The overall goal of the Moffitt Cancer Center (MCC) Chemical Biology and Molecular Medicine (CBMM) Program is to integrate chemical biology and systems biology technologies to develop new therapeutic approaches for the treatment of cancer. The CBMM Program evolved through a strategic merging of the prior Experimental Therapeutics (ET) Program and the drug discovery activities of the Molecular Oncology and Drug Discovery (MODD) Program. This addressed an overlap noted at the prior review and the change was endorsed by MCC's EAC and the NCI. The realignment allows for focused activity in specific areas of excellence within CBMM and better aligns members with focused aims. Along with research in chemistry and drug discovery and clinical trials, the CBMM now includes members interrogating signaling pathways that regulate cell proliferation and survival to identify new targets for cancer therapeutics. Inclusion of basic scientists, chemists, and clinical researchers creates unique opportunities to rapidly translate novel strategies into the clinic, while conversely also increasing the flow of observations from the clinic back to the laboratory for mechanistic testing. To better capture cancer signaling events and opportunities for drug discovery, a major area of growth within CBMM has been target discovery using system-level unbiased mass spectrometry-based proteomics. This strategy has successfully defined mechanisms of acquired resistance in refractory cancers as well as new therapeutic strategies for treating patients. Further, drug discovery science has evolved to enable design of not only single but also dual-targeting small molecule therapeutics using novel chemical probes, solving drug-target structures with x-ray crystallography and structure-based drug design. Tumor profiling technologies, including genomics, proteomics, and imaging, are being fully used for targeted agent clinical trials, defining small molecule mechanisms of action, refining prognostic and predictive markers, and studying the process of drug resistance. As a consequence of these changes, CBMM membership has been consolidated from 57 (30 Scientific, 27 Clinical Trialists) to 43 members (21 Scientific, 22 Clinical Trialists) including 10 new basic science and 15 clinical investigators. CBMM has been successful in obtaining $17.9M in total annual funding, including $10.8M in industry-supported clinical trials, $6.0M in NCI funding, and $0.9M in other peer-reviewed funding. During the current funding period, members published 915 articles, with 318 (35%) of these publications representing intra-programmatic collaborations, 320 (35%) inter-programmatic, and 334 (37%) representing inter-institutional publications with other NCI-designated Cancer Centers. The Program accrued 3,995 patients to interventional clinical trials, including 3,897 to treatment intervention trials.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA076292-21
Application #
9637362
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2019-02-01
Budget End
2020-01-31
Support Year
21
Fiscal Year
2019
Total Cost
Indirect Cost
Name
H. Lee Moffitt Cancer Center & Research Institute
Department
Type
DUNS #
139301956
City
Tampa
State
FL
Country
United States
Zip Code
33612
Kahen, Elliot John; Brohl, Andrew; Yu, Diana et al. (2018) Neurofibromin level directs RAS pathway signaling and mediates sensitivity to targeted agents in malignant peripheral nerve sheath tumors. Oncotarget 9:22571-22585
Hoffman, Melissa A; Fang, Bin; Haura, Eric B et al. (2018) Comparison of Quantitative Mass Spectrometry Platforms for Monitoring Kinase ATP Probe Uptake in Lung Cancer. J Proteome Res 17:63-75
Puri, Sonam; Hyland, Kelly A; Weiss, Kristine Crowe et al. (2018) Prediction of chemotherapy-induced nausea and vomiting from patient-reported and genetic risk factors. Support Care Cancer 26:2911-2918
Gonzalez, Brian D; Small, Brent J; Cases, Mallory G et al. (2018) Sleep disturbance in men receiving androgen deprivation therapy for prostate cancer: The role of hot flashes and nocturia. Cancer 124:499-506
Eroglu, Zeynep; Zaretsky, Jesse M; Hu-Lieskovan, Siwen et al. (2018) High response rate to PD-1 blockade in desmoplastic melanomas. Nature 553:347-350
Lu, Yingchang; Beeghly-Fadiel, Alicia; Wu, Lang et al. (2018) A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk. Cancer Res 78:5419-5430
Phadke, Manali; Remsing Rix, Lily L; Smalley, Inna et al. (2018) Dabrafenib inhibits the growth of BRAF-WT cancers through CDK16 and NEK9 inhibition. Mol Oncol 12:74-88
Kasting, Monica L; Christy, Shannon M; Sutton, Steven K et al. (2018) Florida physicians' reported use of AFIX-based strategies for human papillomavirus vaccination. Prev Med 116:143-149
Jiang, Kun; Neill, Kevin; Cowden, Daniel et al. (2018) Expression of CAS/CSE1L, the Cellular Apoptosis Susceptibility Protein, Correlates With Neoplastic Progression in Barrett's Esophagus. Appl Immunohistochem Mol Morphol 26:552-556
Park, Jae H; Rivière, Isabelle; Gonen, Mithat et al. (2018) Long-Term Follow-up of CD19 CAR Therapy in Acute Lymphoblastic Leukemia. N Engl J Med 378:449-459

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