ng of a
different variant, marked by SNP rs1447295, is also associated with
prostate cancer. The rs1447295 SNP is located nearby on the same
arm of chromosome 8. The old and the new susceptibility loci, or
gene locations, appear to act independently; a change in one region
did not affect the degree of risk conferred by the other. We now
have two significant regions in the same general area that convey
risk for prostate cancer. This will undoubtedly focus
multidisciplinary studies on this stretch of DNA, called 8q24, said
Meredith Yeager, Ph.D., lead author on the study.
The rs1447295 location could be responsible for about seven
percent of prostate cancer cases in white men of north European
descent. Thus, taken together with rs6983267, these two genetic
changes could account for as much as one quarter of prostate cancer
cases in white men. The increased risk conferred by these loci was
observed for all age groups studied.
CGEMS allows us to look systematically across the entire human
genome and search for common genetic variations that confer risk
for prostate cancer, a very common and very complex disease said
Stephen Chanock, M.D., director of NCIs Core Genotyping Facility in
the Advanced Technology Center.
Identification of new regions like 8q24 furthers efforts to
uncover the genetic basis of prostate cancer, which may eventually
lead to more insights into cancer causation in general," added
Gilles Thomas, M.D., Ph.D., lead scientist of CGEMS.
An initial genome-wide association study was conducted in 2,329
men from across the United States who are participating in the NCIs
Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial
(PLCO) that began in 1993. The PLCO analysis compared 1,172 men
with prostate cancer to 1,157 who did not have cancer.
CGEMS results were further confirmed by a number of other
studies, including the American Cancer Society Cancer Prevention
Study II, the Health Professionals Follow-up Study, the
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