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Enhancement of Methotrexate Resistance and Dihydrofolate Reductase Gene Amplification by Treatment of Mouse 3T6 Cells with Hydroxyurea

Overview
Journal Mol Cell Biol
Specialty Cell Biology
Date 1983 Jun 1
PMID 6877240
Citations 67
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Abstract

We investigated various parameters associated with the initial selection of mouse 3T6 cells for resistance to single concentrations of methotrexate and characterized resistant colonies for the presence of additional (amplified) copies of the dihydrofolate reductase gene. Our results indicate that the frequency of occurrence of dihydrofolate reductase gene amplification varies with the selecting concentration of methotrexate and is highly variable between clonally derived sublines of mouse 3T6 cells. Second, we increased the frequency of occurrence of cells with amplified dihydrofolate reductase genes by transiently inhibiting DNA synthesis with hydroxyurea before the selection of cells in single concentrations of methotrexate. This effect was dependent on the concentration of hydroxyurea, the time of exposure to the drug, and the time interval between the removal of hydroxyurea and the selection of cells in methotrexate.

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References
1.
Woodcock D, Cooper I . Evidence for double replication of chromosomal DNA segments as a general consequence of DNA replication inhibition. Cancer Res. 1981; 41(6):2483-90. View

2.
Fischer G . Nutritional and amethopterin-resistant characteristics of leukemic clones. Cancer Res. 1959; 19(4):372-6. View

3.
Hamrell M, Laszlo J, Sedwick W . Transient induction of phenotypic resistance in human lymphoblastoid cells following sequential use of two antifolates. Mol Pharmacol. 1981; 19(3):491-5. View

4.
Wahl G, Padgett R, Stark G . Gene amplification causes overproduction of the first three enzymes of UMP synthesis in N-(phosphonacetyl)-L-aspartate-resistant hamster cells. J Biol Chem. 1979; 254(17):8679-89. View

5.
Skoog L, Nordenskjold B . Effects of hydroxyurea and 1-beta-D-arabinofuranosyl-cytosine on deoxyribonucleotide pools in mouse embryo cells. Eur J Biochem. 1971; 19(1):81-9. DOI: 10.1111/j.1432-1033.1971.tb01290.x. View