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New Compound Protects Against Certain Cancers
Researchers identified a new compound called CDDO-Im that protects against the development of liver cancer in laboratory animals. The compound stimulates the enzymes that remove toxic substances from the cells and increases the cells' resistance to cancer-causing toxins.
In a two-year study, investigators from Johns Hopkins Bloomberg School of Public Health in Baltimore studied the effectiveness of low doses of CDDO-Im in preventing cancers in laboratory rats.
They believe the compound may be particularly effective in preventing cancers with a strong inflammatory component, such as liver, colon, prostate and gastric cancers.
"This compound has a much greater effect at a far lower dose than any other compound currently used for preventing aflatoxin-induced cancer in humans," says Thomas Kensler, Ph.D., a cancer biologist at the Johns Hopkins Bloomberg School of Public Health.
The synthetic compound is derived from oleanolic acid -- a naturally occurring substance found in plants all over the world. Other oleanolic derivatives show marked anti-tumor activity in both animals and humans. Like those other compounds, CDDO-Im also has strong anti-inflammatory properties, making it ideally suited to prevent certain cancers.
Due to the compound's ability to stimulate the body's cancer-fighting capabilities at such low doses, Kensler believes CDDO-Im is an excellent candidate for cancer prevention use in humans.
"If this compound can produce such a potent and dramatic reduction in the number of pre-cancerous growths, it should have an equally dramatic impact on the development of actual cancers," he says.
Along with serving as a valuable tool in the development of new cancer prevention interventions, CDDO-Im may offer protection in a wide range of other disease settings, including neurodegenerative disease, asthma and emphysema.
This article was reported by Ivanhoe.com, who offers Medical Alerts by e-mail every day of the week. To subscribe, go to: http://www.ivanhoe.com/newsalert/.
SOURCE: Cancer Research, 2006;66:1-7
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