This application represents the creation of a Specialized Program of Research Excellence (SPORE) in Prostate Cancer originating from the Prostate Cancer Program of the newly configured Dana-Farber Harvard Cancer Center (DF/HCC). The DF/HCC Prostate Cancer SPORE includes investigators from all the Harvard affiliated hospitals; The Beth Israel Deaconess Hospital, the Brigham & Women's Hospital, the Dana-Farber Cancer Institute, the Massachusetts General Hospital, and the Harvard School of Public Health. Five major projects are supported through this application including: 1) Genetic and serological markers of the PI3/Kinase Akt pathway in prostate cancer; 2) the peroxisome proliferator activator receptor gamma as a target for prostate cancer therapy; 3) the genetic classification of prostate cancer; 4) Expression analysis prediction of prostate cancer outcome; and 5) the androgen receptor in hormone refractory prostate cancer. These projects will be integrated by the creation of four cores. These are: 1) Administration, evaluation, and planning; 2) Biostatistics; 3) Tissue and Pathology; and 4) Genomics. This SPORE application outlines a Developmental Projects Program that includes a plan for selection of new projects as well as seven pilot projects that could be supported. We also include a Career Development Award Program that outlines a mechanism for the identification and support of talented young investigators in prostate cancer. The overall goal of the DFHCC SPORE is the translation of biological and technological advances into clinically meaningful advances for men with prostate cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center (P50)
Project #
5P50CA090381-03
Application #
6762452
Study Section
Special Emphasis Panel (ZCA1-GRB-V (M1))
Program Officer
Hruszkewycz, Andrew M
Project Start
2002-09-19
Project End
2007-04-30
Budget Start
2004-05-20
Budget End
2005-04-30
Support Year
3
Fiscal Year
2004
Total Cost
$2,534,537
Indirect Cost
Name
Dana-Farber Cancer Institute
Department
Type
DUNS #
076580745
City
Boston
State
MA
Country
United States
Zip Code
02215
Dickerman, Barbra A; Torfadottir, Johanna E; Valdimarsdottir, Unnur A et al. (2018) Midlife metabolic factors and prostate cancer risk in later life. Int J Cancer 142:1166-1173
McKay, Rana R; Werner, Lillian; Jacobus, Susanna J et al. (2018) A phase 2 trial of abiraterone acetate without glucocorticoids for men with metastatic castration-resistant prostate cancer. Cancer :
Larimer, Benjamin M; Bloch, Emily G; Nesti, Sarah et al. (2018) The Effectiveness of Checkpoint Inhibitor Combinations and Administration Timing Can Be Measured by Granzyme B PET Imaging. Clin Cancer Res :
Barber, Lauren; Gerke, Travis; Markt, Sarah C et al. (2018) Family History of Breast or Prostate Cancer and Prostate Cancer Risk. Clin Cancer Res 24:5910-5917
Chen, Sen; Cai, Changmeng; Sowalsky, Adam G et al. (2018) BMX-Mediated Regulation of Multiple Tyrosine Kinases Contributes to Castration Resistance in Prostate Cancer. Cancer Res 78:5203-5215
Pakula, Hubert; Linn, Douglas E; Schmidt, Daniel R et al. (2018) Protocols for Studies on TMPRSS2/ERG in Prostate Cancer. Methods Mol Biol 1786:131-151
Elfandy, Habiba; Armenia, Joshua; Pederzoli, Filippo et al. (2018) Genetic and Epigenetic Determinants of Aggressiveness in Cribriform Carcinoma of the Prostate. Mol Cancer Res :
Han, W; Gao, S; Barrett, D et al. (2018) Reactivation of androgen receptor-regulated lipid biosynthesis drives the progression of castration-resistant prostate cancer. Oncogene 37:710-721
Stopsack, Konrad H; Gonzalez-Feliciano, Amparo G; Peisch, Samuel F et al. (2018) A Prospective Study of Aspirin Use and Prostate Cancer Risk by TMPRSS2:ERG Status. Cancer Epidemiol Biomarkers Prev 27:1231-1233
Russo, Joshua W; Liu, Xiaming; Ye, Huihui et al. (2018) Phosphorylation of androgen receptor serine 81 is associated with its reactivation in castration-resistant prostate cancer. Cancer Lett 438:97-104

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