Is there an accumulation of cells during G2 in some acute lymphoblastic leukaemias?

Cell Tissue Kinet. 1990 Jul;23(4):251-60. doi: 10.1111/j.1365-2184.1990.tb01122.x.

Abstract

In some cases of acute lymphoblastic leukaemia (ALL) the percentage of cells in G2 + M is higher than anticipated when compared with the percentage in S phase. This increase in G2 + M, as detected by flow cytometry measurement of DNA content, may be due to an accumulation of cells, either in G2 or during the end of S phase; it may also be related to the existence of small tetraploid clones generally ignored by cytogeneticists. In order to identify possible subpopulations of cells with a DNA index greater than or equal to 2.0, we have compared the results of a cytogenetic analysis to the G2 + M values. We have also studied the distribution of S phase cells in 24 cases of ALL by incorporating 5-bromodeoxyuridine, labelling the cells by indirect immunofluorescence, and analysing them by flow cytometry after propidium iodide staining. The distribution of cells during S phase was quantified: no accumulation of cells was ever observed at the end of S phase. The question of the existence of small tetraploid clones, G2 arrested cells or cells with a G2 elongation remains open. However, we feel that it is more probable that, in this pathology, an elongation of the duration of G2 occurs.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Bone Marrow / pathology*
  • Bone Marrow / ultrastructure
  • Bromodeoxyuridine
  • Cell Count
  • Child
  • Child, Preschool
  • DNA, Neoplasm / analysis*
  • Female
  • Flow Cytometry
  • Humans
  • Infant
  • Interphase*
  • Karyotyping
  • Lymphocytes / pathology
  • Male
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma / pathology*
  • Propidium
  • Staining and Labeling

Substances

  • DNA, Neoplasm
  • Propidium
  • Bromodeoxyuridine