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Stem Cells, Vol 13, 77-85, Copyright © 1995 by AlphaMed Press
ORIGINAL ARTICLES |
N Zaffaroni, E Benini, D Gornati, A Bearzatto and R Silvestrini
Istituto Nazionale per lo Studio e la Cura dei Tumori, Milano, Italy.
We investigated the possible relationship between immunohistochemically detected p53 expression and in vitro response to gamma-irradiation in 24 primary cultures of human ovarian cancers and cutaneous melanomas. The frequency of p53-positive tumors was around 60% within each tumor histotype. The range of the surviving fraction at 2 Gy (SF2) was similar in p53-positive (0.10-0.76) and p53-negative (0.23-0.65) tumors, with median values of 0.36 and 0.33, respectively. No differences were observed in the accumulation of DNA-double strand breaks, assessed by neutral filter elution after exposure to 50 Gy, between p53-positive and p53-negative tumors. As regards DNA lesion repair, after 2 h of recovery the percentage of rejoined DNA-double strand breaks ranged from 19% to 99% in the different cultures, but again the distribution of values was similar for p53-positive and p53- negative tumors. Specifically, the median percentage of repaired DNA- double strand breaks was 70% and 74% in the two groups. On the whole, our data do not support the hypothesis that p53 overexpression is a major determinant of in vitro radiation response.
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J. M. Brown and B. G. Wouters Apoptosis, p53, and Tumor Cell Sensitivity to Anticancer Agents Cancer Res., April 1, 1999; 59(7): 1391 - 1399. [Abstract] [Full Text] [PDF] |
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