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Effect of neplanocin A on differentiation, nucleic acid methylation, and c-myc mRNA expression in human promyelocytic leukemia cells.

Abstract
The effect of the cyclopentenyl adenosine analog neplanocin A (NPC) on cell growth and differentiation was examined in the human promyelocytic leukemia cell line HL-60. Continuous exposure of HL-60 cells to 0.1-3.3 microM NPC resulted in a progressive reduction in cell growth which was accompanied by an increase in differentiation to cells with a myelocyte and neutrophil morphology. The latter effect was expressed as an increase in the capacity of cells to reduce nitro blue tetrazolium and reached a level of 40% of the total cell population. Preceding the phenotypic changes was the preferential inhibition of RNA and DNA methylation in comparison to inhibition of their synthesis which coincided with the formation of a metabolite of NPC with the chromatographic characteristics of S-adenosyl-L-methionine (AdoMet). In addition, c-myc mRNA expression, which is amplified in HL-60 cells, was markedly reduced following NPC treatment. These results indicate that NPC is an effective inhibitor of RNA and DNA methylation resulting from its conversion to an analog of AdoMet, and that these effects appear to be responsible for reduced c-myc RNA expression and the induction of myeloid differentiation in this cell line.
AuthorsJ Linevsky, M B Cohen, K D Hartman, M C Knode, R I Glazer
JournalMolecular pharmacology (Mol Pharmacol) Vol. 28 Issue 1 Pg. 45-50 (Jul 1985) ISSN: 0026-895X [Print] United States
PMID3860729 (Publication Type: Journal Article)
Chemical References
  • Antimetabolites, Antineoplastic
  • DNA, Neoplasm
  • RNA, Neoplasm
  • neplanocin A
  • Adenosine
Topics
  • Adenosine (analogs & derivatives, metabolism, pharmacology)
  • Antimetabolites, Antineoplastic
  • Cell Differentiation (drug effects)
  • Cell Division (drug effects)
  • Cell Line
  • DNA, Neoplasm (genetics)
  • Gene Expression Regulation (drug effects)
  • Humans
  • Leukemia, Myeloid, Acute (genetics, pathology)
  • Methylation
  • Oncogenes
  • RNA, Neoplasm (genetics)

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