Accession Number:

ADA612827

Title:

Identification of Novel, Inherited Genetic Markers for Aggressive PCa in European and African Americans Using Whole Genome Sequencing

Descriptive Note:

Annual rept. 22 Aug 2012-21 Aug 2013

Corporate Author:

WAKE FOREST UNIV WINSTON-SALEM NC SCHOOL OF HEALTH SCIENCES

Personal Author(s):

Report Date:

2013-09-01

Pagination or Media Count:

16.0

Abstract:

Prostate cancer PCa is the most common cancer and the second leading cause of cancer death among men in the United States. While most prostate cancer patients have an indolent form of the disease that may not even require treatment, about 10-15 of PCa patients have an aggressive form that may progress to metastases and death, thus requiring intensive treatment. Several clinical variables such as PSA levels, Gleason grade and TNM stage are good predictors for disease with poor clinical outcomes however, their predictive performance needs to be improved. Our inability to reliably distinguish between these two forms of PCa, early on in the course of the disease has resulted in the over-treatment of many and under treatment of some. The identification of additional markers, including genetic variants will improve our ability to distinguish aggressive from indolent forms of PCa and to better understand the racial disparity of PCa that exists between European Americans EA and African Americans AA. In this DOD proposal, we hypothesized that multiple rare sequence variants in the genome may increase aggressive PCa risk. Through a genome-wide search of rare variants based on an existing population from Johns Hopkins Hospital JHH of 600 aggressive PCa patients and 600 indolent PCa patients using Illuminas Human Exome BeadChip, we identified several rare variants that are significantly associated with aggressive PCa development in EA or AA populations. The implicated rare variants will be followed in additional populations.

Subject Categories:

  • Genetic Engineering and Molecular Biology
  • Medicine and Medical Research

Distribution Statement:

APPROVED FOR PUBLIC RELEASE