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Journal of Biomedical Science





Vol. 8, No. 2, 2001   

Free Abstract     Article (References)     Article (PDF 315 KB)     

Original Paper

Genistein Effects on Growth and Cell Cycle of Candida albicans
Ali Yazdanyar, Michael Essmann, Bryan Larsen

Des Moines University Osteopathic Medical Center, Des Moines, Iowa, USA

Address of Corresponding Author

Journal of Biomedical Science 2001;8:153-159 (DOI: 10.1159/000054027)


 goto top of page Key Words

  • Candida
  • Virulence
  • Estradiol
  • Genistein
  • Nafoxidine

 goto top of page Abstract

Microbial virulence is generally considered to be multifactorial with infection resulting from the sum of several globally regulated virulence factors. Estrogen may serve as a signal for global virulence induction in Candida albicans. Nonsteroidal estrogens and estrogen receptor antagonists may therefore have interesting effects on yeast and their virulence factors. Growth of C. albicans was monitored by viable plate counts at timed intervals after inoculation into yeast nitrogen broth plus glucose. To determine if increased growth of yeast in the presence of estradiol was due to tyrosine kinase-mediated signaling, we measured growth in the presence of genistein, estradiol or genistein plus estradiol and compared these conditions to controls, which were not supplemented with either compound. Unexpectedly, genistein stimulated growth of C. albicans. In addition, genistein was found to increase the rate of germination (possibly reflecting release from G0 into G1 cell cycle phase) and also increased Hsp90 expression, demonstrated by a dot blot technique which employed a commercial primary antibody detected with chemiluminescence with horseradish peroxidase-labeled secondary antibody. These biological effects may be attributable to genistein's activity as a phytoestrogen. In contrast, nafoxidine suppressed growth of Candida and mildly diminished Hsp90 expression. This study raises the possibility of receptor cross-talk between estrogen and isoflavinoid compounds, and antiestrogens which may affect the same signaling system, though separate targets for each compound were not ruled out.

Copyright © 2001 National Science Council, ROC and S. Karger AG, Basel


 goto top of page Author Contacts

Bryan Larsen, PhD
Dean for University Research
Des Moines University Osteopathic Medical Center
3200 Grand Avenue, Des Moines, IA 50312 (USA)
Tel. +1 515 271 1559, Fax +1 515 271 1644, E-Mail bryan.larsen@dmu.edu


 goto top of page Article Information

Received: Received: July 7, 2000
Accepted: August 28, 2000
Number of Print Pages : 7
Number of Figures : 7, Number of Tables : 0, Number of References : 15

 
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