A continuum of transformed phenotypes in C3H/10T1/2 derivatives
- 1 January 1988
- journal article
- research article
- Published by Oxford University Press (OUP) in Carcinogenesis: Integrative Cancer Research
- Vol. 9 (9) , 1695-1700
- https://doi.org/10.1093/carcin/9.9.1695
Abstract
Two-stage transformants have been isolated from C3H/10T1/2 cells exposed to UV-irradiation followed by treatment with TPA. These UV-TDTx cells form foci in co-culture with C3H/10T1/2 cells only in the presence of TPA. In the absence of TPA, UV-TDTx cells are indistinguishable from control C3H/10T1/2 cells in co-cultures. Single-step transformants of C3H/10T1/2 cells isolated after exposure to high doses of chemical carcinogens, however, show TPA-independent focus formation in co-culture with C3H/10T1/2 cells. We now show that three independently isolated two-stage UV + TPA transformants as well as a single-step, high dose methylcholanthrene (MCA) transformant (MCATxle) isolated in our laboratory are anchorage-dependent and non-tumorigenic. In contrast, another single-step, high dose MCA transformant (MCACI#16/39) known to contain an activated c-Ki-ras gene shows TPA-independent focus formation in mixed culture with C3H/10T1/2 cells, anchorage independence and tumorigenicity. Analysis of UV-TDTx:C3H/10T1/2 and MCACI#16/39:C3H/10T1/2 somatic cell hybrids indicates that a similar percentage of hybrids of each cell type are able to form foci in co-culture with C3H/10T1/2 cells. However, focus-forming UV-TDTx:C3H/10T1/2 hybrids remain dependent on TPA for focus formation in mixed culture.This publication has 11 references indexed in Scilit:
- Modulation of transforming growth factor type beta action by activated ras and c-myc.Molecular and Cellular Biology, 1987
- Colony size, cell density and nature of the tumor promoter are critical variables in expression of a transformed phenotype (focus formation) in co-cultures of UV-TDTx and C3H10T1/2 cellsCarcinogenesis: Integrative Cancer Research, 1987
- Ultraviolet Irradiation Transforms C3H10T1/2 Cells to a Unique, Suppressible PhenotypeScience, 1986
- ENHANCED EXPRESSION OF C-MYC AND DECREASED EXPRESSION OF C-FOS PROTOONCOGENES IN CHEMICALLY AND RADIATION-TRANSFORMED C3H-10T1/2 CL 8 MOUSE EMBRYO CELL-LINES1986
- Mechanism of activation of a human oncogeneNature, 1982
- Relationship between x-ray exposure and malignant transformation in C3H 10T1/2 cells.Proceedings of the National Academy of Sciences, 1980
- Passage of phenotypes of chemically transformed cells via transfection of DNA and chromatin.Proceedings of the National Academy of Sciences, 1979
- Chemical carcinogens produce mutations to ouabain resistance in transformable C3H/10T1/2 Cl 8 mouse fibroblasts.Proceedings of the National Academy of Sciences, 1979
- TRANSFORMATION OF MOUSE C3H-10T1-2 CELLS BY SINGLE AND FRACTIONATED DOSES OF X-RAYS AND FISSION-SPECTRUM NEUTRONS1979
- 2-STAGE CHEMICAL ONCOGENESIS IN CULTURES OF C3H-10T1-2 CELLS1976