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Plenary Sessions





        PLENARY TITLE: NANO ASPECTS IN THE PHYSICS OF CANCER:   quantify delivery, the use of magnetic resonance imaging (MRI) for
        FROM NUCLEAR REMODELING TO SELF-RECOGNITION FOR         anatomic and functional imaging and to assess local temperature and the
        GENE/DRUG DELIVERY                                      use of ultrasound to enhance delivery. Using this combination of tech-
                        Date/Time: Monday, February 22, 02:30 -03:15 PM   niques, we have developed activatable particles for the delivery of
                                          Location: Grand Ballroom  chemotherapeutics in cancer and targeted nanovehicles for the delivery
                      Presenter: Dennis Discher, University of Pennsylvania  of miRNA in cardiovascular disease. Our cancer focus has involved
                                                                identifying nanodelivery strategies that are curative for local disease and
                      Session Description: Tissue cells, implants, and   strategies that synergize with immunotherapy for the treatment of systemic
                      particles of any type interact with the innate immune   disease. We have developed methods to load activatable particles with a
                      system, especially phagocytes that try to ‘eat’   metal-drug complex and to release this complex by increasing the local
                      everything. However, ‘Self’ cells are spared due to a   temperature using ultrasound. Full release of the chemotherapeutic
                      polypeptide found on all cells that marks cells (as well   occurs only in the region of elevated temperature and in the presence of a
        as engineered viruses and particles) as ‘Self’, limiting their phagocytic   reduced pH. We find that such a strategy enhances efficacy while
        clearance in vitro and in vivo. The phagocyte’s cytoskeleton drives the   reducing systemic toxicity. We will describe both the nanotherapeutic
        decision downstream of adhesion. If an injected cell is recognized as ‘Self’   strategies and the imaging systems that facilitate this approach. In
        and if it has stem-like properties, then further interactions with the   addition, we have recently explored the use of targeted, coated cationic
        surrounding tissue can influence its differentiation. Matrix elasticity is one   particles to facilitate the delivery of biologic therapeutics to endothelial
        physical feature that directs stem cell fate and reflects the fact that tissues   cells and will demonstrate the imaging approaches required for the
        can be very soft like fat and brain, or increasingly stiff like striated muscle   optimization of such a design and the resulting efficacy in cardiovascular
        and rigid like bone. Stem and progenitor cells use myosin-II to feel and   disease.
        respond to such elasticity differences, with physical signals propagating all
        the way into the nucleus, which feeds back on gene expression. What   Bio: Katherine Whittaker Ferrara is a Distinguished Professor of Biomedical
        unifies these mechanisms of immune or matrix recognition is a conver-  Engineering at UC Davis and the Director of theCenter for Content Rich
        gence of decision-making pathways on cytoskeletal force generation.  Evaluation of Therapeutic Efficacy (cCRETE). She is a member of the
                                                                National Academy of Engineering and a fellow of the IEEE, American
        Bio: Dennis E. Discher is the Robert D. Bent Chair Professor and Director of   Association for the Advancement of Science, the Biomedical Engineering
        the NCI-funded Physical Sciences Oncology Center at the University of   Society, the Acoustical Society of America and the American Institute of
        Pennsylvania. He received a Ph.D. jointly from the University of California,   Medical and Biological Engineering. She currently chairs the Clinical
        Berkeley and San Francisco in 1993 for biophysical studies of cell   Molecular Imaging Probes (CMIP) NIH study section. Dr. Ferrara received
        membranes, and was a U.S. National Science Foundation International   her Ph.D. in 1989 from the University of California, Davis. Prior to her PhD,
        Fellow in computational biophysics at the University of British Columbia   Dr. Ferrara was a project engineer for General Electric Medical Systems,
        until 1996. He has coauthored more than 200 publications with >30,000   involved in the development of early magnetic resonance imaging and
        citations that range in topic from matrix effects on stem cells and physical   ultrasound systems. Following an appointment as an Associate Professor
        properties of the cell nucleus to mechanisms of ‘self’ recognition by   in the Department of Biomedical Engineering at the University of Virginia,
        macrophages and self-assembling polymers applied to disease, with   Charlottesville, Dr. Ferrara served as the founding chair of the Department
        papers appearing in Science, Cell, and various Nature journals. ISI lists   of Biomedical Engineering at UC Davis. Her laboratory is known for early
        ‘Matrix elasticity directs stem cell lineage specification’ (Cell 2006) as the   work in aspects of ultrasonics and has more recently expanded their focus
        3rd most cited experimental research paper in the field of Molecular   to broadly investigate molecular imaging and drug delivery. Dr. Ferrara’s
        Biology & Genetics since 2004. Additional honors and service include:   laboratory has received numerous awards including the Achievement
        election to the U.S. National Academy of Engineering, a Presidential Early   Award from the IEEE Ultrasonics, Ferroelectrics and Frequency Control
        Career Award for Scientists and Engineers from the U.S. National Science   Society, which is the top honor of this society.
        Foundation, the Friedrich Wilhelm Bessel Award from the Humboldt
        Foundation of Germany, a LabEx Visiting Fellow at the Institut Jacques
        Monod – Paris, and membership on the Editorial Board for Science.
                                                                PLENARY TITLE: DIRECT CELL REPROGRAMMING VIA GENOME
                                                                EDITING
                                                                               Date/Time: Tuesday, February 23, 02:30-03:15 PM
        PLENARY TITLE: IMAGE-GUIDED NANOTHERAPY IN THE                                           Location: Grand Ballroom
        TREATMENT OF CANCER AND CARDIOVASCULAR DISEASE                        Presenter: Kam W. Leong, Columbia University
                        Date/Time: Tuesday, February 23, 08:30-09:15 AM
                                          Location: Grand Ballroom            Bio: Kam W. Leong is the Samuel Y. Sheng Professor of
                      Presenter: Katherine Whittaker Ferrara, University of   Biomedical Engineering at Columbia University. His
                      California, Davis                                       lab works on nanoparticle-mediated nonviral gene
                                                                              delivery and immunotherapy—from design and
                      Session Description: In vivo imaging can greatly        synthesis of new carriers to applications for hemophil-
                      enhance the optimization of nanodelivery methods. In   ia and infectious diseases. The lab also works on the application of   13
                      our laboratory, we combine the use of positron   nanostructured biomaterials for regenerative medicine, particularly on
                      emission tomography (PET) and optical imaging to   understanding cell-topography interactions and on the application of
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