Morphological transformation of C3H/10T1/2 CL8 cells by procarcinogens
✍ Scribed by Oshiro, Y. ;Balwierz, P. S.
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1982
- Weight
- 218 KB
- Volume
- 4
- Category
- Article
- ISSN
- 0192-2521
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
In order to increase the sensitivity of the C3H/10T1/2 CL8 (10T1/2) cell transformation system, we increased the chemical exposure period to a total of 6 days (two consecutive 3‐day exposures). Using this modified procedure, we transformed 10T1/2 cells with procarcinogens such as aflatoxin B~1~, benz(a)anthracene, and 4‐nitroquinoline‐1‐oxide which have been negative in the standard 10T1/2 cell transformation assay. However, β‐naphthylamine was inconclusive and 2‐acetylamino‐fluorine was negative in this modified assay system. Our results demonstrate that a simple modification of the 10T1/2 cell transformation method can increase the sensitivity to some procarcinogens that require metabolic activation.
📜 SIMILAR VOLUMES
The C3WlOTf CLS(1OTi) cell transformation assay has been used as an important in vitro tool for screening potential carcinogens. In this paper we describe an experimental design that increases the sensitivity and specificity of the assay. One half of the total dishes was allocated to the solvent con
## Abstract The uptake of ^3^H‐thymidine in post‐confluent cultures of methylcholanthrene‐transformed C3H/10T1/2 mouse embryo cells was markedly higher than in their non‐transformed counterparts. In a reconstruction experiment as few as 2% transformed cells could be detected by increased thymidine
Malignant transformation of mouse fibroblasts was produced by electroporation with restriction enzymes. Similar transformation frequencies were observed with Pstl, Pvull, and Xbal, which cut genomic DNA at similar overall frequencies but have different termini, i.e., a 3' overhang, a blunt end, and