This application is a renewal request for funding of the Training Program in Oncogenesis and Developmental Biology (T32 CA080621) at the Robert H. Lurie Comprehensive Cancer Center of Northwestern University. Over the past 10 years, this Training Program has been preparing pre-doctoral students and post-doctoral trainees to work at the interface between cancer and developmental biology through laboratory research, formal course work and participation in seminars, journal clubs and group meetings. The hypothesis of this Training Program is that an understanding of key processes in developmental biology informs studies of oncogenesis. Trainees will use their understanding of normal development to identify lesions that are functionally significant for oncogenic transformation. The intent is to train a cohort of investigators who ultimately use this informatio for therapeutically targeting the cancer stem cell. In the first ten years of funding, the Training Program in Oncogenesis and Developmental Biology effectively trained 15 pre-doctoral students and 23 post-doctoral fellows; 14 remain in training. Of the trainees who have completed the Training Program, 9 have obtained faculty appointments, 9 have obtained relevant positions in industry, and over 25% have successfully competed for national funding. In this renewal application, we propose expansion of the Training Program to include a required career development curriculum and multi-disciplinary training in cutting edge technologies that are relevant to cancer research. We also further define the required and recommended courses in cancer and developmental biology that are specific to the trainee level. To facilitate identification and support of the highest quality of trainees, we have expanded the Northwestern University based selection and evaluation committee. We have also added an External Advisory Committee that includes individuals with involvement in high caliber T32 programs to further assist us in achieving this goal. In the current renewal application, we request funding for two pre-doctoral students and four post- doctoral fellows per year for a period of five years. This wil enable us to continue focused training in Oncogenesis and Developmental Biology.

Public Health Relevance

This Program trains graduate students and postdoctoral fellows at the interface of oncogenesis and developmental biology and prepares them for careers as independent scientists. A group of highly qualified faculty at Northwestern University who work in various areas of developmental and cancer have been assembled to provide scientific oversight and mentorship to our trainees.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Institutional National Research Service Award (T32)
Project #
5T32CA080621-14
Application #
9331423
Study Section
Subcommittee I - Transistion to Independence (NCI)
Program Officer
Perkins, Susan N
Project Start
2001-04-06
Project End
2019-08-31
Budget Start
2017-09-01
Budget End
2018-08-31
Support Year
14
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Northwestern University at Chicago
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
005436803
City
Chicago
State
IL
Country
United States
Zip Code
60611
Pituch, Katarzyna C; Miska, Jason; Krenciute, Giedre et al. (2018) Adoptive Transfer of IL13R?2-Specific Chimeric Antigen Receptor T Cells Creates a Pro-inflammatory Environment in Glioblastoma. Mol Ther 26:986-995
Goretsky, Tatiana; Bradford, Emily M; Ye, Qing et al. (2018) Beta-catenin cleavage enhances transcriptional activation. Sci Rep 8:671
Suraneni, Praveen K; Corey, Seth J; Hession, Michael J et al. (2018) Dynamins 2 and 3 control the migration of human megakaryocytes by regulating CXCR4 surface expression and ITGB1 activity. Blood Adv 2:3540-3552
Volk, Andrew; Liang, Kaiwei; Suraneni, Praveen et al. (2018) A CHAF1B-Dependent Molecular Switch in Hematopoiesis and Leukemia Pathogenesis. Cancer Cell 34:707-723.e7
Miska, Jason; Lui, Jen Bon; Toomer, Kevin H et al. (2018) Initiation of inflammatory tumorigenesis by CTLA4 insufficiency due to type 2 cytokines. J Exp Med 215:841-858
Smith, Erica D; Garza-Gongora, Arturo G; MacQuarrie, Kyle L et al. (2018) Interstitial telomeric loops and implications of the interaction between TRF2 and lamin A/C. Differentiation 102:19-26
Chen, Jessie; Van Gulden, Stephanie; McGuire, Tammy L et al. (2018) BMP-Responsive Protease HtrA1 Is Differentially Expressed in Astrocytes and Regulates Astrocytic Development and Injury Response. J Neurosci 38:3840-3857
Arslan, A D; Sassano, A; Saleiro, D et al. (2017) Human SLFN5 is a transcriptional co-repressor of STAT1-mediated interferon responses and promotes the malignant phenotype in glioblastoma. Oncogene 36:6006-6019
Qadir, Abdul S; Ceppi, Paolo; Brockway, Sonia et al. (2017) CD95/Fas Increases Stemness in Cancer Cells by Inducing a STAT1-Dependent Type I Interferon Response. Cell Rep 18:2373-2386
Bradford, Emily M; Ryu, Stacy H; Singh, Ajay Pal et al. (2017) Epithelial TNF Receptor Signaling Promotes Mucosal Repair in Inflammatory Bowel Disease. J Immunol 199:1886-1897

Showing the most recent 10 out of 83 publications