DESCRIPTION: (Adapted from Applicant's Abstract). The leading risk factor
for lung cancer in the U.S. is cigarette smoking. The incidence of lung
cancer remains alarmingly high and, despite the use of modern diagnostic and
treatment modalities, the overall cure rate is low. Thus, preventive
efforts, based upon the understanding of risk factors may be of paramount
importance in controlling this deadly disease. A minority of smokers
develops lung cancer, suggesting variability in disease susceptibility.
Smoking itself may contribute to a causal complex along with other
contributing factors such as genetic predisposition. Moreover, only a small
proportion of all cancers is explained by simple monogenic inheritance.
Several polymorphisms in the genes responsible for either activation or
deactivation of carcinogens have been reported to be associated with lung
cancer risk. To date, however, no studies have had sufficient statistical
power to examine a number of complex gene-environment interactions in lung
cancer (e.g., dietary and occupational contributions or gene-gene
interactions).
A large molecular epidemiologic study is proposed to examine six polymorphic
traits in metabolism and lung cancer risk and how this risk may be modified
by dietary or occupational exposures. The application posits that the
combination of traits which enhance activation of carcinogenic metabolites
and decrease detoxification of reactive products will confer excess risk in
current and former smokers. Furthermore, it suggests that this risk will be
modified by diet and occupational exposures. It is intended that a better
understanding of these risks and their modification could lead to more
effective preventive strategies.
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