Cancer Basic Biology Program The Cancer Basic Biology Program (CBB) aims to understand the fundamental genomic and cellular mechanisms that regulate the normal and transformed phenotype; to develop new molecular approaches and tools to advance cancer diagnosis and therapy; and to develop with other Consortium programs the intellectual and technical infrastructure to advance translational cancer research. There are three major scientific themes: 1. The biology of the nucleus in normal and tumor cells, with a focus on mechanisms regulating altered gene expression and the loss of genome stability in cancer; 2. Regulation of normal and cancer cell phenotypes including the regulation of the cell cycle and motility, and the use of genetic, metabolic and high-throughput screening strategies to improve cancer diagnosis and therapy; and 3. Protein design and genome engineering as enabling technologies to advance basic and translational cancer biology. The CCSG supports this research program by providing key shared resources, particularly Genomics, Proteomics, Cellular Imaging and Comparative Medicine; administrative support for meetings, clubs and interest groups; and pilot funding and new investigator funds. The Cancer Basic Biology Program currently has 73 members from 18 departments and 2 Institutions. 42 members have primary appointments at FHCRC and 31 at UW. 68 Members (93%) have peer-reviewed funding or are newly recruited and supported by their institution. The Cancer Basic Biology Program currently has $32.6M in peer-reviewed funding (direct) $7.1 of which (21%) is from NCI. Due to the tradition of basic research in small independent laboratories, most support is in the form of R01s. The Cancer Basic Biology Program published a total of 1116 papers in the previous grant period: 12% were intra-programmatic, 17% were inter-programmatic, and 11% were inter-institutional.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA015704-44
Application #
9617722
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2019-01-01
Budget End
2019-12-31
Support Year
44
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Fred Hutchinson Cancer Research Center
Department
Type
DUNS #
078200995
City
Seattle
State
WA
Country
United States
Zip Code
98109
Birnbaum, Jeanette K; Duggan, Catherine; Anderson, Benjamin O et al. (2018) Early detection and treatment strategies for breast cancer in low-income and upper middle-income countries: a modelling study. Lancet Glob Health 6:e885-e893
Herman, Daniel S; Smith, Christina; Liu, Chang et al. (2018) Efficient Detection of Copy Number Mutations in PMS2 Exons with a Close Homolog. J Mol Diagn 20:512-521
Jia, Deshui; Augert, Arnaud; Kim, Dong-Wook et al. (2018) Crebbp Loss Drives Small Cell Lung Cancer and Increases Sensitivity to HDAC Inhibition. Cancer Discov 8:1422-1437
Partridge, Emma K; Neuhouser, Marian L; Breymeyer, Kara et al. (2018) Comparison of Nutrient Estimates Based on Food Volume versus Weight: Implications for Dietary Assessment Methods. Nutrients 10:
Neumeyer, Sonja; Banbury, Barbara L; Arndt, Volker et al. (2018) Mendelian randomisation study of age at menarche and age at menopause and the risk of colorectal cancer. Br J Cancer 118:1639-1647
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Yu, Hsiang; Cheng, Yu-Jen; Wang, Ching-Yun (2018) Methods for multivariate recurrent event data with measurement error and informative censoring. Biometrics 74:966-976
Puré, Ellen; Hingorani, Sunil R (2018) Mesenchymal Cell Plasticity and Perfidy in Epithelial Malignancy. Trends Cancer 4:273-277
Barault, Ludovic; Amatu, Alessio; Siravegna, Giulia et al. (2018) Discovery of methylated circulating DNA biomarkers for comprehensive non-invasive monitoring of treatment response in metastatic colorectal cancer. Gut 67:1995-2005
Linden, Hannah M; Peterson, Lanell M; Fowler, Amy M (2018) Clinical Potential of Estrogen and Progesterone Receptor Imaging. PET Clin 13:415-422

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