The molecular basis of all cancers is the accumulation of heritable genetic and epigenetic changes that result in loss of function of tumor suppressors and/or the inappropriate activation of proto-oncogenes. At the time of the last review, UVa and the Cancer Center had several investigators among its ranks who worked on various aspects of gene expression, replication, and genetic instability. However, a need was appreciated for a stronger representation of such programs within the Cancer Center and for a formal mechanism to foster intellectual exchange and collaborations. The Molecular Genetics Program was initiated to facilitate the focused, interactive, study of chromatin architecture, transcription, replication, mutation, repair, and cellular checkpoints. The long-range goals of this group are to understand the molecular mechanisms that underlie genetic and epigenetic defects in cancer. This new Program currently consists of 24 active investigators from 7 different departments, 13 of whom derived from other Programs in the Center and 11 of whom were recruited to UVa since the last renewal. Total extramural funding for the Molecular Genetics Program exceeds $9 million, including $2.6 million from the NCI and $550K from ACS or cancer-targeted DOD awards. This diverse but cohesive group meets monthly to hear presentations by its own members or by investigators in other relevant Programs. In the last two years, this monthly forum has also hosted four mini-symposia focused on particular cancers. A research retreat off-site provides a venue for short platform talks and posters, thus keeping the group abreast of the research progress of the other members of the Molecular Genetics Program in a comprehensive way on a yearly basis. The group's members have also organized six symposia hosting outside speakers on topics relevant to cancer genetics and epigenetics. These activities have stimulated creative and informed thinking on the cancer problem, and have provided the framework for many productive collaborations among Cancer Center members. The goals of the Program are to develop comprehensive molecular models for the origins of genetic and epigenetic instability in cancer and to help uncover novel genes responsible for the development of neoplasms in diverse tumor types. In the short history of this Program, it has fostered several studies leading to the identification of therapeutic targets and more rational approaches to cancer therapy. The many activities and interactions have led directly or indirectly to 343 publications, of which 31% were inter-programmatic publications and 9% were intra-programmatic publications since the last renewal. In addition, Program members participate in 12 multi-investigator or collaborative NIH research awards including 8 from the NCI.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA044579-18
Application #
7726776
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2008-02-01
Budget End
2009-01-31
Support Year
18
Fiscal Year
2008
Total Cost
$14,755
Indirect Cost
Name
University of Virginia
Department
Type
DUNS #
065391526
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
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Olson, Kristine C; Kulling Larkin, Paige M; Signorelli, Rossana et al. (2018) Vitamin D pathway activation selectively deactivates signal transducer and activator of transcription (STAT) proteins and inflammatory cytokine production in natural killer leukemic large granular lymphocytes. Cytokine 111:551-562
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Carhart, Miev Y; Schminkey, Donna L; Mitchell, Emma M et al. (2018) Barriers and Facilitators to Improving Virginia's HPV Vaccination Rate: A Stakeholder Analysis With Implications for Pediatric Nurses. J Pediatr Nurs 42:1-8
Hao, Yi; Bjerke, Glen A; Pietrzak, Karolina et al. (2018) TGF? signaling limits lineage plasticity in prostate cancer. PLoS Genet 14:e1007409
Obeid, Joseph M; Kunk, Paul R; Zaydfudim, Victor M et al. (2018) Immunotherapy for hepatocellular carcinoma patients: is it ready for prime time? Cancer Immunol Immunother 67:161-174
Wallrabe, Horst; Svindrych, Zdenek; Alam, Shagufta R et al. (2018) Segmented cell analyses to measure redox states of autofluorescent NAD(P)H, FAD & Trp in cancer cells by FLIM. Sci Rep 8:79
Olmez, Inan; Love, Shawn; Xiao, Aizhen et al. (2018) Targeting the mesenchymal subtype in glioblastoma and other cancers via inhibition of diacylglycerol kinase alpha. Neuro Oncol 20:192-202
Wang, T Tiffany; Yang, Jun; Zhang, Yong et al. (2018) IL-2 and IL-15 blockade by BNZ-1, an inhibitor of selective ?-chain cytokines, decreases leukemic T-cell viability. Leukemia :
Yao, Nengliang; Zhu, Xi; Dow, Alan et al. (2018) An exploratory study of networks constructed using access data from an electronic health record. J Interprof Care :1-8

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