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13 July 2009Combination of vascular targeting PDT with combretastatin A4 phosphate
Tumor vasculature is an attractive target for cancer therapy due to its accessibility to blood-borne therapeutic agents and
the dependence of tumor cells on a functional blood supply for survival and growth. Vascular targeting photodynamic
therapy (vPDT) is a novel modality based on the selective laser light activation of photosensitizers localized inside tumor
vasculature to shutdown tumor vascular function. Although this vascular targeting therapy is showing great promise for
cancer treatment, tumor recurrence has been observed in both preclinical and clinical studies. In this study, we intend to
enhance the therapeutic outcome of vascular targeting PDT by combining it with combretastatin A4 phosphate (CA4P), a
blood flow inhibitor. We found that the combination of CA4P and vPDT significantly increased endothelial cell
apoptosis than each single therapy. Western blot analysis suggests that myosin light chain kinase (MLCK) is a common
target of CA4P and vPDT. In a PC-3 prostate tumor model, we found that CA4P was able to greatly enhance tumor
response to vPDT. These results demonstrate that CA4P and vPDT can be combined to enhance the therapeutic effect.
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Chong He, Babasola Fateye, Bin Chen, "Combination of vascular targeting PDT with combretastatin A4 phosphate," Proc. SPIE 7380, Photodynamic Therapy: Back to the Future, 738032 (13 July 2009); https://doi.org/10.1117/12.822969