Cargando…
Isoflavones inhibit intestinal epithelial cell proliferation and induce apoptosis in vitro
There have been many reports that high soya-based diets reduce the risk of certain types of cancer. This effect may be due to the presence of high levels of isoflavones derived from the soya bean, particularly genistein which has been shown to be a protein tyrosine kinase (PTK) inhibitor and have bo...
Autores principales: | , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1999
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363089/ https://www.ncbi.nlm.nih.gov/pubmed/10408396 http://dx.doi.org/10.1038/sj.bjc.6690559 |
_version_ | 1782153617290035200 |
---|---|
author | Booth, C Hargreaves, D F Hadfield, J A McGown, A T Potten, C S |
author_facet | Booth, C Hargreaves, D F Hadfield, J A McGown, A T Potten, C S |
author_sort | Booth, C |
collection | PubMed |
description | There have been many reports that high soya-based diets reduce the risk of certain types of cancer. This effect may be due to the presence of high levels of isoflavones derived from the soya bean, particularly genistein which has been shown to be a protein tyrosine kinase (PTK) inhibitor and have both oestrogenic and anti-oestrogenic properties. We have examined the effect of genistein and a number of novel synthetic analogues on both normal (IEC6, IEC18) and transformed (SW620, HT29) intestinal epithelial cell lines. Responses were compared to those elicited by oestradiol, the anti-oestrogen tamoxifen, and the tyrosine kinase inhibitor tyrphostin. Genistein and tamoxifen were potent inhibitors of cell proliferation. Of seven novel isoflavones tested, none were more potent inhibitors than genistein, and all displayed similar relative activities across the different cell lines. In addition to inhibiting cell proliferation, cell death via apoptosis was observed when the cells were exposed to the isoflavones and all but one exhibited PTK inhibitory activity. These data suggest that by reducing proliferation and inducing apoptosis, possibly due in part to PTK inhibition, isoflavones may have a role in protecting normal intestinal epithelium from tumour development (reducing the risk) and may reduce colonic tumour growth. © 1999 Cancer Research Campaign |
format | Text |
id | pubmed-2363089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1999 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23630892009-09-10 Isoflavones inhibit intestinal epithelial cell proliferation and induce apoptosis in vitro Booth, C Hargreaves, D F Hadfield, J A McGown, A T Potten, C S Br J Cancer Regular Article There have been many reports that high soya-based diets reduce the risk of certain types of cancer. This effect may be due to the presence of high levels of isoflavones derived from the soya bean, particularly genistein which has been shown to be a protein tyrosine kinase (PTK) inhibitor and have both oestrogenic and anti-oestrogenic properties. We have examined the effect of genistein and a number of novel synthetic analogues on both normal (IEC6, IEC18) and transformed (SW620, HT29) intestinal epithelial cell lines. Responses were compared to those elicited by oestradiol, the anti-oestrogen tamoxifen, and the tyrosine kinase inhibitor tyrphostin. Genistein and tamoxifen were potent inhibitors of cell proliferation. Of seven novel isoflavones tested, none were more potent inhibitors than genistein, and all displayed similar relative activities across the different cell lines. In addition to inhibiting cell proliferation, cell death via apoptosis was observed when the cells were exposed to the isoflavones and all but one exhibited PTK inhibitory activity. These data suggest that by reducing proliferation and inducing apoptosis, possibly due in part to PTK inhibition, isoflavones may have a role in protecting normal intestinal epithelium from tumour development (reducing the risk) and may reduce colonic tumour growth. © 1999 Cancer Research Campaign Nature Publishing Group 1999-07 /pmc/articles/PMC2363089/ /pubmed/10408396 http://dx.doi.org/10.1038/sj.bjc.6690559 Text en Copyright © 1999 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Regular Article Booth, C Hargreaves, D F Hadfield, J A McGown, A T Potten, C S Isoflavones inhibit intestinal epithelial cell proliferation and induce apoptosis in vitro |
title | Isoflavones inhibit intestinal epithelial cell proliferation and induce apoptosis in vitro |
title_full | Isoflavones inhibit intestinal epithelial cell proliferation and induce apoptosis in vitro |
title_fullStr | Isoflavones inhibit intestinal epithelial cell proliferation and induce apoptosis in vitro |
title_full_unstemmed | Isoflavones inhibit intestinal epithelial cell proliferation and induce apoptosis in vitro |
title_short | Isoflavones inhibit intestinal epithelial cell proliferation and induce apoptosis in vitro |
title_sort | isoflavones inhibit intestinal epithelial cell proliferation and induce apoptosis in vitro |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363089/ https://www.ncbi.nlm.nih.gov/pubmed/10408396 http://dx.doi.org/10.1038/sj.bjc.6690559 |
work_keys_str_mv | AT boothc isoflavonesinhibitintestinalepithelialcellproliferationandinduceapoptosisinvitro AT hargreavesdf isoflavonesinhibitintestinalepithelialcellproliferationandinduceapoptosisinvitro AT hadfieldja isoflavonesinhibitintestinalepithelialcellproliferationandinduceapoptosisinvitro AT mcgownat isoflavonesinhibitintestinalepithelialcellproliferationandinduceapoptosisinvitro AT pottencs isoflavonesinhibitintestinalepithelialcellproliferationandinduceapoptosisinvitro |