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[Cancer Research 56, 5365-5368, December 1, 1996]
© 1996 American Association for Cancer Research

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p53-null Cells Are More Sensitive to Ultraviolet Light Only in the Presence of Caffeine1

Jeffrey S. DeFrank, Wei Tang and Simon N. Powell2

Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114

We have shown previously that p53(-/-) fibroblasts show greater sensitization by caffeine to the lethal effects of ionizing radiation compared with p53(+/+) cells. Recently published data have suggested a possible role of p53 in nucleotide excision repair: an association of p53 and xeroderma pigmentosum group B protein and a greater sensitivity to cisplatin of RKO cells transfected with the E6 protein of human papilloma virus (inactivating p53). We show that p53(+/+) and p53(-/-) cells have equal sensitivity to germicidal UV light (as with ionizing radiation). However, the introduction of 2 mM caffeine led to a sensitization enhancement ratio (at 10% survival) of 1.8 in p53(-/-) cells, but only 1.3 in wild-type (p53+/+) cells. Lower doses of caffeine had less effect, and 0.1 mM caffeine resulted in no detectable sensitization of either cell type to UV light in contrast to X-rays. The differential sensitivity of p53(-/-) cells to X-rays and caffeine was thought to be due to override of the G2-M block to cell cycle progression. In response to UV light, cells accumulate in S phase, and the magnitude of S-phase accumulation was observed to be greater in p53(-/-) cells. Caffeine had little effect on the cell cycle distribution in p53(+/+) cells. However, for p53(-/-) cells, a greater proportion were in S phase after treatment with caffeine, and a complete loss of S-phase delay was observed after UV irradiation. In conclusion, the role of p53 in nucleotide excision repair appears to be of little significance for cell survival. Greater sensitization of p53(-/-) cells to caffeine could be mediated via override of S-phase delay.

1 This research was supported by Public Health Service Grant CA58985 from NIH.

2 To whom requests for reprints should be addressed, at Department of Radiation Oncology, Cox 302, 100 Blossom Street, Massachusetts General Hospital, Boston, MA 02114. Phone: (617) 726-8669; Fax: (617) 726-3603; E-mail: powell.simon@mgh.harvard.edu.

Received 8/14/96. Accepted 10/17/96.




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Copyright © 1996 by the American Association for Cancer Research.