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No germline TP53 mutations detected in familial and bilateral testicular cancer.

作者信息

Heimdal K, Lothe R A, Lystad S, Holm R, Fosså S D, Børresen A L

机构信息

Department of Genetics, Norwegian Radium Hospital, Oslo.

出版信息

Genes Chromosomes Cancer. 1993 Feb;6(2):92-7. doi: 10.1002/gcc.2870060205.

DOI:10.1002/gcc.2870060205
PMID:7680893
Abstract

Mutations in the TP53 gene are considered to be among the most common genetic alterations in human cancers. Both somatic and germline mutations have been found. Using polymerase chain reaction (PCR), constant denaturant gel electrophoresis (CDGE), and denaturing gradient gel electrophoresis (DGGE), we have examined 32 patients with bilateral and familial germ cell tumors (GCT) and two patients with sporadic GCT for germline mutations within the conserved regions of the gene. In addition, 15 tumors were screened for somatic mutations and analyzed for loss of heterozygosity (LOH) at the TP53 locus. Twelve tumors were analyzed for expression of TP53 via immunohistochemistry. Neither germline nor somatic TP53 mutations were detected. LOH was observed in one of five informative cases. No tumors showed increased expression of TP53 protein. These results indicate that alterations in the TP53 gene are not important for the predisposition to and development of GCT.

摘要

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