No germline TP53 mutations detected in familial and bilateral testicular cancer
- 1 February 1993
- journal article
- research article
- Published by Wiley in Genes, Chromosomes and Cancer
- Vol. 6 (2), 92-97
- https://doi.org/10.1002/gcc.2870060205
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 potymerase 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 heterozygocity (LOH) at the TP53 locus. Twelve tumors were analyzed for expression of TP53 via immunohistochemistry. Neither germline nor somatic TP53 mutations were deteeted. 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.Keywords
This publication has 17 references indexed in Scilit:
- Mice deficient for p53 are developmentally normal but susceptible to spontaneous tumoursNature, 1992
- Constant denaturant gel electrophoresis as a rapid screening technique for p53 mutations.Proceedings of the National Academy of Sciences, 1991
- p53 Protein alterations in human testicular cancer including pre‐invasive intratubular germ‐cell neoplasiaInternational Journal of Cancer, 1991
- p53 Mutations in Human CancersScience, 1991
- The p53 tumour suppressor geneNature, 1991
- Constant denaturant gel electrophoresis, a modification of denaturing gradient gel electrophoresis, in mutation detectionMutation Research Letters, 1991
- Are germ cell tumors part of the Li-Fraumeni cancer family syndrome?Cancer Genetics and Cytogenetics, 1989
- High incidence of lung, bone, and lymphoid tumors in transgenic mice overexpressing mutant alleles of the p53 oncogene.Molecular and Cellular Biology, 1989
- A Comparative Study of the Peroxidase-antiperoxidase Method and an Avidin-Biotin Complex Method for Studying Polypeptide Hormones with Radioimmunoassay AntibodiesAmerican Journal of Clinical Pathology, 1981
- Mutation and Cancer: Statistical Study of RetinoblastomaProceedings of the National Academy of Sciences, 1971