Ovarian cancer is the number one gynecologic killer in the United States. New opportunities for diagnosis, prevention, and treatment will be dependent upon an expanded translational research effort. Fox Chase Cancer Center's Specialized Program of Research Excellence (SPORE) in Ovarian Cancer renewal application consists of five translational research projects, a Developmental Research Program, a Career Development Program, and five specialized Cores to support the research programs. These research projects represent a diversity of translational research objectives, including diagnosis, prevention, and treatment: 1) Mechanisms of COX-2 Inhibition in Ovarian Cancer Prevention; 2) AKT as a Biomarker of Ovarian Cancer Progression and a Target for Therapeutic Intervention; 3) Anti-Mullerian Inhibiting Substance Type II Receptor (MISIIR) Immunoconjugates to Detect and Treat Ovarian Cancer; 4) Molecular-targeted Therapy in Ovarian Cancer; 5) Immunotherapy of Ovarian Cancer: Taking Down the Barriers. The last Project is in collaboration with the Abramson Cancer Center of the University of Pennsylvania. A Biological Scientist and an Applied Scientist are Co-Principal Investigators on each Project. The specialized Cores include an Administrative Core, a Biosample and Tissue Procurement Core, an Ovarian Cancer Consortium for Research and Surveillance Core, a Mouse Engineering Core, and a Biostatistics and Data Management Core. Fox Chase Cancer Center has a long-term commitment to research in ovarian cancer and will provide additional institutional resources to support the goals of the SPORE application and will collaborate with other Ovarian SPORE institutions. Senior leadership is directly involved in the SPORE application. The Principal Investigator is the Senior Vice President for Medical Science. The Co-PI is the Program Leader of the CCSG Ovarian Cancer Program, and the President of Fox Chase Cancer Center serves on the Executive Committee. The Ovarian SPORE Program is a multidisciplinary collaboration of laboratory researchers and clinicians focused on decreasing morbidity and mortality from this disease. Based on progress in the initial funding period, the Fox Chase Cancer Center Ovarian SPORE Program is well positioned to accomplish this goal by prevention strategies based on the understanding of ovarian oncogenesis coupled with novel scientifically-based therapeutic approaches.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center (P50)
Project #
5P50CA083638-08
Application #
7115364
Study Section
Special Emphasis Panel (ZCA1-GRB-G (O1))
Program Officer
Arnold, Julia T
Project Start
1999-09-30
Project End
2009-05-31
Budget Start
2006-09-15
Budget End
2007-05-31
Support Year
8
Fiscal Year
2006
Total Cost
$2,308,479
Indirect Cost
Name
Fox Chase Cancer Center
Department
Type
DUNS #
073724262
City
Philadelphia
State
PA
Country
United States
Zip Code
19111
Nacson, Joseph; Krais, John J; Bernhardy, Andrea J et al. (2018) BRCA1 Mutation-Specific Responses to 53BP1 Loss-Induced Homologous Recombination and PARP Inhibitor Resistance. Cell Rep 25:1384
Gabbasov, Rashid; Xiao, Fang; Howe, Caitlin G et al. (2018) NEDD9 promotes oncogenic signaling, a stem/mesenchymal gene signature, and aggressive ovarian cancer growth in mice. Oncogene 37:4854-4870
Chiang, Cheryl Lai-Lai; Kandalaft, Lana E (2018) In vivo cancer vaccination: Which dendritic cells to target and how? Cancer Treat Rev 71:88-101
Hu, Xiaowen; Sood, Anil K; Dang, Chi V et al. (2018) The role of long noncoding RNAs in cancer: the dark matter matters. Curr Opin Genet Dev 48:8-15
Nacson, Joseph; Krais, John J; Bernhardy, Andrea J et al. (2018) BRCA1 Mutation-Specific Responses to 53BP1 Loss-Induced Homologous Recombination and PARP Inhibitor Resistance. Cell Rep 24:3513-3527.e7
Beck, Tim N; Smith, Chad H; Flieder, Douglas B et al. (2017) Head and neck squamous cell carcinoma: Ambiguous human papillomavirus status, elevated p16, and deleted retinoblastoma 1. Head Neck 39:E34-E39
Yang, Lu; Zhang, Youyou; Shan, Weiwei et al. (2017) Repression of BET activity sensitizes homologous recombination-proficient cancers to PARP inhibition. Sci Transl Med 9:
Skates, Steven J; Greene, Mark H; Buys, Saundra S et al. (2017) Early Detection of Ovarian Cancer using the Risk of Ovarian Cancer Algorithm with Frequent CA125 Testing in Women at Increased Familial Risk - Combined Results from Two Screening Trials. Clin Cancer Res 23:3628-3637
Zhang, Dongmei; Zhang, Gao; Hu, Xiaowen et al. (2017) Oncogenic RAS Regulates Long Noncoding RNA Orilnc1 in Human Cancer. Cancer Res 77:3745-3757
Prudnikova, Tatiana Y; Chernoff, Jonathan (2017) The Group I Pak inhibitor Frax-1036 sensitizes 11q13-amplified ovarian cancer cells to the cytotoxic effects of Rottlerin. Small GTPases 8:193-198

Showing the most recent 10 out of 323 publications