This project is designed to provide information on mechanism(s) of cell death induced by photodynamic therapy (PDT). The long-range goal is an understanding of the selective tumor eradication mediated by PDT. We have classified photosensitizing agents based on their sub-cellular targets: bcl-2, lysosomes, the plasma membrane, or combinations of these targets. We propose a hypothesis that relates PDT targets to death mechanisms: Sensitizers that target bcl-2 can initiate apoptosis by removing a barrier to interactions of bak/bax with the mitochondrial membrane. This process is mimicked by the bcl-2 antagonist HA 14-1. The binding of some sensitizers to bcl-2 is such that some anti-oxidants cannot protect the protein from photodamage. Sensitizers that target lysosomes cause the release of proteases leading to cleavage of the pro-apoptotic protein bid to t-bid. The latter promotes bax polymerization, resulting in an apoptotic response. Photosensitizers that target the plasma membrane can catalyze concomitant photodamage to caspases, likely a result of sensitizer relocalization during irradiation. Stress kinase activation is triggered by reactive oxygen species (ROS) and is pertinent only at low PDT doses that are insufficient to initiate the apoptotic program. At high PDT doses, these responses are downstream of caspase-3 activation and the commitment to death. Experiments have been designed to test the elements of this hypothesis, using a variety of murine and human cell lines, both adhering and in suspension culture. We also plan to explore the basis for the finding that PDT that targets bcl-2 spares the close analog bcl-xL. This implies differences in localization or sensitizer:protein affinity and suggests that bcl-xL alone cannot prevent PDT-induced apoptosis. A sub- contract with Dr. Kevin M Smith (Louisiana State University) will provide a supply of sensitizers including a limited synthetic effort directed at preparing agents able to target bcl-2 or bcl-xL. Collaborative arrangements with Drs. Reiners (co- investigator) and Kim (consultant) continue arrangements that have been productive during the previous interval of support.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA023378-24
Application #
6933845
Study Section
Special Emphasis Panel (ZRG1-MEP (03))
Program Officer
Wong, Rosemary S
Project Start
1983-08-01
Project End
2006-06-30
Budget Start
2005-07-01
Budget End
2006-06-30
Support Year
24
Fiscal Year
2005
Total Cost
$221,462
Indirect Cost
Name
Wayne State University
Department
Pharmacology
Type
Schools of Medicine
DUNS #
001962224
City
Detroit
State
MI
Country
United States
Zip Code
48202
Kessel, David (2018) Apoptosis, Paraptosis and Autophagy: Death and Survival Pathways Associated with Photodynamic Therapy. Photochem Photobiol :
Kessel, David; Reiners Jr, John J (2017) Effects of Combined Lysosomal and Mitochondrial Photodamage in a Non-small-Cell Lung Cancer Cell Line: The Role of Paraptosis. Photochem Photobiol 93:1502-1508
Kessel, David (2017) Subcellular Targeting as a Determinant of the Efficacy of Photodynamic Therapy. Photochem Photobiol 93:609-612
Kessel, David (2016) Photodynamic therapy: Promotion of efficacy by a sequential protocol. J Porphyr Phthalocyanines 20:302-306
Kessel, David; Evans, Conor L (2016) Promotion of Proapoptotic Signals by Lysosomal Photodamage: Mechanistic Aspects and Influence of Autophagy. Photochem Photobiol 92:620-3
Kessel, David (2015) Apoptosis and associated phenomena as a determinants of the efficacy of photodynamic therapy. Photochem Photobiol Sci 14:1397-402
Aggarwal, Neha; Santiago, Ann Marie; Kessel, David et al. (2015) Photodynamic therapy as an effective therapeutic approach in MAME models of inflammatory breast cancer. Breast Cancer Res Treat 154:251-62
Kessel, David (2015) Autophagic death probed by photodynamic therapy. Autophagy 11:1941-3
Gibbs, Jaime H; Zhou, Zehua; Kessel, David et al. (2015) Synthesis, spectroscopic, and in vitro investigations of 2,6-diiodo-BODIPYs with PDT and bioimaging applications. J Photochem Photobiol B 145:35-47
Kessel, David; Reiners Jr, John J (2015) Promotion of Proapoptotic Signals by Lysosomal Photodamage. Photochem Photobiol 91:931-6

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