Soy isoflavonoids and cancer - metabolism at the target site

Citation
Bj. Boersma et al., Soy isoflavonoids and cancer - metabolism at the target site, MUT RES-F M, 480, 2001, pp. 121-127
Citations number
36
Categorie Soggetti
Molecular Biology & Genetics
Journal title
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
ISSN journal
13861964 → ACNP
Volume
480
Year of publication
2001
Pages
121 - 127
Database
ISI
SICI code
1386-1964(20010901)480:<121:SIAC-M>2.0.ZU;2-K
Abstract
Isoflavonoids are members of the broad class of plant polyphenols that have been shown in vivo to have benefit in the prevention of a wide variety of chronic diseases, including cancer. For genistein (5,7,4 ' -trihydroxyisofl avone) (GEN), the major isoflavone in soy, reported mechanisms for these bi ological activities are numerous and include regulation of estrogen-mediate d events, inhibition of tyrosine kinase and DNA topoisomerase activities, s ynthesis and release of TGF beta, and modulation of apoptosis. However, the biochemical effects of GEN in cell culture occur at concentrations in the micromolar range, far above the circulating levels of the unconjugated GEN. This may point to the limitations of cell culture for the evaluation of th e activity and mechanisms of potential anti-carcinogens. GEN is extensively metabolized in vivo, with only about 14-16% excreted in an unmodified form . Metabolism may also occur because of interaction between GEN (as well as other polyphenols) and oxidants produced by inflammatory cells (HOCl, HOBr and ONOO-). These react with GEN to form brominated, chlorinated and/or nit rated GEN. Emerging evidence indicates that these modifications may substan tially increase the biological activities of the parent compound. Future in vestigations of GEN and other polyphenols must, therefore, take into accoun t metabolism at the tissue site. (C) 2001 Elsevier Science B.V. All rights reserved.