In this competing continuation application we propose to extend our investigation of Photodynamic Therapy (PDT). Three of the proposed projects are directed at elucidating the mechanisms by which PDT elicits cellular/tissue response when employed in cancer treatment. Each follows a distinctly different approach to achieve its goals; in subsequent years, each interacts with the other projects. One project deals specifically with non invasive methods to ultimately improve the utility of PDT and one with the extension of fundamental laboratory data into a primary tumor, veterinary clinical trial. Specifically, the projects in this proposal propose to: 1) examine the mechanisms of interaction between PDT and hyperthermia; 2) extend results obtained in laboratory models to spontaneous veterinary tumors; 3) develop a PDT resistant tumor model and subsequently elucidate the mechanisms involved in such resistance; 4) develop non invasive methods to quantitate tissue photosensitizer concentrations; and 5) to establish a quantifiable measure of true tissue photosensitivity to allow the intercomparison of various PDT treatments. This program is a multidisciplinary, multi-institutional investigation aimed at understanding and improving the use of PDT for the treatment of cancer. The inter-relation between the constituent projects enhances the overall effort.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA043892-05
Application #
3094093
Study Section
Special Emphasis Panel (SRC (V1))
Project Start
1987-09-01
Project End
1997-03-31
Budget Start
1993-05-10
Budget End
1994-03-31
Support Year
5
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Henry Ford Health System
Department
Type
DUNS #
073134603
City
Detroit
State
MI
Country
United States
Zip Code
48202
Wang, Luo-Wei; Huang, Zheng; Lin, Han et al. (2013) Effect of Photofrin-mediated photocytotoxicity on a panel of human pancreatic cancer cells. Photodiagnosis Photodyn Ther 10:244-251
Lei, Tim C; Pendyala, Srinivas; Scherrer, Larry et al. (2013) Optical profiles of cathode ray tube and liquid crystal display monitors: implication in cutaneous phototoxicity in photodynamic therapy. Appl Opt 52:2711-7
Weston, Mark A; Patterson, Michael S (2011) Calculation of singlet oxygen dose using explicit and implicit dose metrics during benzoporphyrin derivative monoacid ring A (BPD-MA)-PDT in vitro and correlation with MLL cell survival. Photochem Photobiol 87:1129-37
Santra, Manoranjan; Zheng, Xuguang; Roberts, Cindi et al. (2010) Single doublecortin gene therapy significantly reduces glioma tumor volume. J Neurosci Res 88:304-14
Singh, Gurmit; Alqawi, Omar; Espiritu, Myrna (2010) Metronomic PDT and cell death pathways. Methods Mol Biol 635:65-78
Zhang, Xuepeng; Zheng, Xuguang; Jiang, Feng et al. (2009) Dual-color fluorescence imaging in a nude mouse orthotopic glioma model. J Neurosci Methods 181:178-85
Katakowski, Mark; Jiang, Feng; Zheng, XuGuang et al. (2009) Tumorigenicity of cortical astrocyte cell line induced by the protease ADAM17. Cancer Sci 100:1597-604
Weston, Mark A; Patterson, Michael S (2009) Simple photodynamic therapy dose models fail to predict the survival of MLL cells after HPPH-PDT in vitro. Photochem Photobiol 85:750-9
Zheng, Xuguang; Jiang, Feng; Katakowski, Mark et al. (2009) ADAM17 promotes breast cancer cell malignant phenotype through EGFR-PI3K-AKT activation. Cancer Biol Ther 8:1045-54
Hong, Xin; Jiang, Feng; Kalkanis, Steven N et al. (2009) Intracellular free calcium mediates glioma cell detachment and cytotoxicity after photodynamic therapy. Lasers Med Sci 24:777-86

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