Grant Number:	4R01CA135008-03 Interpret this number
Primary Investigator:	Liu, Wennuan
Organization:	Wake Forest University Health Sciences
Project Title:	Interaction of Germline and Somatic Changes in PCA Progression
Fiscal Year:	2011

DESCRIPTION (provided by applicant): Interaction of germline and somatic changes in PCa progression Abstract Recent successes in discovering germline variants associated with prostate cancer (PCa) risk is encouraging. However, whether these risk variants play role in PCa progression is unclear. Understanding factors associated with the progression of PCa will have a significant impact on management and treatment of the disease. We hypothesize that germline risk variants, combined with somatic genetic and epigenetic changes may increase the risk of prostate cancer progression. To test this hypothesis and to uncover the genetic and epigenetic markers of the complex mechanisms underlining the progression and poor clinical outcome of PCa, we present three specific aims with integrated and novel analytic approaches in this proposal. First, for the genomic regions where germline variants are associated with PCa risk, we will screen for potential germline CNVs, somatic DNA copy number changes and/or methylation modifications among 96 PCa patients who have developed progressed disease. Several novel global DNA copy number and methylation detection methods will be employed to examine DNA samples isolated from frozen tumor and normal prostate tissues. Secondly, we will test whether known germline PCa risk variants, when combined with somatic DNA changes and/or methylation modifications identified in Aim 1, are associated with increased risk for PCa progression in an existing and well-designed study population from Johns Hopkins Hospital, including 800 pairs of progressors and matched non-progressors. Finally, we will identify genes whose protein expression levels are associated with genetic and epigenetic alterations that are implicated in Aim 2. The results of this study may advance our understanding on the etiology of PCa progression and augment current methods to better predict which PCa patients are most likely to develop progressed disease at the time of diagnosis. The PCa patients with poor prognosis can receive intensive monitoring and treatment. PUBLIC HEALTH RELEVANCE: This proposal intends to identify interaction effects on prostate cancer (PCa) progression for several known germline (PCa) risk variants genetic and somatic genetic and epigenetic changes identified in our study, using several global detection methods. The identified genes may advance our understanding on the etiology of PCa progression and augment current methods to better predict which PCa patients are most likely to develop progressed disease at the time of diagnosis. The PCa patients with poor prognosis can receive intensive monitoring and treatment.




Genetic markers associated with early cancer-specific mortality following prostatectomy.
Authors: Liu W. , Xie C.C. , Thomas C.Y. , Kim S.T. , Lindberg J. , Egevad L. , Wang Z. , Zhang Z. , Sun J. , Sun J. , et al. .
Source: Cancer, 2013-07-01 00:00:00.0; 119(13), p. 2405-12.
EPub date: 2013-07-01 00:00:00.0.
PMID: 23609948
Related Citations

DNA methylation alterations exhibit intraindividual stability and interindividual heterogeneity in prostate cancer metastases.
Authors: Aryee M.J. , Liu W. , Engelmann J.C. , Nuhn P. , Gurel M. , Haffner M.C. , Esopi D. , Irizarry R.A. , Getzenberg R.H. , Nelson W.G. , et al. .
Source: Science Translational Medicine, 2013-01-23 00:00:00.0; 5(169), p. 169ra10.
PMID: 23345608
Related Citations

Identification of novel CHD1-associated collaborative alterations of genomic structure and functional assessment of CHD1 in prostate cancer.
Authors: Liu W. , Lindberg J. , Sui G. , Luo J. , Egevad L. , Li T. , Xie C. , Wan M. , Kim S.T. , Wang Z. , et al. .
Source: Oncogene, 2012-08-30 00:00:00.0; 31(35), p. 3939-48.
EPub date: 2012-08-30 00:00:00.0.
PMID: 22139082
Related Citations

DIAPH3 governs the cellular transition to the amoeboid tumour phenotype.
Authors: Hager M.H. , Morley S. , Bielenberg D.R. , Gao S. , Morello M. , Holcomb I.N. , Liu W. , Mouneimne G. , Demichelis F. , Kim J. , et al. .
Source: Embo Molecular Medicine, 2012 Aug; 4(8), p. 743-60.
PMID: 22593025
Related Citations

Identification of new differentially methylated genes that have potential functional consequences in prostate cancer.
Authors: Kim J.W. , Kim S.T. , Turner A.R. , Young T. , Smith S. , Liu W. , Lindberg J. , Egevad L. , Gronberg H. , Isaacs W.B. , et al. .
Source: Plos One, 2012; 7(10), p. e48455.
PMID: 23119026
Related Citations