Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
3871511 | The Journal of Urology | 2009 | 6 Pages |
Abstract
Sequence variants along 17q12 and 17q24 were present in a significantly higher proportion of our prostate cancer cases than in our controls. Adverse pathological features, including higher Gleason grade and pathological stage, were more frequent in 17q12 carriers. Since these alleles may act in conjunction with variants on other chromosomes to influence prostate cancer risk, additional research is required to determine the cumulative associations of genetic risk variants with prognosis.
Keywords
Related Topics
Health Sciences
Medicine and Dentistry
Nephrology
Authors
Brian T. Helfand, Stacy Loeb, Joshua J. Meeks, Angela J. Fought, Donghui Kan, William J. Catalona,