This proposal requests renewal of support for a postdoctoral training program, now in its 28th year, at the NCI designated Basic Cancer Center of the Salk Institute for Biological Studies. This program provides advanced training in research to postdoctoral scientists pursuing careers in basic and translational research related to cancer. Major activities include molecular, cell and developmental biology research within the three Cancer Center Programs: Metabolism and Cancer, Mouse Models and Cancer Stem Cells, and Growth Control and Genomic Stability. The Cancer Center occupies 73,000 sq. ft. of laboratory space and includes 32 faculty members, 22 of whom are members of the training faculty. Currently there are 187 postdoctoral and 58 predoctoral trainees in the Cancer Center. Trainees devote 100% of their time to research. Trainees in the program also participate in a variety of special activities designed to enhance their knowledge of cancer biology and therapeutic applications of basic research. These include the Cancer Biology Course, Cancer Forum and Cancer Center Symposium. These activities are designed to significantly augment the cancer relevance and focus of the individual laboratory training experience. We request funding to continue to support six trainees. The trainees will hold Ph.D. and/or M.D. degrees, and will be chosen on the basis of the quality and cancer relevance of research proposals they submit. The average duration of training will be three years, as at present. Upon completion of training the trainees will be fully qualified to conduct independent research in molecular and cellular biology related to cancer.

Public Health Relevance

The Cancer Center of the Salk Institute for Biological Studies provides a rich environment for postdoctoral research training for qualified candidates with the Ph.D. and/or M.D. degrees. Trainees are prepared for careers as independent research investigators through firsthand experience designing and performing cutting edge research in basic and translational studies in cancer biology. The Cancer Center Training Program also provides courses, seminars, and a forum for research discussions to enhance this training experience. The written critiques and criteria scores of individual reviewers are provided in essentially unedited form in the Critique section below. Please note that these critiques and criteria scores were prepared prior to the meeting and may not have been revised subsequent to any discussions at the review meeting. The Resume and Summary of Discussion above summarizes the final opinions of the committee.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Institutional National Research Service Award (T32)
Project #
5T32CA009370-31
Application #
8320880
Study Section
Special Emphasis Panel (ZCA1-RTRB-K (M1))
Program Officer
Lim, Susan E
Project Start
1980-09-01
Project End
2016-08-31
Budget Start
2012-09-01
Budget End
2013-08-31
Support Year
31
Fiscal Year
2012
Total Cost
$375,769
Indirect Cost
$28,134
Name
Salk Institute for Biological Studies
Department
Type
DUNS #
078731668
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Gatchalian, Jovylyn; Malik, Shivani; Ho, Josephine et al. (2018) A non-canonical BRD9-containing BAF chromatin remodeling complex regulates naive pluripotency in mouse embryonic stem cells. Nat Commun 9:5139
Eichner, Lillian J; Brun, Sonja N; Herzig, Sébastien et al. (2018) Genetic Analysis Reveals AMPK Is Required to Support Tumor Growth in Murine Kras-Dependent Lung Cancer Models. Cell Metab :
McFall, Thomas; McKnight, Brooke; Rosati, Rayna et al. (2018) Progesterone receptor A promotes invasiveness and metastasis of luminal breast cancer by suppressing regulation of critical microRNAs by estrogen. J Biol Chem 293:1163-1177
Xia, Yifeng; Zhan, Cheng; Feng, Mingxiang et al. (2018) Targeting CREB Pathway Suppresses Small Cell Lung Cancer. Mol Cancer Res 16:825-832
Katz, Zachary B; Novotná, Lucie; Blount, Amy et al. (2017) A cycle of Zap70 kinase activation and release from the TCR amplifies and disperses antigenic stimuli. Nat Immunol 18:86-95
Fuhs, Stephen Rush; Hunter, Tony (2017) pHisphorylation: the emergence of histidine phosphorylation as a reversible regulatory modification. Curr Opin Cell Biol 45:8-16
Saison-Ridinger, Maya; DelGiorno, Kathleen E; Zhang, Tejia et al. (2017) Reprogramming pancreatic stellate cells via p53 activation: A putative target for pancreatic cancer therapy. PLoS One 12:e0189051
Gibson, Matthew D; Gatchalian, Jovylyn; Slater, Andrew et al. (2017) PHF1 Tudor and N-terminal domains synergistically target partially unwrapped nucleosomes to increase DNA accessibility. Nucleic Acids Res 45:3767-3776
Tencer, Adam H; Cox, Khan L; Di, Luo et al. (2017) Covalent Modifications of Histone H3K9 Promote Binding of CHD3. Cell Rep 21:455-466
Tencer, Adam H; Gatchalian, Jovylyn; Klein, Brianna J et al. (2017) A Unique pH-Dependent Recognition of Methylated Histone H3K4 by PPS and DIDO. Structure 25:1530-1539.e3

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