The Cancer Genetics and Genomics Program (CGG) consists of 44 independent but interactive members belonging to 14 departments with common interests in the cancer genome and its genes. Under the leadership of Drs. Lajos Pusztai and Frank Slack, the CGG promotes: (1) research into the role of specific normal and mutant genes and biochemical pathways involving products of those genes in human cancer, including identifying and characterizing novel somatic and hereditary cancer genes using whole genome approaches such as resequencing and mouse knock out technologies;(2) research into mechanisms of gene regulation, including epigenetic processes that control gene expression, particularly as it pertains to human cancer, including incorporating the global, genome-wide study of genome structure, gene transcription, and protein synthesis;(3) research into the development of techniques and approaches that further the first 2 goals and, in particular, applying novel research findings to cancer risk assessment, diagnosis, therapy and rational drug development. CGG collaborates extensively with the Cancer Prevention &Control Program (CPC) and the Developmental Therapeutics Program (DT). The goals of CGG are accomplished through a monthly group meeting, administration of a Pilot Grant program to stimulate programmatically-oriented research in cancer, and by facilitating collaboration between members within the program and other Cancer Center programs. The CGG is derived from the former Cancer Genetics Program (CG) and the Gene Regulation and Functional Genomics (GRFG) Program and was renamed to reflect the overlap and strength in the two former programs. In aggregate, the program membership was altered to increase cancer focus as well as to add several outstanding new members. The reorganization reflects the profound developments that have occurred in the molecular genetics of cancer, as well as in the broader field of genomics. An increased emphasis on translational research is evident from the co-leadership of a basic and a clinical researcher, as well as a number of important collaborative grants such as the Skin Cancer SPORE, a lung cancer SPORE submission and the Yale-Gile'ad Collaboration. Total peer-reviewed funding is $5.6M direct costs annually (S8.9M total costs), of which $1.9M direct costs ($3.2M total costs) come from NCI. Total direct funding is $8.2M ($12.3M total costs). During the previous grant period, CGG members published 475 cancer-related papers, of which 17% were intra-programmatic and 35% inter-programmatic, and members have received $1,075,000 in YCC pilot funds and leveraged that into >$5.8M in extramural funding.

Public Health Relevance

CGG is made up of collaborative, cancer-focused scientists with interests in the cancer genome and its genes. The program combines the strengths of a highly productive basic science faculty in discovering fundamental mechanisms of cancer biology with the expertise of a growing clinical science faculty to translate these discoveries into therapeutic and diagnostic advances in the clinic. The program is knitted together with a monthly research seminar, leading to substantial intra- and interprogrammatic collaborations

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016359-35
Application #
8755628
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2014-08-01
Budget End
2015-07-31
Support Year
35
Fiscal Year
2014
Total Cost
$19,834
Indirect Cost
$7,922
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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