensitivity (or power) studies indicate that three doses and a control with 50 cells/dose point is a reasonable design for an in vitro SCE study that uses the Galloway et al protocol. For in vitro chromosome aberrations, however, three doses and a control with 100 cells/dose point appears to produce too insensitive an assay; an increase to 200 cells/dose point in the Galloway et al protocol seems worthy of serious consideration.

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Year:  1986        PMID: 3698942     DOI: 10.1002/em.2860080203

Source DB:  PubMed          Journal:  Environ Mutagen        ISSN: 0192-2521


  9 in total

1.  Chromosomal aberrations induced by cobaltous chloride in mice in vivo.

Authors:  S Palit; A Sharma; G Talukder
Journal:  Biol Trace Elem Res       Date:  1991-05       Impact factor: 3.738

2.  Comparison of clastogenic effects of antimony and bismuth as trioxides on mice in vivo.

Authors:  N Gurnani; A Sharma; G Talukder
Journal:  Biol Trace Elem Res       Date:  1993 May-Jun       Impact factor: 3.738

3.  Cytotoxicity of zinc chloride in mice in vivo.

Authors:  T Gupta; G Talukder; A Sharma
Journal:  Biol Trace Elem Res       Date:  1991-08       Impact factor: 3.738

4.  Clastogenic activity of strontium chloride on bone marrow cells in vivo.

Authors:  S Ghosh; G Talukder; A Sharma
Journal:  Biol Trace Elem Res       Date:  1990-04       Impact factor: 3.738

5.  Interaction between two group IV metals--lead and zirconium--in bone marrow cells of Mus musculus in vivo.

Authors:  H Dhir; S Ghosh; A Sharma; G Talukder
Journal:  Biometals       Date:  1992       Impact factor: 2.949

6.  Modifying effect of iron on lead-induced clastogenicity in mouse bone marrow cells.

Authors:  H Dhir; A Sharma; G Talukder
Journal:  Biol Trace Elem Res       Date:  1992-09       Impact factor: 3.738

7.  Comparison of the clastogenic effects of antimony trioxide on mice in vivo following acute and chronic exposure.

Authors:  N Gurnani; A Sharma; G Talukder
Journal:  Biometals       Date:  1992       Impact factor: 2.949

8.  A comparative study of the aneugenic and polyploidy-inducing effects of fisetin and two model Aurora kinase inhibitors.

Authors:  P Gollapudi; L S Hasegawa; D A Eastmond
Journal:  Mutat Res Genet Toxicol Environ Mutagen       Date:  2014-03-26       Impact factor: 2.873

Review 9.  Genetic toxicology: current status of methods of carcinogen identification.

Authors:  R W Tennant; E Zeiger
Journal:  Environ Health Perspect       Date:  1993-04       Impact factor: 9.031

  9 in total

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