Glucocorticoid/oxysterol-induced DNA lysis in human leukemic cells

J Steroid Biochem Mol Biol. 1997 Apr;61(1-2):35-45. doi: 10.1016/s0960-0760(96)00256-7.

Abstract

Both glucocorticoids and oxysterols, steroids with quite different known transduction pathways, cause the death of lymphoid cells. Dual TUNEL/propidium iodide assays on sensitive human leukemic CEM-C7 clones treated with either steroid were clearly positive by 48 h, consistent with apoptosis. Both steroids evoked two distinctive types of DNA lysis: cleavage into large fragments of several different sizes and the classic "ladders", multiples of approximately 200 base pairs. Conventional gel electrophoresis showed that a small proportion of total DNA had undergone laddering 36-48 h after treatment with glucocorticoid or 24 h after oxysterol exposure. On field inversion gel electrophoresis of cellular DNA both steroids caused an increase in an array of large DNA fragments <50 kb in size. A 50 kb fragment appeared 36 h after treatment with either steroid, but only oxysterol treatment caused a significant increase in a 300 kb fragment. Oxysterol treatment did not result in DNA fragmentation in the resistant M10R5 subclone, which retained sensitivity to glucocorticoids. We conclude that glucocorticoids and oxysterols kill these cells with similar, but not identical, patterns of DNA lysis which occur just before or concomitant with the onset of cell death.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cell Division
  • DNA Fragmentation / drug effects*
  • DNA, Neoplasm / analysis
  • Dexamethasone / pharmacology*
  • Glucocorticoids / pharmacology*
  • Humans
  • Hydroxycholesterols / pharmacology*
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / pathology*
  • Tumor Cells, Cultured

Substances

  • DNA, Neoplasm
  • Glucocorticoids
  • Hydroxycholesterols
  • 25-hydroxycholesterol
  • Dexamethasone