Abstract |
Expression of the ras proto-oncogene mRNA in human myeloblastic leukemia (ML-1) cells was analyzed as a function of cDNA amplification by polymerase chain reaction (PCR). By using a pair of oligonucleotides that flank exon-2 from opposite strands (5' and 3') of H-ras cDNA for PCR amplification, ML-1 cells were found to express a 112 bp segment of the ras transcript. A rapid decline in the expression of this transcript was seen in cells treated with heptachlor, a chlorinated hydrocarbon insecticide. Expression of the same ras segment was not affected by treatment of ML-1 with the tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA). Furthermore, addition of serum to quiescent, heptachlor-treated cultures of ML-1 cells inhibited the effect of heptachlor and restored the expression of the ras protooncogene mRNA.
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Authors | L F Chuang, R Y Chuang |
Journal | Toxicology
(Toxicology)
Vol. 70
Issue 3
Pg. 283-92
( 1991)
ISSN: 0300-483X [Print] Ireland |
PMID | 1771636
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Actins
- Culture Media
- MAS1 protein, human
- Proto-Oncogene Mas
- RNA, Messenger
- Heptachlor
- Tetradecanoylphorbol Acetate
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Topics |
- Actins
(genetics)
- Base Sequence
- Blood
- Culture Media
- Gene Expression
(drug effects)
- Genes, ras
- Heptachlor
(pharmacology)
- Humans
- Leukemia, Myeloid, Acute
(genetics)
- Molecular Sequence Data
- Polymerase Chain Reaction
- Proto-Oncogene Mas
- RNA, Messenger
(genetics)
- Tetradecanoylphorbol Acetate
(pharmacology)
- Tumor Cells, Cultured
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