Cell cycle kinetic effects of tamoxifen on human breast cancer cells. Flow cytometric analyses of DNA content, BrdU labeling, Ki-67, PCNA, and statin expression

Ann N Y Acad Sci. 1993 Nov 30:698:174-81. doi: 10.1111/j.1749-6632.1993.tb17206.x.

Abstract

Tamoxifen is known to inhibit the growth of some human mammary carcinoma cells; this effect is accompanied by a decrease in the proportion of cells synthesizing DNA. In this work, flow cytometry of DNA and of bromodeoxyuridine labeling and the evaluation of the cell cycle-related antigens Ki-67, PCNA, and statin were used to investigate the changes in the proliferation kinetics of MCF-7 cells before and after treatment with 10(-7) M TAM. The treatment with TAM induced a significant decrease in the fraction of S-phase cells and an increase in those with a DNA content typical of G0/1 phase. The TAM-induced block in G0/1 is paralleled by a decrease in the frequency of cells expressing Ki-67 and PCNA, and by an increase in statin-positive (G0) cells. These results confirmed that the TAM-induced inhibition of cell growth is associated with major changes in the cell cycle parameters of MCF-7 cells, and provide the first experimental evidence that two main mechanisms are operating: the accumulation of cells in G1, before the onset of S-phase, and the exit of some cells from the cycling compartment.

Publication types

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

MeSH terms

  • Biomarkers, Tumor / analysis*
  • Breast Neoplasms / pathology*
  • Bromodeoxyuridine
  • Cell Cycle / drug effects*
  • Cell Cycle Proteins
  • Cell Line
  • DNA, Neoplasm / analysis
  • DNA, Neoplasm / metabolism*
  • Female
  • Flow Cytometry / methods
  • Fluorescent Antibody Technique
  • Humans
  • Immunohistochemistry / methods
  • Ki-67 Antigen
  • Kinetics
  • Neoplasm Proteins / analysis*
  • Neoplasm Proteins / biosynthesis
  • Nuclear Proteins / analysis*
  • Nuclear Proteins / biosynthesis
  • Peptide Elongation Factor 1
  • Proliferating Cell Nuclear Antigen
  • Protein Biosynthesis
  • Proteins / analysis*
  • Tamoxifen / toxicity*
  • Tumor Cells, Cultured

Substances

  • Biomarkers, Tumor
  • Cell Cycle Proteins
  • DNA, Neoplasm
  • EEF1A2 protein, human
  • Ki-67 Antigen
  • Neoplasm Proteins
  • Nuclear Proteins
  • Peptide Elongation Factor 1
  • Proliferating Cell Nuclear Antigen
  • Proteins
  • Tamoxifen
  • Bromodeoxyuridine