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Advances in Brief

p53 Mutations in C57BL/6J Murine Thymic Lymphomas Induced by γ-Irradiation and N-Methylnitrosourea

Ormond Brathwaite, William Bayona and Elizabeth W. Newcomb
Ormond Brathwaite
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William Bayona
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Elizabeth W. Newcomb
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DOI:  Published July 1992
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Abstract

Genomic DNA from thymus tissue obtained from 47 C57BL/6J animals treated with the DNA alkylating agent N-methylnitrosourea or γ-irradiation were screened for the presence of p53 mutations by using the single strand conformation polymorphism assay. Mutations were detected in 13% (4 of 30) of primary thymic lymphomas but none of 17 early stage lymphomas. The frequency of p53 mutations was the same in tumors induced by N-methylnitrosourea (2 of 15) or by γ-irradiation (2 of 15). Mutations occurred in the highly conserved regions of the p53 gene in exons 5, 7, and 8. G:C to A:T transitions were commonly observed. One of 4 of the tumors analyzed contained two p53 mutations in exons 7 and 8. A previous study of the same tumors showed that ras mutations occurred with high frequency (>50%) (E. W. Newcomb et al., Cancer Res., 48: 5514–5521, 1988). Our data suggest that p53 mutations do not play a major role in carcinogen-induced thymic lymphomas studied here.

Footnotes

  • ↵1 This work was supported by National Cancer Institute Grant CA 40533.

  • ↵2 To whom requests for reprints should be addressed, at Department of Pathology and Kaplan Comprehensive Cancer Center, New York University Medical Center, 550 First Avenue, New York, NY 10016.

  • Received March 16, 1992.
  • Accepted May 13, 1992.
  • ©1992 American Association for Cancer Research.
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July 1992
Volume 52, Issue 13
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p53 Mutations in C57BL/6J Murine Thymic Lymphomas Induced by γ-Irradiation and N-Methylnitrosourea
Ormond Brathwaite, William Bayona and Elizabeth W. Newcomb
Cancer Res July 1 1992 (52) (13) 3791-3795;

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p53 Mutations in C57BL/6J Murine Thymic Lymphomas Induced by γ-Irradiation and N-Methylnitrosourea
Ormond Brathwaite, William Bayona and Elizabeth W. Newcomb
Cancer Res July 1 1992 (52) (13) 3791-3795;
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