Caffeine enhancement of X-ray killing in cultured human and rodent cells

C. A. Waldren, I. Raskó

Research output: Contribution to journalArticle

82 Citations (Scopus)

Abstract

At 16-20 hr postirradiation incubation with caffeine enhances X-ray killing of rodent and human cells. Cells tested were Chinese hamster ovary (CHO-K1), lung (CHL), V79, mouse L, HeLa S3, human fibroblasts (AF288, TC171, FS9, CRL1166), and a human-hamster hybrid. The effect of caffeine on the X-ray survival curve of these cells was to remove the initial shoulder without significantly altering the mean lethal dose (D0). This action can be achieved at caffeine concentrations which of themselves cause less than 15% killing. In randomly growing CHO-K1 cells the caffeine-sensitive process occurs with a half-time of 2-5 hr after irradiation. These experiments indicate the existence in human and rodent cells of caffeine-inhibited genome repair for X-ray damage.

Original languageEnglish
Pages (from-to)95-110
Number of pages16
JournalRadiation Research
Volume73
Issue number1
Publication statusPublished - 1978

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caffeine
rodents
Caffeine
Rodentia
X-radiation
X-Rays
augmentation
cells
hamsters
x rays
ovaries
CHO Cells
genome
lethal dose
fibroblasts
Chinese hamsters
shoulders
Cricetulus
Cricetinae
lungs

ASJC Scopus subject areas

  • Agricultural and Biological Sciences (miscellaneous)
  • Biophysics
  • Radiology Nuclear Medicine and imaging
  • Radiation

Cite this

Caffeine enhancement of X-ray killing in cultured human and rodent cells. / Waldren, C. A.; Raskó, I.

In: Radiation Research, Vol. 73, No. 1, 1978, p. 95-110.

Research output: Contribution to journalArticle

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