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1.
Br J Cancer ; 96(2): 336-40, 2007 Jan 29.
Article in English | MEDLINE | ID: mdl-17133269

ABSTRACT

BHD, TP53, and HNF1beta on chromosome 17 were studied in 92 cases of renal cell carcinoma (46 chromophobe, 19 clear cell, 18 oncocytoma, and nine papillary). Six, thirteen, and zero cases had, respectively BHD, TP53, and HNF1beta mutations, (84% mutations involved chromophobe), suggesting a role for BHD and TP53 in chromophobe subtype.


Subject(s)
Carcinoma, Renal Cell/genetics , Genes, p53 , Hepatocyte Nuclear Factor 1-beta/genetics , Kidney Neoplasms/genetics , Mutation , Proteins/genetics , Proto-Oncogene Proteins/genetics , Tumor Suppressor Proteins/genetics , Humans , Polymorphism, Single Nucleotide
3.
Oncogene ; 20(56): 8092-9, 2001 Dec 06.
Article in English | MEDLINE | ID: mdl-11781822

ABSTRACT

Genome alterations of seven secondary tumors (five osteosarcomas, one malignant peripheral sheath nerve tumor, one leiomyosarcoma) occurring in the field of irradiation of patients treated for bilateral retinoblastoma have been studied. These patients were predisposed to develop radiation-induced tumors because of the presence of a germ line mutation in the retinoblastoma gene (RB1). Tumor cells were characterized by a high chromosome instability whereas microsatellites and minisatellites were found to be stable. In all tumors, the normal RB1 allele was lost with the corresponding chromosome 13, whereas the germ line mutated allele was retained. The two alleles of TP53 were inactivated, one by deletion of the short arm of chromosome 17, the other by mutation. As compared with non-radiation-induced tumors, the observed panel of TP53 mutations was uncommon with sites not recurrently found otherwise and a high rate of deletions (3/7). In these predisposed patients, the loss of the single normal allele of RB1 is rather due to the radiation-induced chromosome instability than a direct effect of ionizing radiation.


Subject(s)
Neoplasms, Radiation-Induced/genetics , Retinoblastoma/radiotherapy , Cytogenetic Analysis , Genes, Retinoblastoma , Genes, p53 , Genetic Predisposition to Disease , Humans , In Situ Hybridization, Fluorescence , Infant , Loss of Heterozygosity , Microsatellite Repeats , Minisatellite Repeats , Mutation , Radiation, Ionizing
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