This revised application seeks renewal of the Chromosome Metabolism and Cancer Training Grant (CMCTG) at the Fred Hutchinson Cancer Research Center (Fred Hutch), an NCI-designated Comprehensive Cancer Center. The training program bridges the gap between basic and translational cancer research by bringing together young translational and basic scientists in one of the nation?s premier cancer research institutions, the Fred Hutchinson Cancer Research Center (Fred Hutch), and leverages the synergies emerging from an extraordinarily wide range of ongoing research. The CMCTG is the only Fred Hutch institutional training grant (T32) that is focused on molecular mechanisms of cancer. The 26 training faculty members include four junior faculty members who are being developed as the next generation of research mentors. Of the 22 senior trainers, four are members of the National Academy of Sciences and three are Howard Hughes Medical Institute Investigators. All of the training faculty have vigorous research programs and external funding, and most have support from the NCI, ACS, DoD or cancer foundations. The program is administered by the PI and Assistant PI and a Steering Committee comprising four of the training faculty plus the head of the Office of Scientific Career Development and an External Advisor. The goal of the program is to train young scientists toward a career in cancer research with special emphasis on investigating fundamental molecular and cell biology of normal and cancer cells. Our training program is based on the concept that the prevention, diagnosis, and treatment of cancer will require a profound understanding of the molecular mechanisms that underlie the behavior of normal cells and drive the initiation, progression, and maintenance of tumors and their environment. Training occurs in small, dedicated research labs on an integrated campus, allowing close monitoring of trainee progress, effective mentoring of junior members of the Training Faculty, and frequent exchange of ideas between trainees and mentors. Extensive core facilities support cutting-edge research. Over the past 10 years, the CMCTG has impacted the careers of 11 pre-doctoral and 35 postdoctoral trainees, of whom 2 predocs and 6 postdocs are still supported. 9 trainees are/were from under-represented minority groups. Of the 38 past trainees, 8 are junior faculty in research or teaching at universities, 8 are staff scientists or in science administration in academic settings, 5 have research positions in biotech, 14 remain in training at Fred Hutch or other institutions, 1 is deceased, 1 is on medical leave, and 1 is a homemaker. Seven postdoctoral trainees obtained independent research fellowships from the American Cancer Society, and four predoctoral trainees won prestigious NSF predoctoral fellowships. We plan to continue this record of success into the future.

Public Health Relevance

This revised renewal application seeks continuation of a long-standing training grant, The Chromosome Metabolism and Cancer Training Grant (CMCTG), that supports basic research into cancer at the Fred Hutchinson Cancer Research Center (Fred Hutch). The Fred Hutch provides a unique training environment in which the clinical, basic science, translational, and public health sciences division are in close proximity and highly focused on cancer. Research areas supported by the CMCTG include DNA replication, damage and repair, chromosome segregation and stability, epigenetics, protein structure, and the regulation of gene expression at multiple levels. Biological systems under study range from yeast to mice and patient samples; and include the generation and analysis of a wide range of neoplasms. Trainees employ these systems and cutting edge methods to study mechanisms of cell motility and metastasis, cancer immunology and genomics, tumor dormancy and microenvironment, and therapeutics and resistance. Moreover the program provides exposure to, and training in, technologies that are at the forefront of contemporary biology including proteomics, genomics, and advanced methods in microscopy and computational biology.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Institutional National Research Service Award (T32)
Project #
2T32CA009657-26A1
Application #
9209314
Study Section
Subcommittee F - Institutional Training and Education (NCI-F)
Program Officer
Lim, Susan E
Project Start
1991-04-01
Project End
2021-08-31
Budget Start
2016-09-15
Budget End
2017-08-31
Support Year
26
Fiscal Year
2016
Total Cost
$390,340
Indirect Cost
$32,868
Name
Fred Hutchinson Cancer Research Center
Department
Type
DUNS #
078200995
City
Seattle
State
WA
Country
United States
Zip Code
98109
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
Campbell, Amy E; Shadle, Sean C; Jagannathan, Sujatha et al. (2018) NuRD and CAF-1-mediated silencing of the D4Z4 array is modulated by DUX4-induced MBD3L proteins. Elife 7:
Cimino, Patrick J; Kim, Youngmi; Wu, Hua-Jun et al. (2018) Increased HOXA5 expression provides a selective advantage for gain of whole chromosome 7 in IDH wild-type glioblastoma. Genes Dev 32:512-523
Blair, Kris M; Mears, Kevin S; Taylor, Jennifer A et al. (2018) The Helicobacter pylori cell shape promoting protein Csd5 interacts with the cell wall, MurF, and the bacterial cytoskeleton. Mol Microbiol 110:114-127
Nyquist, Michael D; Corella, Alexandra; Burns, John et al. (2017) Exploiting AR-Regulated Drug Transport to Induce Sensitivity to the Survivin Inhibitor YM155. Mol Cancer Res 15:521-531
Pattwell, Siobhan S; Bath, Kevin G (2017) Emotional learning, stress, and development: An ever-changing landscape shaped by early-life experience. Neurobiol Learn Mem 143:36-48
Anderson, Kristin G; Stromnes, Ingunn M; Greenberg, Philip D (2017) Obstacles Posed by the Tumor Microenvironment to T cell Activity: A Case for Synergistic Therapies. Cancer Cell 31:311-325
Pattwell, Siobhan S; Holland, Eric C (2017) Putting Glioblastoma in Its Place: IRF3 Inhibits Invasion. Trends Mol Med 23:773-776
Deyter, Gary M R; Hildebrand, Erica M; Barber, Adrienne D et al. (2017) Histone H4 Facilitates the Proteolysis of the Budding Yeast CENP-ACse4 Centromeric Histone Variant. Genetics 205:113-124
Campbell, Amy E; Oliva, Jonathan; Yates, Matthew P et al. (2017) BET bromodomain inhibitors and agonists of the beta-2 adrenergic receptor identified in screens for compounds that inhibit DUX4 expression in FSHD muscle cells. Skelet Muscle 7:16

Showing the most recent 10 out of 113 publications