An unexpected caffeine-enhanced survival in x-ray-sensitive variant cells
Description
The sensitivity of normal Chinese hamster cell lines, V79 and CHO, mouse cell lines, L5178Y and L, and human HeLa cells to the killing effect of x-ray is enhanced with addition of caffeine following x-ray irradiation in a dose-dependent fashion. However, the survival rate of variant cell (V79-AL162/S-10) increased with addition of low concentration of caffeine (caffeine-enhanced survival phenomenon). Therefore, the effects of protein synthesis-inhibiting agents, such as cycloheximide and puromycin, on caffeine-enhanced survival phenomenon were examined. This phenomenon was completely abolished by the inhibitory agents, but not abolished by DNA synthesis-damaging agents, such as excess thymidine and aphidicolin. DNA-damaging physiochemical factors, such as neutrons, U.V., methyl methanesulfonate and mitomycin C, were examined in relation to variant cells' sensitivity and caffeine-enhanced survival phenomenon. V79-AL162/S-10 cells showed high sensitivity to the killing effect of mitomycin C, but their survival rate returned to the rate of normal V79-B310H cells with addition of caffeine. (Namekawa, K.)
Additional details
Publishing Information
- Imprint Title
- Proceedings of the 15th NIRS symposium on radiation-induced genetic damage and risk assessment: biomedical approaches
- Imprint Pagination
- 332 p.
- Journal Page Range
- p. 155-159.
- Report number
- NIRS-M--54
Conference
- Title
- 15. NIRS symposium.
- Dates
- 15-16 Mar 1984.
- Place
- Chiba (Japan).
INIS
- Country of Publication
- Japan
- Country of Input or Organization
- Japan
- INIS RN
- 18031333
- Subject category
- S63: RADIATION, THERMAL, AND OTHER ENVIRONMENTAL POLLUTANT EFFECTS ON LIVING ORGANISMS AND BIOLOGICAL MATERIALS;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- ANIMAL CELLS; BIOLOGICAL PATHWAYS; CAFFEINE; CELL CULTURES; CELL KILLING; DNA REPAIR; MUTANTS; RADIOSENSITIVITY; SURVIVAL CURVES; X RADIATION
- Descriptors DEC
- ANALEPTICS; BIOLOGICAL RECOVERY; BIOLOGICAL REPAIR; CENTRAL NERVOUS SYSTEM AGENTS; DRUGS; ELECTROMAGNETIC RADIATION; HETEROCYCLIC COMPOUNDS; IONIZING RADIATIONS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC OXYGEN COMPOUNDS; PURINES; RADIATIONS; XANTHINES