Increased sperm aneuploidy in two male carriers of germline TP53 mutations
Language English Country United States Media print
Document type Case Reports, Journal Article, Research Support, Non-U.S. Gov't
PubMed
21665182
DOI
10.1016/j.cancergen.2011.03.003
PII: S2210-7762(11)00077-9
Knihovny.cz E-resources
- MeSH
- Aneuploidy * MeSH
- Adult MeSH
- Heterozygote * MeSH
- In Situ Hybridization MeSH
- Humans MeSH
- Li-Fraumeni Syndrome genetics MeSH
- Tumor Suppressor Protein p53 genetics MeSH
- Sperm Count MeSH
- Spermatozoa * MeSH
- Germ-Line Mutation * MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Tumor Suppressor Protein p53 MeSH
- TP53 protein, human MeSH Browser
Li-Fraumeni syndrome is a rare autosomal dominant cancer predisposition syndrome characterized by a broad spectrum of tumors. The disorder is caused by germline mutations in the TP53 gene. We studied chromosomes in the sperm of two male carriers of TP53 mutations. We observed increased sperm aneuploidy, mainly concerning the gonosomes when compared to four normal male controls. This observation may correlate with the involvement of the p53 protein in spermatogenesis, with its role in aneuploidy in cancer, and with the occurrence of two cases of Turner syndrome in families with germline TP53 mutations reported in the literature.
References provided by Crossref.org