The Developmental Therapeutics Research Program (DTP) is a long-standing interdisciplinary research program that was established in 1974, and this program was the first research program of the Yale Cancer Center (YCC). This program has 36 members representing 13 academic departments of the School of Medicine and 2 schools of Yale University. The leaders of the Program are Yung-Chi Cheng, Ph.D. and Edward Chu, M.D., who are leading experts in the field of developmental therapeutics and cancer drug development. They recruit, develop, and provide guidance to investigators interested in cancer pharmacology and developmental therapeutics. They foster and facilitate inter- and intra-programmatic collaborations and identify ways in which the membership of this research program can benefit from the shared resources of the YCC. The major focus of the Program is in the area of cancer and viral (those associated with cancer or those playing an important role in the etiology of cancer) chemotherapy. Specifically, the Program focuses on the following major areas of investigation: (1) target identification, validation, and characterization;(2) characterization of the molecular/biochemical pharmacology of anticancer and antiviral compounds and characterization of the mechanisms of cellular drug resistance;(3) drug discovery/development;and (4) clinical trial design and development. Members are selected based on their scientific credentials, which must focus on basic, translational, and clinical cancer research. A high priority is placed on members who are deeply committed to the goals set forth by the Program and who focus on developing extensive intra-programmatic interactions as well as strong interactions/collaborations with other YCC research programs. In particular, significant efforts have been placed on developing a strong translational clinical program of developing novel anticancer agents and new combination regimens for the treatment of human cancers. Finally, the membership of the Developmental Therapeutics Program is actively encouraged to make extensive use of the YCC shared resources. Total peer-reviewed funding support of this group is approximately $5.7 million direct costs annually ($8.7 million total costs), of which $2.89 million direct costs ($4.49 million total costs) is from the National Cancer Institute (NCI). In addition, nearly a $2.3 million direct cost ($2.8 total costs) is received annually from nonpeer reviewed granting mechanisms. During the previous grant period, members of this program published 697 cancer-related papers, of which 10% were intra-programmatic and 12% inter-programmatic.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016359-32
Application #
8132519
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2010-08-01
Budget End
2011-07-31
Support Year
32
Fiscal Year
2010
Total Cost
$33,424
Indirect Cost
Name
Yale University
Department
Type
DUNS #
043207562
City
New Haven
State
CT
Country
United States
Zip Code
06520
Jagannath, Sundar; Laubach, Jacob; Wong, Ellice et al. (2018) Elotuzumab monotherapy in patients with smouldering multiple myeloma: a phase 2 study. Br J Haematol 182:495-503
Liu, Xiaoni; Zhang, Shang-Min; McGeary, Meaghan K et al. (2018) KDM5B Promotes Drug Resistance by Regulating Melanoma Propagating Cell Subpopulations. Mol Cancer Ther :
Chae, Wook-Jin; Bothwell, Alfred L M (2018) Therapeutic Potential of Gene-Modified Regulatory T Cells: From Bench to Bedside. Front Immunol 9:303
Kim, Hanseul; Keum, NaNa; Giovannucci, Edward L et al. (2018) Garlic intake and gastric cancer risk: Results from two large prospective US cohort studies. Int J Cancer 143:1047-1053
Sarma, Elizabeth A; Kawachi, Ichiro; Poole, Elizabeth M et al. (2018) Social integration and survival after diagnosis of colorectal cancer. Cancer 124:833-840
Hartman, Douglas J; Ahmad, Fahad; Ferris, Robert L et al. (2018) Utility of CD8 score by automated quantitative image analysis in head and neck squamous cell carcinoma. Oral Oncol 86:278-287
Chen, Ling; Azuma, Takeshi; Yu, Weiwei et al. (2018) B7-H1 maintains the polyclonal T cell response by protecting dendritic cells from cytotoxic T lymphocyte destruction. Proc Natl Acad Sci U S A 115:3126-3131
Zhang, Jinhua; Song, Kun; Wang, Jun et al. (2018) S100A4 blockage alleviates agonistic anti-CD137 antibody-induced liver pathology without disruption of antitumor immunity. Oncoimmunology 7:e1296996
Kelada, Olivia J; Decker, Roy H; Nath, Sameer K et al. (2018) High Single Doses of Radiation May Induce Elevated Levels of Hypoxia in Early-Stage Non-Small Cell Lung Cancer Tumors. Int J Radiat Oncol Biol Phys 102:174-183
Powles, Ryan L; Redmond, David; Sotiriou, Christos et al. (2018) Association of T-Cell Receptor Repertoire Use With Response to Combined Trastuzumab-Lapatinib Treatment of HER2-Positive Breast Cancer: Secondary Analysis of the NeoALTTO Randomized Clinical Trial. JAMA Oncol 4:e181564

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