The majority prostate cancers are indolent and do not affect patient's survivals, yet the patients are subjected to overtreatment suffering from treatment side effects, affecting patient's quality of life. Current cancer characters such as grade, stage, serum PSA and nomogram only predict clinical behavior to a certain degree, and do not sufficiently distinguish patients with aggressive (e.g. metastatic) or less aggressive tumors. Developing biomarkers to accurately stratify these patients become urgent task. Thus we propose to use systematic approaches to define protein and pathway network signatures that can distinguish indolent and a form of aggressive, metastatic, prostate cancer applying our Novel Proteomic Pathway array integrated with genomics via bioinformatics. Specifically, we will use a novel proteomic pathway array to identify proteins in key cellular signaling pathways that are differentially expressed or phosphorylated in non-metastatic vs. cancer with metastatic potential. Next, we will determine the association of signal pathway proteins with the clinical outcome of metastasis using high throughput tissue micro arrays. The functional relevance of the proteins identified will be tested in vitro and in vivo. Overall this study uses a unique proteomics and systems biology approach to identifying new biomarkers, and possible therapeutic targets, for metastatic prostate cancer through the elucidation of distinct regulatory network that underlies the biology of the prostate cancer. The advantage of combined expertise of our highly productive and collaborative researchers integrating various high through proteomic and genomic platform with innovative bioinformatics approaches will ensure the successful execution of this proposal. The biomarkers identified from this proposal will greatly improve current strategies to stratify prostate cancer patients between non-metastatic and metastatic disease.

Public Health Relevance

This study will lead to the discovery of novel signal pathway proteins and networks associated with indolent or aggressive (metastatic) prostate cancer and will generate clinically relevant information that may lead to the development of biomarkers for early detection of aggressive prostate cancer. The functional study of these signal transduction proteins may lead to development of novel pathway based treatment strategies for prostate cancer. These research activities are vital to reducing the cancer outcome gaps.

Agency
National Institute of Health (NIH)
Institute
Veterans Affairs (VA)
Type
Non-HHS Research Projects (I01)
Project #
1I01BX001505-01A3
Application #
8543334
Study Section
Oncology A (ONCA)
Project Start
2013-10-01
Project End
2017-09-30
Budget Start
2013-10-01
Budget End
2014-09-30
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
VA Medical Center
Department
Type
DUNS #
070501002
City
New York
State
NY
Country
United States
Zip Code
10010