Literature DB >> 19556618

High frequency of de novo mutations in Li-Fraumeni syndrome.

K D Gonzalez, C H Buzin, K A Noltner, D Gu, W Li, D Malkin, S S Sommer.   

Abstract

BACKGROUND: Li-Fraumeni syndrome is an autosomal dominant cancer predisposition syndrome caused by germline mutations in the TP53 gene. The frequency of germline de novo TP53 mutations is largely unknown; few unequivocal de novo mutations have been reported. METHODS AND
RESULTS: Of 341 patients with early onset cancer sent for clinical testing to a national reference laboratory, 75 patients had TP53 germline mutations. Five (7%) de novo mutations were identified, as well as an additional 10 TP53 germline mutations likely to be de novo by family history. The frequency of de novo TP53 mutations in this patient sample is at least 7% and may be as high as 20%.
CONCLUSIONS: The possibility that de novo germline TP53 mutations are relatively common has implications for testing and the identification of potential Li-Fraumeni syndrome in patients with little or no family history of cancer.

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Year:  2009        PMID: 19556618     DOI: 10.1136/jmg.2008.058958

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  55 in total

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4.  Risks of first and subsequent cancers among TP53 mutation carriers in the National Cancer Institute Li-Fraumeni syndrome cohort.

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5.  Nearly Half of TP53 Germline Variants Predicted To Be Pathogenic in Patients With Osteosarcoma Are De Novo: A Report From the Children's Oncology Group.

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6.  The first two confirmed sub-Saharan African families with germline TP53 mutations causing Li-Fraumeni syndrome.

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7.  Prevalence of germline TP53 mutations in HER2+ breast cancer patients.

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Review 8.  Clinical Outcomes of TP53 Mutations in Cancers.

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Authors:  April D Sorrell; Carin R Espenschied; Julie O Culver; Jeffrey N Weitzel
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