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Imagine going around with chronic sunburn on your face: Your muscles hurt
from being tense all the time; it hurts to smile.Your pulse is higher,
too, from the strain. Even though you are able to function, the discomfort
is always there, wearing away at your body, making you vulnerable.
This is what it’s like, on a much smaller scale, for the prostate,
which is prone to inflammation (even though this doesn’t always
cause noticeable symptoms). Cells called inflammatory infiltrates are
immune-system cells that migrate into inflamed tissue. Their job is to
clean up infection, and generally make sure it doesn’t happen again.“These
infiltrates may be there as a response to prostate infection, chemical
or physical damage to the prostate’s epithelium (lining), and even
changing hormone levels within the prostate,” explains Elizabeth
Platz,Sc.D., M.P.H., associate professor of epidemiology, urology and
oncology. Butsometimes, these cells can outstay their wel-come. “If
the inflammatory response per-sists unnecessarily” — creating
a situation ofchronic stress — “it may create an environ-ment
that is conducive to cancer,” she adds.For the last few years, this
possibility hasintrigued scientists, who are actively lookingto answer
this question: “If we can inhibitchronic inflammation, can we reduce
thefuture risk of prostate cancer?”
Scientists have a ready-made population inwhich to start looking —
men taking aspirinor other nonsteroidal anti-inflammatorydrugs (NSAIDS).
These drugs block chemi-cals called cyclo-oxygenase enzymes, whichplay
a key role in the body’s inflammatoryresponse. One large study of
these men foundthat men taking NSAIDS had a 15 percentlower risk of developing
prostate cancer thanmen who weren’t taking them.
Platz, with colleagues at Hopkins and atthe National Institute of Aging,
recentlystudied 1,244 men participating in the Balti-more Longitudinal
Study of Aging, a studybegun more than 40 years ago and involvingabout
1,500 men, who return every otheryear for physical examinations and medicaltests
— including an assessment of their useof prescription and over-the-counter
drugs.The researchers found that men who usedaspirin or other NSAIDS had
a 29 percentlower risk of prostate cancer than men whodid not use these
drugs; this work was pub-lished in the journal Cancer Epidemiology, Biomarkers
& Prevention.
One concern with this study, Platz says,was the possibility that inflammation
dam-ages the epithelial cells, and causes PSA to
| “If we can inhibit
chronic inflam-mation,can we reduce thefuture risk of prostate cancer?” |
leak out of the prostate and into the blood-stream. Did some of these
men have falselylowered PSA scores because they were takingNSAIDS —
in other words, did treatinginflammation actually mask a man’s truePSA
level, and were some cancers not detected because the PSA wasn’t
getting outof the prostate at levels high enough to beconsidered significant?
To address this issue,Platz and colleagues studied 933 of the men who
did not have prostate cancer and who,over the years, had undergone a combinedtotal
of 3,749 PSA tests. In these men, therewas no difference between those
who usedNSAIDS and those who didn’t. “Thus, thelower risk
of prostate cancer in the users ofaspirin and non-aspirin suggests a modest,but
possibly genuine benefit of these anti-inflammatory drugs.”
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