The experiments proposed in this application focus on the mechanistic basis for damage from ionizing radiation. We specifically ask """"""""How does radiation damage the cell?"""""""" """"""""What role do radiolytic products play in this damage?"""""""" """"""""How does oxygen function as a radiation sensitizer?"""""""" We plan experiments with bacteria (multiple strains of E. coli), the mammalian (human) erythrocyte, and a chemical assay for measuring the radiolytic yeilds of hydrogen peroxide. Because an organism's overall response to ionizing radiation involves many factors, complementary experiments with different types of cells are required. Bacterial spores are metabolically inactive and, therefore, enzymatically directed repair is not possible. Our past work with spores identifies the kinds of radiation-induced damage which can occur. Complementary experiments with different mutant strains of bacteria will allow us to judge whether or not we can associate a specific type of repair with a particular kind of radiation-induced damage. Work with cell membranes will show whether or not we can identify a specific cellular target for damage from ionizing radiation. Although these experiments involve chemical systems and procaryotic cells, the required parallel work with in vitro mammalian cells is underway (1 RO 1 CA-28932). The information we gain with these biological and chemical systems should have immediate clinical relevance. Our long-range goals involve applying this information to select and test sensitizers in combination with oxygen. When sensitizers are found which function differently from oxygen, the overall effect from combinations of oxygen and such a sensitizer should be at a maximun. This means we would achieve a higher clinical effectiveness when tumors containing cells at low oxygen concentrations are treated. The basis for such an application is a thorough knowledge of how radiation damages cells and how oxygen functions as a radiation sensitizer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
1R01CA030921-01A3
Application #
3169395
Study Section
Radiation Study Section (RAD)
Project Start
1985-09-01
Project End
1988-08-31
Budget Start
1985-09-01
Budget End
1986-08-31
Support Year
1
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Hahnemann University
Department
Type
Schools of Medicine
DUNS #
City
Philadelphia
State
PA
Country
United States
Zip Code
19129
Ewing, D; Guilfoil, D S (1991) Is N2O-dependent damage 'fixed' by action of the recA locus? Int J Radiat Biol 59:145-51
Ewing, D; Guilfoil, D S; Ohm, M B (1991) Do intracellular thiol or peroxidase levels block radiation sensitization by nitrous oxide in some E. coli strains? Int J Radiat Biol 59:153-64
Ewing, D; Walton, H L; Guilfoil, D S et al. (1991) The relationship between the anoxic sensitivity and the extent of sensitization by nitrous oxide. Int J Radiat Biol 59:717-27
Ewing, D; Guilfoil, D S (1989) Additivity in the sensitizing effects of nitrous oxide and oxygen. Radiat Res 120:294-305
Ewing, D (1987) Radiation sensitization of E. coli B/r by mixtures of oxygen and nitrous oxide. Int J Radiat Biol Relat Stud Phys Chem Med 52:921-33
Ewing, D; Kubala, G J (1987) Radiation protection of Escherichia coli B/r by hydroxyl radical scavengers. Radiat Res 109:256-74
Ewing, D; Jones, S R (1987) Superoxide removal and radiation protection in bacteria. Arch Biochem Biophys 254:53-62