Partial reversion of the transformed phenotype in HRAS-transfected tumorigenic cells by transfer of a human gene
Journal Article
·
· Proc. Natl. Acad. Sci. U.S.A.; (United States)
The transformed phenotype of rat FE-8 cells transfected by an activated human HRAS gene was suppressed upon fusion with normal cells. An experimental approach was developed to identify and isolate a human gene capable of suppressing the transforming activity of the HRAS oncogene in FE-8 cells. Genomic DNA from human placenta was introduced into FE-8 cells by cotransfection with the plasmid pY3 conferring hygromycin B resistance. Transfectants were selected in medium containing hygromycin B. HRAS-transformed FE-8 cells showed an increased sensitivity toward ouabain when compared to their normal counterparts. Therefore, the population of transfected hygromycin B-resistant cells was treated with ouabain to eliminate cells with a transformed phenotype. Ouabain selection resulted in a small number of cell clones exhibiting a more normal phenotype. The clones had lost the morphology of transformed cells and required anchorage for growth. The tumorigenicity of transfectants in nude mice was reduced by not completely abolished. FE-8 revertants continued to express the p21 RAS protein. Human repetitive sequences contained in the DNA of a secondary transfectant were used for isolation of the suppressor gene from reverted FE-8 cells. The cloned DNA fragment was transfected into tumorigenic FE-8 cells and conferred a partial reversion of the transformed phenotype.
- Research Organization:
- Ludwig Institute for Cancer Research, Bern (Switzerland)
- OSTI ID:
- 6658885
- Journal Information:
- Proc. Natl. Acad. Sci. U.S.A.; (United States), Journal Name: Proc. Natl. Acad. Sci. U.S.A.; (United States) Vol. 85:5; ISSN PNASA
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
550401* -- Genetics-- Tracer Techniques
59 BASIC BIOLOGICAL SCIENCES
ANIMAL CELLS
ANIMALS
CARBOHYDRATES
CARDIAC GLYCOSIDES
CARDIOTONICS
CARDIOVASCULAR AGENTS
DRUGS
FETAL MEMBRANES
GENE RECOMBINATION
GENE REGULATION
GENE REPRESSORS
GENES
GLYCOSIDES
INHIBITION
MAMMALS
MEMBRANES
MOLECULAR BIOLOGY
MORPHOLOGICAL CHANGES
NUCLEOPROTEINS
ONCOGENES
ORGANIC COMPOUNDS
OUABAIN
PHENOTYPE
PLACENTA
PROTEINS
RATS
RODENTS
STROPHANTHINS
TUMOR CELLS
VERTEBRATES
59 BASIC BIOLOGICAL SCIENCES
ANIMAL CELLS
ANIMALS
CARBOHYDRATES
CARDIAC GLYCOSIDES
CARDIOTONICS
CARDIOVASCULAR AGENTS
DRUGS
FETAL MEMBRANES
GENE RECOMBINATION
GENE REGULATION
GENE REPRESSORS
GENES
GLYCOSIDES
INHIBITION
MAMMALS
MEMBRANES
MOLECULAR BIOLOGY
MORPHOLOGICAL CHANGES
NUCLEOPROTEINS
ONCOGENES
ORGANIC COMPOUNDS
OUABAIN
PHENOTYPE
PLACENTA
PROTEINS
RATS
RODENTS
STROPHANTHINS
TUMOR CELLS
VERTEBRATES