Prostate cancer genomics can we distinguish between indolent and fatal disease using genetic markers 英文参考文献.docVIP
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Prostate cancer genomics can we distinguish between indolent and fatal disease using genetic markers 英文参考文献
Wiklund Genome Medicine 2010,2:45
/content/2/7/45
RE VIE W
Prostate cancer genomics: can we distinguish
between indolent and fatal disease using genetic
markers?
Fredrik Wiklund*
increase with age, with more than 67% of men aged over
Abstract
80 years having prostate cancer at time of death [3].
Prostate cancer is one of the most heritable cancers
in men, and recent genome-wide association studies
have revealed numerous genetic variants associated
with disease. The risk variants identied using case-
control designs that compared unaected individuals
with all types of patients with prostate cancer show
little or no ability to discriminate between indolent
and fatal forms of this disease. This suggests dierent
genetic components are involved in the initiation
as compared with the prognosis of prostate cancer.
Future studies contrasting patients with more and less
aggressive disease, and exploring association with
disease progression and prognosis, should be more
eective in detecting genetic risk factors for prostate
cancer outcome.
ese ?ndings indicate that a high proportion of prostate
tumors are clinically insigni?cant and will never lead to a
lethal outcome. Furthermore, the introduction and
widespread application of prostate-speci?c antigen (PSA)
testing has led to increased detection of early-stage, low-
volume, non-palpable tumors. is has in turn raised
concerns of increased overdiagnosis and unnecessary
treatment of indolent disease [4,5]. To this end, new
strategies to help clinicians distinguish between lethal
and indolent prostate cancer are urgently needed.
Prostate cancer is one of the most heritable cancers in
men and recent studies have revealed numerous genetic
variants associated with this disease. is review will give
an overview of the current knowledge of prostate cancer
genetics, with a special focus on the ability of genetic
variants to predic
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