The overall goal of the Sidney Kimmel Comprehensive Cancer Center (SKCCC) Cancer Molecular and Functional Imaging (CMFI) Program is to use molecular and functional imaging to identify novel, imaging- based targets and advance translational applications in biomarker and drug development and treatment. To achieve this overall goal, the CMFI Program has the following four aims that focus on cancer biology and discovery, imaging agent development, biomarkers and clinical evaluation of therapies, target delineation, and drug delivery: (1) To use multimodality molecular and functional imaging to understand cancer and the tumor microenvironment; (2) To integrate chemistry and molecular biology with imaging to develop novel imaging probes, with an emphasis on clinical translation; (3) To develop noninvasive biomarkers to allow early identification of cancer, predict risk, assist in the selection of treatment and detect response; and (4) To use imaging to determine drug delivery. Over the past five years, this aim has significantly expanded to include developing theranostic agents, a key component of the Program's future directions. The identification of specific targets in cancer drives advances in novel, image-guided platforms, such as liposomes and nanoplexes, to delivery siRNA or cDNA to silence or upregulate specific targets and pathways. As a result, the four aims are interrelated within the CMFIP and among other Programs, such as Cancer Biology (CB), Breast and Ovarian Cancer (BOC), and Prostate Cancer (PC). Currently, the CMFI Program has 27 members and expertise that reflects the four Program elements. CMFI Program members have primary appointments in the departments of Radiology and Radiological Science, Biomedical Engineering, and Chemical and Biomolecular Engineering, and hold appointments in four graduate programs. Nineteen faculty members have peer-reviewed funding. A majority of the faculty is housed in the SKCCC Cancer Research Buildings I and II (CRBI/II) complex, and the Program is home to approximately 10 graduate students and 15 Postdoctoral fellows. The Program is supported by $19.8 million total costs of sponsored funding, of which $18.6 million is peer-reviewed. The Program has major interactions with the BOC, PC, Brain Cancer (BC), and Hematologic Malignancies and Bone Marrow Transplantation (HMBMT) Programs, and is expanding into research of pancreatic cancer and lung cancer. The were 617 publications in the CMFI Program. Of these, 202 (33%) were Intra-Programmatic, 148 (24%) were Inter-Programmatic and 149 (24%) publications were multi-institutional collaborations.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA006973-57
Application #
9944517
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-05-01
Budget End
2021-04-30
Support Year
57
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21205
Shrestha, Eva; White, James R; Yu, Shu-Han et al. (2018) Profiling the Urinary Microbiome in Men with Positive versus Negative Biopsies for Prostate Cancer. J Urol 199:161-171
Gordy, James T; Luo, Kun; Francica, Brian et al. (2018) Anti-IL-10-mediated Enhancement of Antitumor Efficacy of a Dendritic Cell-targeting MIP3?-gp100 Vaccine in the B16F10 Mouse Melanoma Model Is Dependent on Type I Interferons. J Immunother 41:181-189
Woodard, Lauren E; Dennis, Cindi L; Borchers, Julie A et al. (2018) Nanoparticle architecture preserves magnetic properties during coating to enable robust multi-modal functionality. Sci Rep 8:12706
Kyker-Snowman, Kelly; Erlanger Avigdor, Bracha; Nasim, Mansoor et al. (2018) A primary breast cancer with distinct foci of estrogen receptor-alpha positive and negative cells derived from the same clonal origin as revealed by whole exome sequencing. Breast Cancer Res Treat 170:425-430
Christenson, Eric S; Antonarakis, Emmanuel S (2018) PARP inhibitors for homologous recombination-deficient prostate cancer. Expert Opin Emerg Drugs 23:123-133
El-Diwany, Ramy; Soliman, Mary; Sugawara, Sho et al. (2018) CMPK2 and BCL-G are associated with type 1 interferon-induced HIV restriction in humans. Sci Adv 4:eaat0843
Lee, Alice J; Montgomery, Madeline C; Patel, Rupa R et al. (2018) Improving Insurance and Health Care Systems to Ensure Better Access to Sexually Transmitted Disease Testing and Prevention. Sex Transm Dis 45:283-286
Bharathy, Narendra; Berlow, Noah E; Wang, Eric et al. (2018) The HDAC3-SMARCA4-miR-27a axis promotes expression of the PAX3:FOXO1 fusion oncogene in rhabdomyosarcoma. Sci Signal 11:
Ambinder, Richard F (2018) A viral protein kinase drug target for tumors? J Clin Invest 128:2197-2198
Huang, Peng; Park, Seyoun; Yan, Rongkai et al. (2018) Added Value of Computer-aided CT Image Features for Early Lung Cancer Diagnosis with Small Pulmonary Nodules: A Matched Case-Control Study. Radiology 286:286-295

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