Planta Med 2005; 71(6): 489-494
DOI: 10.1055/s-2005-864147
Original Paper
Pharmacology
© Georg Thieme Verlag KG Stuttgart · New York

The Benzophenanthridine Alkaloid Fagaronine Induces Erythroleukemic Cell Differentiation by Gene Activation

Claude Dupont1 , Eric Couillerot2 , Reynald Gillet1 , Catherine Caron3 , Monique Zeches-Hanrot3 , Jean-François Riou1 , Chantal Trentesaux1
  • 1JE 2428 Onco-Pharmacologie, UFR Pharmacie, IFR 53 Biomolécules, Université de Reims Champagne-Ardenne, Reims, France
  • 2Laboratoire de Stress, Défenses et Reproduction des Plantes, URVVC EA2069, UFR Sciences, Université de Reims Champagne-Ardenne, Reims, France
  • 3Laboratoire de Pharmacognosie, FRE 2715 CNRS UFR Pharmacie, Université de Reims Champagne-Ardenne, Reims, France
Further Information

Publication History

Received: August 9, 2004

Accepted: January 6, 2005

Publication Date:
21 June 2005 (online)

Abstract

Fagaronine, a benzophenanthridine alkaloid from Fagara zanthoxyloides Lam. (Rutaceae), has been tested on the erythroleukemic cell line K562 in order to explain some previous results on cell differentiation. In this study we showed that fagaronine induces a significant hemoglobinization of the human erythroleukemic cell line K562. This hemoglobin synthesis was accompanied by a strong increase of erythroid mRNA expression such as γ- and α-globin, and PBGD, an enzyme of heme synthesis. In addition, the Epo-R transcripts were also stimulated indicating that cells are engaged in a maturation process. Both transcription factors GATA-1 and NF-E2, which play an important role in the regulation of genes involved in the erythroid differentiation, were also transcriptionally up-regulated. To elucidate the possible role of GATA-1 in the FAG-induced differentiation of K562 cells, we transfected reporter constructs containing regulatory regions of erythroid genes encompassing GATA-1 binding sites. After 48 hours of treatment, FAG stimulated the EPO-R and γ-globin promoters by 2- to 3-fold and the promoter/enhancer region of GATA-1 gene by 3.2-fold. A mutation within the GATA-1 binding sites strongly decreased the promoter activation induced by FAG. Taken together, our results represent a demonstration that FAG exerts its differentiating activity by a specific activation of the regulating GATA-1 regions of genes involved in the erythroid phenotype expression.

Abbreviations

ACLA:aclacinomycin

FAG:fagaronine

PBGD:porphobilinogene deaminase

EPO-R:erythropoietin receptor

GAPDH:glyceraldehydes 3-phosphate dehydrogenase

FCS:fetal calf serum

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Chantal Trentesaux

JE 2428 Onco-Pharmacologie

UFR Pharmacie

IFR 53 Biomolécules

Université de Reims Champagne-Ardenne

51 rue Cognacq Jay

51096 Reims cedex

France

Phone: +33-326-918-045

Fax: +33-326-918926

Email: chantal.trentesaux@univ-reims.fr

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