Drug Delivery and Molecular Sensing (DDMS) Research Program Project Summary The Drug Delivery and Molecular Sensing (DDMS) Research Program aims to provide physical science/engineering and technology solutions to advance the understanding of cancer biology, and to improve prevention, detection and treatment of cancers. These solutions integrate Purdue Center for Cancer Research (PCCR) Foundational Disciplines into collaborative studies that are launched from DDMS-associated expertise, including molecular conjugates and nanoparticles for targeted drug delivery, new imaging modalities for surgical guidance and drug sensitivity, and new in vitro tumor models to study cancer biology. To accomplish future goals, the DDMS Program will pursue three scientific themes that are embodied in its specific aims.
Aim 1 : Next generation therapeutic delivery systems to precisely administer anti-cancer agents Aim 2: Ultra-precision sensing and imaging techniques and devices for early detection and prognosis Aim 3: Innovative enabling technologies for research across the cancer spectrum The program is comprised of 31 faculty members from 13 Purdue University academic departments. Members of the DDMS Program synergistically collaborate with other PCCR Research Programs, as demonstrated by strong inter-programmatic publications (20%). DDMS is highly productive, having generated 370 cancer-relevant publications between July 2015 and July 2019. Among these publications, 58% represent collaborative work. DDMS efforts are sustained by $4.6 million (direct) in peer-reviewed, cancer-relevant funding in the last budget year. In addition, 86 patents and five start-up companies were created. To facilitate this highly multidisciplinary Research Program, the Program Leaders (Drs. Bumsoo Han and Yoon Yeo) have been working on promoting collaborative research and integrating biological sciences and engineering disciplines. Notable outcomes of investigations during the current funding period are new nanoparticle formulations targeting both cancer and immune cells within the tumor microenvironment, ligand-targeted imaging and therapeutic agents, a new intraoperative image-guidance technique based on spectroscopy, and a new imaging modality to assess the chemosensitivity of tumor tissues. In addition, new in vitro tumor models have been developed to identify and validate new drug targets for pancreatic cancer and to perform research on drug resistance and tumor onset for breast cancer. During the next funding period, DDMS leadership will pursue four initiatives: (1) continued excellence in drug delivery and molecular sensing; (2) accelerated validation of sensing and imaging technologies with preclinical models; (3) building on computational and data science expertise for cancer biology and drug discovery; and (4) development of greater strength in physical science/engineering for oncology.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA023168-40
Application #
10024921
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-08-01
Budget End
2021-06-30
Support Year
40
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Purdue University
Department
Type
DUNS #
072051394
City
West Lafayette
State
IN
Country
United States
Zip Code
47907
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Bhandari, Pushpak; Novikova, Gloriia; Goergen, Craig J et al. (2018) Ultrasound beam steering of oxygen nanobubbles for enhanced bladder cancer therapy. Sci Rep 8:3112
Dhawan, Deepika; Hahn, Noah M; Ramos-Vara, José A et al. (2018) Naturally-occurring canine invasive urothelial carcinoma harbors luminal and basal transcriptional subtypes found in human muscle invasive bladder cancer. PLoS Genet 14:e1007571
Shinde, Aparna; Libring, Sarah; Alpsoy, Aktan et al. (2018) Autocrine Fibronectin Inhibits Breast Cancer Metastasis. Mol Cancer Res 16:1579-1589
Ghosh, Arun K; Ghosh, Koena; Brindisi, Margherita et al. (2018) Design, synthesis, X-ray studies, and biological evaluation of novel BACE1 inhibitors with bicyclic isoxazoline carboxamides as the P3 ligand. Bioorg Med Chem Lett 28:2605-2610
Thompson, Taylor J; Han, Bumsoo (2018) Analysis of adhesion kinetics of cancer cells on inflamed endothelium using a microfluidic platform. Biomicrofluidics 12:042215
Alpsoy, Aktan; Dykhuizen, Emily C (2018) Glioma tumor suppressor candidate region gene 1 (GLTSCR1) and its paralog GLTSCR1-like form SWI/SNF chromatin remodeling subcomplexes. J Biol Chem 293:3892-3903
Larocque, Elizabeth A; Naganna, N; Opoku-Temeng, Clement et al. (2018) Alkynylnicotinamide-Based Compounds as ABL1 Inhibitors with Potent Activities against Drug-Resistant CML Harboring ABL1(T315I) Mutant Kinase. ChemMedChem 13:1172-1180
Kumari, Rashmi; Silic, Martin R; Jones-Hall, Yava L et al. (2018) Identification of RECK as an evolutionarily conserved tumor suppressor gene for zebrafish malignant peripheral nerve sheath tumors. Oncotarget 9:23494-23504
VerHeul, Ross; Sweet, Craig; Thompson, David H (2018) Rapid and simple purification of elastin-like polypeptides directly from whole cells and cell lysates by organic solvent extraction. Biomater Sci 6:863-876

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