Since 2000, Lawrence Livermore National Laboratory (LLNL) and the UC Davis Cancer Center (UCDCC) have collaborated on cancer-related projects of common interest. As a means to continue interactions and to facilitate new partnerships, LLNL and the UCDCC held a one-day retreat at Wente Vineyards on Monday, October 17, 2011. The organizing committee consisted of Kenneth Turteltaub and Amy L. Gryshuk from LLNL, Dennis Matthews from the NSF Center for Biophotonics Science & Technology at UC Davis, and Ralph deVere White, Simon Cherry, Laura Marcu, Joel Kugelmass, and Melanie Bradnam from the UCDCC. The 75 scientists and physicians from LLNL and UCDCC came together with a goal of creating new partnerships to apply unique LLNL capabilities to solve unmet biomedical needs in cancer. The format for the day included morning presentations, a collegial lunch and poster session, followed by an afternoon of breakout discussion sessions in 4 categories: (1) Diagnostic Technologies, (2) Therapeutic Modalities, (3) Inflammation/Immunology, and (4) Systems Biology & Computation. Attendees were pre-assigned to a discussion session as a means to facilitate networking, collaborations, and conversations about potential funding opportunities. By the end of the day several new areas were identified where LLNL may be able to contribute to improving cancer diagnosis and treatment. The intention is that the philanthropic funds donated by Bertha Fitzpatrick, that are designated to help foster LLNL's involvement in cancer research with UC Davis, will be utilized to fund up to three postdoctoral researchers for two-year terms on new LLNL-UCDCC collaborative high-impact projects. Areas of collaboration include high-performance computing, accelerated mass spectrometry, nanolipoprotein technology, and engineering microfluidics capabilities to evaluate biological specimens, to name a few.
#1 – Diagnostic Technologies (including, but not limited to: imaging and spectroscopic detection systems (optical, x-ray, radionuclide, acoustic) at all spatial scales (single molecule to whole human), mass spectrometry, biosensors, lab-on-a-chip, contrast agents, "-omic " and screening technologies etc…)
#2 – Therapeutic Modalities (including, but not limited to: chemical therapies, cellular therapies, immunotherapies, enhanced and localized drug delivery systems, drug discovery platforms, in vitro and artificial tumor systems for studying therapeutic modalities, pharmacogenomics etc…)
#3 – Inflammation/Immunology (Immunotherapy has shown increasing success in cancer therapy. Tapping into the immune system to attack cancer also presents challenges with regard to sustainability and potential toxicities. The use of nanotechnology offers a means of delivery that can circumvent these issues by increasing pharmacokinetics and efficacy of immunomodulatory agents allowing for more selective attack on the cancer.)
#4 – Systems Biology & Computation (Computational models, system based approaches to link drugs to target proteins and down stream side-effects, predict metabolic characteristics of cells, predict protein-drug interactions, and design novel therapeutics.)
"Where do we go from here" – Summary report from the day: