Anti-c-myc DNA increases differentiation and decreases colony formation by HL-60 cells |
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Authors: | Erica L Wickstrom Thomas A Bacon Audrey Gonzalez Gary H Lyman Eric Wikstrom |
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Institution: | (1) Department of Chemistry, University of South Florida, 33620 Tampa, Florida;(2) Department of Internal Medicine, University of South Florida, 33620 Tampa, Florida;(3) Department of Biochemistry and Molecular Biology, University of South Florida, 33620 Tampa, Florida;(4) Present address: Center for Cancer Research, Department of Biology, Massachusetts Institute of Technology, 02139 Cambridge, MA |
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Abstract: | Summary The proto-oncogene c-myc, whose gene product has a role in replication, is overexpressed in the human promyelocytic leukemia HL-60 cell line. Treatment
of HL-60 cells with an antisense oligodeoxyribonucleotide complementary to the start codon and the next four codons of c-myc mRNA has previously been observed to inhibit c-myc protein expression and cell proliferation in a sequence-specific, dose-dependent manner. Comparable effects are seen upon
treatment of HL-60 cells with dimethylsulfoxide (Me2SO), which is also know to induce granulocytic differentiation of HL-60 cells. Hence, the effects of antisense oligomers on
cellular differentiation were examine and compared with Me2SO. Differentiation of HL-60 cells into forms with granulocytic characteristics was found to be enhanced in a sequence-specific
manner by the anti-c-myc oligomer. No synergism was observed between the anti-c-myc oligomer and Me2SO in stimulating cellular differentiation. In contrast, synergism did appear in the inhibition of cell proliferation. Finally,
the anti-c-myc oligomer uniformly inhibited colony formation in semisolid medium. It is possible that further reduction in the level of
c-myc expression by antisense oligomer inhibition may be sufficient to allow terminal granulocytic differentiation and reverse
transformation.
This work was supported by grants to E. W. from the National Institutes of Health, Bethesda, MD (CA 42960), and the Leukemia
Society of America. |
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Keywords: | oligodeoxynucleotides hybrid arrest proliferation granulocytes dimethylsulfoxide |
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