Abstract
Epidemiological and laboratory studies
provide insight into the anticarcinogenic potential of garlic and its
constituent compounds.
Both water- and lipid-soluble allyl sulfur
compounds are effective in blocking a myriad of chemically induced
tumors. Part
of the protection from these compounds probably
relates to a block in nitrosamine formation and metabolism. However,
blockage
in the initiation and promotion phases of the
carcinogenicity of various compounds, including polycyclic hydrocarbons,
provide
evidence that garlic and its constituents can alter
several phase I and II enzymes. Their ability to block experimentally
induced tumors in a variety of sites including
skin, mammary and colon, suggests a general mechanism of action. Changes
in
DNA repair and in immunocompetence may also account
for some of this protection. Some, but not all, allyl sulfur compounds
can also effectively retard tumor proliferation and
induce apoptosis. Changes in cellular thiol and phosphorylation stains
may account for some of these antitumorigenic
properties. The anticarcinogenic potential of garlic can be influenced
by several
dietary components including specific fatty acids,
selenium, and vitamin A. Since garlic and its constituents can suppress
carcinogen formation, carcinogen bioactivation, and
tumor proliferation it is imperative that biomarkers be established to
identify which individuals might benefit most and
what intakes can occur with ill consequences..
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