Harold C. Simmons Cancer Center Experimental Therapeutics of Cancer Scientific Program Project Summary/Abstract The Experimental Therapeutics (ET) Program brings together 44 full Simmons Cancer Center (SCC) members, including 13 from basic science departments and 31 from clinical departments, to develop novel therapeutic strategies and to evaluate these approaches by conducting investigator-initiated clinical trials. The program has 27 NCI projects, a lung cancer SPORE, as well as 12 multi-investigator awards. ET Program clinical investigators represent key oncology disciplines, including medical, surgical, pediatrics, and radiation oncology; radiology; and pathology. Investigators in the ET Program are currently supported by over $24.7 million in peer-reviewed funding (total costs) with $7.5 million from the NCI, $4 million from other NIH sources, and $7.3 million from the Cancer Prevention and Research Institute of Texas (CPRIT) The ET Program is designed to provide an organized, science-based conduit for translating SCC discoveries from the scientific programs to the clinic, and to help establish appropriate preclinical models and data to facilitate clinical translation. Likewise, clinical data are then used to form new hypotheses tested by our strong basic science foundation throughout the SCC. The program themes focus on drug (Themes 1,2) and biomarker (Themes 3,4) discovery to identify optimal populations for these new treatments. Theme 1: Molecular Therapeutic Sensitizers Theme 2: Tumor Microenvironment and Protein Therapy Theme 3: Imaging and Drug Delivery Theme 4: Cancer Vulnerabilities The Co-Leaders of the ET Program work together to foster and develop themes, goals, membership, and new collaborations in specific research areas for clinical translation. This process heavily engages SCC disease DOTs (disease oriented teams) to focus specific therapeutics on select cancers, as evidenced by mechanistic- based research where target validation is assessed using pharmacodynamic biomarkers. These activities, in turn, stimulate intra- and inter-programmatic collaborations. The ET Program averages over 100 publications per year, and since 2009 the level of collaborative publications has remained quite high, with 35% intra- programmatic, 34% inter-programmatic and 28% inter-institutional with authors in other NCI-designated cancer centers.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
3P30CA142543-10S3
Application #
10260733
Study Section
Subcommittee I - Transistion to Independence (NCI)
Program Officer
Belin, Precilla L
Project Start
2010-08-03
Project End
2021-07-31
Budget Start
2019-08-01
Budget End
2020-07-31
Support Year
10
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Type
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390
O'Kelly, Devin; Zhou, Heling; Mason, Ralph P (2018) Tomographic breathing detection: a method to noninvasively assess in situ respiratory dynamics. J Biomed Opt 23:1-6
Chen, Yan; Zhang, Bo; Bao, Lei et al. (2018) ZMYND8 acetylation mediates HIF-dependent breast cancer progression and metastasis. J Clin Invest 128:1937-1955
Stallings, Nancy R; O'Neal, Melissa A; Hu, Jie et al. (2018) Pin1 mediates A?42-induced dendritic spine loss. Sci Signal 11:
Sudhan, Dhivya R; Schwarz, Luis J; Guerrero-Zotano, Angel et al. (2018) Extended Adjuvant Therapy with Neratinib Plus Fulvestrant Blocks ER/HER2 Crosstalk and Maintains Complete Responses of ER+/HER2+ Breast Cancers: Implications to the ExteNET Trial. Clin Cancer Res :
Pruitt, Sandi L; Werner, Claudia L; Borton, Eric K et al. (2018) Cervical Cancer Burden and Opportunities for Prevention in a Safety-Net Healthcare System. Cancer Epidemiol Biomarkers Prev 27:1398-1406
Shay, Laura A; Baldwin, Austin S; Betts, Andrea C et al. (2018) Parent-Provider Communication of HPV Vaccine Hesitancy. Pediatrics 141:
Murphy, Caitlin C; Sigel, Bianca M; Yang, Edward et al. (2018) Adherence to colorectal cancer screening measured as the proportion of time covered. Gastrointest Endosc 88:323-331.e2
Taylor 4th, Clinton A; An, Sung-Wan; Kankanamalage, Sachith Gallolu et al. (2018) OSR1 regulates a subset of inward rectifier potassium channels via a binding motif variant. Proc Natl Acad Sci U S A 115:3840-3845
Deng, Mi; Gui, Xun; Kim, Jaehyup et al. (2018) LILRB4 signalling in leukaemia cells mediates T cell suppression and tumour infiltration. Nature 562:605-609
Lee, Simon Craddock; Higashi, Robin T; Sanders, Joanne M et al. (2018) Effects of program scale-up on time to resolution for patients with abnormal screening mammography results. Cancer Causes Control 29:995-1005

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