IDENTIFICATION OF A CLASS-3 ALDEHYDE DEHYDROGENASE IN HUMAN SALIVA AND INCREASED LEVELS OF THIS ENZYME, GLUTATHIONE S-TRANSFERASES, AND DT-DIAPHORASE IN THE SALIVA OF SUBJECTS WHO CONTINUALLY INGEST LARGE QUANTITIES OF COFFEE OR BROCCOLI
L. Sreerama et al., IDENTIFICATION OF A CLASS-3 ALDEHYDE DEHYDROGENASE IN HUMAN SALIVA AND INCREASED LEVELS OF THIS ENZYME, GLUTATHIONE S-TRANSFERASES, AND DT-DIAPHORASE IN THE SALIVA OF SUBJECTS WHO CONTINUALLY INGEST LARGE QUANTITIES OF COFFEE OR BROCCOLI, Clinical cancer research, 1(10), 1995, pp. 1153-1163
Human saliva was tested for the presence of cytosolic class 3 aldehyde
dehydrogenase, glutathione S-transferases alpha, mu, and pi, and DT-d
iaphorase, enzymes that are known to catalyze the biotransformation of
many xenobiotics, including some that are carcinogens and some that a
re antineoplastic agents, Each of these enzymes was found to be presen
t in this fluid, Inducers of these enzymes are known to be abundantly
present in the human diet, especially in certain vegetables and fruits
, Further investigation revealed that the salivary content of these en
zymes rapidly, coordinately, and markedly increased upon daily consump
tion of relatively large amounts of coffee or broccoli, The enzyme act
ivities of interest rapidly returned to basal levels when these substa
nces were removed from the diet, Given the important role that cytosol
ic class 3 aldehyde dehydrogenase, the glutathione S-transferases, and
DT-diaphorase are thought to play in determining the carcinogenic pot
ential of some cancer-producing agents as,yell as the cytotoxic potent
ial of some antineoplastic agents, and assuming that their salivary le
vels reflect their tissue levels, quantification of the salivary conte
nt of one or more of these enzymes, a noninvasive and relatively easy
undertaking, could be useful in: (a) preliminarily assessing the chemo
preventive potential of various diets and drugs; (b) establishing the
optimal dose and schedule in Phase I clinical trials for any putativel
y chemopreventive diets or drugs of interest; and (c) the rational sel
ection and use of chemotherapeutic agents, since several are inactivat
ed, and a few are activated, by these enzymes; alternatively, the anti
neoplastic agent could be selected first and then a diet that enables
the agent to achieve its full therapeutic potential would be selected
based on whether high or low enzyme activity would be favorable in tha
t regard, Such measurements may also be useful as an indicator when ex
posure to carcinogenic/teratogenic/otherwise toxic environmental/indus
trial/dietary agents that induce these enzymes is suspected.