BACKGROUND. p53 is the most highly mutated tumor suppressor gene in human cancers. Recently, p73, a first homologue of p53, was identified and considered to be an imprinted tumor suppressor gene. Thus, we analyzed the possible role of p73 in human prostate cancers. METHODS. We investigated the expre
Genomic and allelic expression status of thep73 gene in human neuroblastoma
✍ Scribed by Barrois, M. ;Eychenne, M.K. ;Terrier-Lacombe, M.J. ;Duarte, N. ;Dubourg, C. ;Douc-Rasy, S. ;Chompret, A. ;Khagad, M. ;Hartmann, O. ;Caput, D. ;B�nard, J.
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 150 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0098-1532
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✦ Synopsis
Background and Procedure. The p53 gene homologue, p73, is located on the 1p36-3 locus, which is frequently deleted in human neuroblastoma (NB). A survey of 61 NB showed that among 33% of informative cases, p73 loss of heterozygosity (LOH) occurred in 7 of 20 (35%). Results. LOH pattern of vicinal markers suggested that the p73 gene could not be considered as the candidate NB suppressor gene. Moreover, comparative measurements of allelic expression in tumors and corresponding pa-tient lymphocytes indicate that pure biallelism is much more frequent in lymphocytes than in tumors (71% vs 30%, P = 0.05), which suggests that disequilibrated allelic expression is associated with NB disease. Conclusion. Therefore, in the p73 LOH NBs, the p73 gene could be altered in the maintained allele not by mutations [Ishimiya et al.:
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