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Isoflavones inhibit intestinal epithelial cell proliferation and induce apoptosis in vitro
C Booth1, D F Hargreaves, J A Hadfield
1Epithelial Biology Group, Paterson Institute for Cancer Research, Christie Hospital NHS Trust, Manchester, UK.
Abstract:
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.
Insights
Soy isoflavones, like genistein, inhibit intestinal cell growth and promote cell death. These compounds may help prevent colon cancer and slow tumor development by reducing proliferation and inducing apoptosis.
Area of Science:
- Biochemistry
- Molecular Biology
- Cancer Research
Background:
- High intake of soya-based diets is linked to reduced cancer risk.
- Isoflavones, particularly genistein from soy, possess protein tyrosine kinase (PTK) inhibitory and hormonal properties.
Purpose of the Study:
- To investigate the effects of genistein and novel synthetic isoflavones on normal and cancerous intestinal epithelial cells.
- To compare the activity of isoflavones with known inhibitors like oestradiol, tamoxifen, and tyrphostin.
Main Methods:
- Exposure of normal (IEC6, IEC18) and transformed (SW620, HT29) intestinal cell lines to genistein and synthetic isoflavones.
- Assessment of cell proliferation, apoptosis, and protein tyrosine kinase (PTK) inhibitory activity.
Main Results:
- Genistein and tamoxifen significantly inhibited cell proliferation.
- Seven novel isoflavones showed activities comparable to genistein.
- Isoflavones induced apoptosis and, except for one, exhibited PTK inhibitory activity.
Conclusions:
- Isoflavones reduce intestinal cell proliferation and induce apoptosis, potentially through PTK inhibition.
- These actions suggest a role for isoflavones in protecting intestinal epithelium and reducing colon tumor growth.