Tectorigenin, an isoflavone of Pueraria thunbergiana Benth., induces differentiation and apoptosis in human promyelocytic leukemia HL-60 cells

Biol Pharm Bull. 2001 Oct;24(10):1117-21. doi: 10.1248/bpb.24.1117.

Abstract

Cytotoxic effects of six isoflavonoids, tectorigenin, glycitein, tectoridin, glycitin, 6''-O-xylosyltectoridin, and 6''-O-xylosylglycitin isolated from the flower of Pueraria thunbergiana Benth. together with genistein, a known differentiation and apoptosis inducer, were examined. Among these isoflavonoids, tectorigenin and genistein exhibited cytotoxicity against various human cancer cells; glycitein showed only mild cytotoxicity. These results suggest that the isoflavone structure and 5-hydroxyl group are crucial for the cytotoxic properties and that glycosides are inactive. Moreover, tectorigenin induced differentiation of human promyelocytic leukemia HL-60 cells to granulocytes and monocytes/macrophages, and caused apoptotic changes of DNA in the cells, as did genistein. Tectorigenin also inhibited autophosphorylation of epidermal growth factor (EGF) receptor by EGF and decreased the expression of Bcl-2 protein, with less activity than genistein. From these results, tectorigenin may be a possible therapeutic agent for leukemia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Apoptosis / drug effects*
  • Blotting, Western
  • Cell Differentiation / drug effects*
  • Cell Division / drug effects
  • DNA Fragmentation / drug effects
  • Flow Cytometry
  • Gene Expression / drug effects
  • Genes, bcl-1 / drug effects
  • Genistein / chemistry
  • Genistein / pharmacology
  • HL-60 Cells
  • Humans
  • Isoflavones / pharmacology*
  • Phosphorylation
  • Plants, Medicinal / chemistry*
  • Pueraria / chemistry*
  • Spectrometry, Fluorescence
  • Structure-Activity Relationship

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Isoflavones
  • tectorigenin
  • Genistein