Metastasis, especially to the bone, is the most significant cause of morbidity and mortality in prostate cancer? patients. Therefore, development of relevant metastasis models for prostate cancer is of critical importance? for delineating the molecular mechanism underlining this process.? ? In our preliminary studies, we showed that omega-3 (n-3) polyunstatured fatty acids (PUFAs) can inhibit the? progression of prostate cancer in a Pten knockout mouse model, and increase survival of tumor-bearing? animals. However, the effect of n-3 PUFA on prostate cancer metastasis was not assessed. Epidemiological? data suggest that higher consumption of fish, a rich source of n-3 PUFA, is strongly associated with a? reduced risk of metastatic prostate cancer.? ? In this proposal, we will develop an animal model for spontaneous prostate cancer metastasis, and use this? model to determine the potential effect of n-3 PUFA on metastasis.? ? Aim 1. Develop a quantitative, live-observable model of prostate cancer metastasis. Enhanced yellow? fluorescent protein (EYFP) and lacZ markers will be used for live-monitoring and quantification of tumor? burden, respectively, at the primary tumor site and at the site of metastases. The transgenes will be? introduced into prostate-specific Pten knockout mice that mimic well the clinical course of human prostate? cancer, from prostatic intraepithelial neoplasia, carcinoma in situ, invasive carcinoma to metastasis. The? EYFP and LacZ markers will be expressed only in prostate tumor cells. Importantly, their levels of expression? will not be reduced or extinguished overtime or when prostate tumor cells metastasize to other organs such? as the bone, lung, and lymph nodes.? ? Aim 2. Determine the effect of dietary n-3 fatty acid supplement on prostate cancer metastasis.? Animals will be fed with diets containing various amounts of n-3 PUFA. Development of cancer in the? prostate and metastasis in the lung, inguinal lymph nodes and tibia/femur will be monitored. Tumor burden? will be quantified.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21CA124511-01
Application #
7176369
Study Section
Chemo/Dietary Prevention Study Section (CDP)
Program Officer
Kim, Young Shin
Project Start
2007-05-01
Project End
2009-04-30
Budget Start
2007-05-01
Budget End
2008-04-30
Support Year
1
Fiscal Year
2007
Total Cost
$147,833
Indirect Cost
Name
Wake Forest University Health Sciences
Department
Biology
Type
Schools of Medicine
DUNS #
937727907
City
Winston-Salem
State
NC
Country
United States
Zip Code
27157
Wang, Shihua; Wu, Jiansheng; Suburu, Janel et al. (2012) Effect of dietary polyunsaturated fatty acids on castration-resistant Pten-null prostate cancer. Carcinogenesis 33:404-12
Wang, Lei; Chen, Wei; Feng, Yun et al. (2011) Genome characterization of the oleaginous fungus Mortierella alpina. PLoS One 6:e28319