Prostate cancer is the second leading cause of cancer death in the United States. The primary cause ofmortality is distant metastatic disease for which androgen deprivation is the initial therapeutic standard.However, virtually all patients treated with androgen deprivation will progress in a predictable and irreversiblemanner to androgen independence and hormone refractory state.The wide spread use of PSA in the clinic has altered the profile of patients with hormone-refractory prostatecancer. The spectrum now encompasses patients with marked differences in disease burden and symptomswith three main categories of patients that can be identified: Non- metastatic androgen independent diseasewith rising PSA (i.e. PSA-only disease), rising PSA with stable metastatic disease, and increasing PSA withobjective progression. Although historically the role of systemic therapy has been palliative in this stage of thedisease, progress in drug development has led to investigating the impact of chemotherapy on survival. Eventhough it is likely that taxane-based chemotherapy may have an impact on survival, the effect nonetheless isnot optimal in that it is complicated by toxicities and has doubtful curative potential. As with any metastaticcancer, the ultimate goals of therapy in this setting are clear: to prolong life, to decrease morbidity, and toincrease quality of life. Therefore it is particularly important to investigate alternative novel approaches thatstem from observation on the biology of the disease

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center (P50)
Project #
2P50CA069568-11
Application #
7680672
Study Section
Special Emphasis Panel (ZCA1-RPRB-M (J1))
Project Start
2008-08-21
Project End
2013-05-31
Budget Start
2008-08-21
Budget End
2009-05-31
Support Year
11
Fiscal Year
2008
Total Cost
$59,209
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
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Xie, Yuanyuan; Cao, Zhen; Wong, Elissa Wp et al. (2018) COP1/DET1/ETS axis regulates ERK transcriptome and sensitivity to MAPK inhibitors. J Clin Invest 128:1442-1457
Singhal, Udit; Wang, Yugang; Henderson, James et al. (2018) Multigene Profiling of CTCs in mCRPC Identifies a Clinically Relevant Prognostic Signature. Mol Cancer Res 16:643-654
Wang, Xiaoju; Qiao, Yuanyuan; Asangani, Irfan A et al. (2017) Development of Peptidomimetic Inhibitors of the ERG Gene Fusion Product in Prostate Cancer. Cancer Cell 31:532-548.e7
Blattner, Mirjam; Liu, Deli; Robinson, Brian D et al. (2017) SPOP Mutation Drives Prostate Tumorigenesis In Vivo through Coordinate Regulation of PI3K/mTOR and AR Signaling. Cancer Cell 31:436-451
Dai, Xiangpeng; Gan, Wenjian; Li, Xiaoning et al. (2017) Prostate cancer-associated SPOP mutations confer resistance to BET inhibitors through stabilization of BRD4. Nat Med 23:1063-1071
Lin, Ke-Chih; Torga, Gonzalo; Wu, Amy et al. (2017) Epithelial and mesenchymal prostate cancer cell population dynamics on a complex drug landscape. Converg Sci Phys Oncol 3:
Chen, Weiqiang; Allen, Steven G; Reka, Ajaya Kumar et al. (2016) Nanoroughened adhesion-based capture of circulating tumor cells with heterogeneous expression and metastatic characteristics. BMC Cancer 16:614
Hu, Shuhuan; Liu, Guangyu; Chen, Weiqiang et al. (2016) Multiparametric Biomechanical and Biochemical Phenotypic Profiling of Single Cancer Cells Using an Elasticity Microcytometer. Small 12:2300-11
Piert, Morand; Montgomery, Jeffrey; Kunju, Lakshmi Priya et al. (2016) 18F-Choline PET/MRI: The Additional Value of PET for MRI-Guided Transrectal Prostate Biopsies. J Nucl Med 57:1065-70

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