Smoking is the major cause of upper aerodigestive tract cancers. Among
the many constituents of tobacco smoke, polynuclear aromatic hydrocar
bons and tobacco-specific nitrosamines are strongly implicated as caus
ative factors for these cancers. The probability that these compounds
will induce cancer in a given individual will depend on that person's
ability to metabolically activate or detoxify them. Chronic production
of DNA damage by these metabolically activated carcinogens is consist
ent with current concepts of carcinogenesis in which multiple genetic
changes, such as activation of oncogenes or inactivation of tumor supp
ressor genes, appear to be critical. Chemopreventive agents which decr
ease the level of DNA damage should therefore decrease the risk for ca
ncer. Biomarkers such as carcinogen-DNA adducts, carcinogen-hemoglobin
adducts, and urinary metabolites of carcinogens will indicate the amo
unt of metabolically activated carcinogen which may damage DNA in an i
ndividual and can therefore be used as an index of risk. Selected biom
arkers are discussed in this paper. These biomarkers of internal dose
have great potential for application in chemoprevention trials. (C) 19
93 Wiley-Uss, Inc.