Paper
10 March 2015 Macrophage mediated PCI enhanced gene-directed enzyme prodrug therapy
Catherine E. Christie M.D., Genesis Zamora, Young J. Kwon, Kristian Berg, Steen J. Madsen, Henry Hirschberg M.D.
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Abstract
Photochemical internalization (PCI) is a photodynamic therapy-based approach for improving the delivery of macromolecules and genes into the cell cytosol. Prodrug activating gene therapy (suicide gene therapy) employing the transduction of the E. coli cytosine deaminase (CD) gene into tumor cells, is a promising method. Expression of this gene within the target cell produces an enzyme that converts the nontoxic prodrug, 5-FC, to the toxic metabolite, 5-fluorouracil (5-FU). 5-FC may be particularly suitable for brain tumors, because it can readily cross the bloodbrain barrier (BBB). In addition the bystander effect, where activated drug is exported from the transfected cancer cells into the tumor microenvironment, plays an important role by inhibiting growth of adjacent tumor cells. Tumor-associated macrophages (TAMs) are frequently found in and around glioblastomas. Monocytes or macrophages (Ma) loaded with drugs, nanoparticles or photosensitizers could therefore be used to target tumors by local synthesis of chemo attractive factors. The basic concept is to combine PCI, to enhance the ex vivo transfection of a suicide gene into Ma, employing specially designed core/shell NP as gene carrier.
© (2015) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Catherine E. Christie M.D., Genesis Zamora, Young J. Kwon, Kristian Berg, Steen J. Madsen, and Henry Hirschberg M.D. "Macrophage mediated PCI enhanced gene-directed enzyme prodrug therapy", Proc. SPIE 9305, Optical Techniques in Neurosurgery, Neurophotonics, and Optogenetics II, 93050C (10 March 2015); https://doi.org/10.1117/12.2082590
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KEYWORDS
Tumors

Nose

Imaging systems

Linear filtering

Sensors

Channel projecting optics

Convolution

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