TP53 Mutations in Canine Brain Tumors

被引:26
|
作者
York, D. [1 ]
Higgins, R. J. [2 ]
LeCouteur, R. A. [1 ]
Wolfe, A. N. [1 ]
Grahn, R. [3 ]
Olby, N. [4 ]
Campbell, M. [1 ]
Dickinson, P. J. [1 ]
机构
[1] Univ Calif Davis, Dept Surg & Radiol Sci, Sch Vet Med, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Pathol Microbiol & Immunol, Sch Vet Med, Davis, CA 95616 USA
[3] Univ Calif Davis, Dept Populat Hlth & Reprod, Sch Vet Med, Davis, CA 95616 USA
[4] N Carolina State Univ, Coll Vet Med, Dept Clin Sci, Raleigh, NC USA
关键词
cancer genes; dog; gDNA; nervous system; oncology; polymerase chain reaction; sequencing; P53; MUTATIONS; SUPPRESSOR GENE; MUTANT P53; CELL-LINES; PROTEIN; AMPLIFICATION; OVEREXPRESSION; FREQUENCY; MDM2; ASTROCYTOMA;
D O I
10.1177/0300985811424734
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The p53 tumor suppressor gene (TP53) is the most frequently altered gene in human cancer. Mutation of the gene has been shown to be an important mechanism of p53 pathway inactivation in a variety of human brain tumors, particularly those of astrocytic origin. Genomic DNA from a series of 37 glial and 51 nonglial canine brain tumors was sequenced to determine the frequency of TP53 gene mutations involving exons 3-9. Exonic mutations were found in 3 of 88 tumors (3.4%) and specifically in 1 of 18 astrocytic tumors (5.5%). This is markedly lower than that reported in comparable human tumors, suggesting that alternative mechanisms of p53 inactivation are likely to be present if p53 function contributes significantly to oncogenesis in canine brain tumors.
引用
收藏
页码:796 / 801
页数:6
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