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
Sanmamed, Miguel F; Chen, Lieping (2018) A Paradigm Shift in Cancer Immunotherapy: From Enhancement to Normalization. Cell 175:313-326
Gupta, Swati; Mani, Navin R; Carvajal-Hausdorf, Daniel E et al. (2018) Macrodissection prior to closed system RT-qPCR is not necessary for estrogen receptor and HER2 concordance with IHC/FISH in breast cancer. Lab Invest 98:1076-1083
Bellone, Stefania; Buza, Natalia; Choi, Jungmin et al. (2018) Exceptional Response to Pembrolizumab in a Metastatic, Chemotherapy/Radiation-Resistant Ovarian Cancer Patient Harboring a PD-L1-Genetic Rearrangement. Clin Cancer Res 24:3282-3291
Altan, Mehmet; Kidwell, Kelley M; Pelekanou, Vasiliki et al. (2018) Association of B7-H4, PD-L1, and tumor infiltrating lymphocytes with outcomes in breast cancer. NPJ Breast Cancer 4:40
Kim, Tae Kon; Herbst, Roy S; Chen, Lieping (2018) Defining and Understanding Adaptive Resistance in Cancer Immunotherapy. Trends Immunol 39:624-631
Goldberg, Sarah B; Patel, Abhijit A (2018) Monitoring immunotherapy outcomes with circulating tumor DNA. Immunotherapy 10:1023-1025
Wang, Shi-Yi; Long, Jessica B; Killelea, Brigid K et al. (2018) Associations of preoperative breast magnetic resonance imaging with subsequent mastectomy and breast cancer mortality. Breast Cancer Res Treat 172:453-461
Bonazzoli, Elena; Predolini, Federica; Cocco, Emiliano et al. (2018) Inhibition of BET Bromodomain Proteins with GS-5829 and GS-626510 in Uterine Serous Carcinoma, a Biologically Aggressive Variant of Endometrial Cancer. Clin Cancer Res 24:4845-4853
Villarroel-Espindola, Franz; Yu, Xiaoqing; Datar, Ila et al. (2018) Spatially Resolved and Quantitative Analysis of VISTA/PD-1H as a Novel Immunotherapy Target in Human Non-Small Cell Lung Cancer. Clin Cancer Res 24:1562-1573
Wadia, Roxanne J; Stolar, Marilyn; Grens, Clarice et al. (2018) The prevention of chemotherapy induced peripheral neuropathy by concurrent treatment with drugs used for bipolar disease: a retrospective chart analysis in human cancer patients. Oncotarget 9:7322-7331

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