The intronic G13964C variant in p53 is not a high-risk mutation in familial breast cancer in Australia View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2001-07-17

AUTHORS

Anna Marsh, Amanda B Spurdle, Bruce C Turner, Sian Fereday, Heather Thorne, Gulietta M Pupo, Graham J Mann, John L Hopper, Joseph F Sambrook, Georgia Chenevix-Trench, Australian Breast Cancer Family Study (ABCFS) and Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (kConFaB)

ABSTRACT

BackgroundMutations in BRCA1 and BRCA2 account for approximately 50% of breast cancer families with more than four affected cases, whereas exonic mutations in p53, PTEN, CHK2 and ATM may account for a very small proportion. It was recently reported that an intronic variant of p53 - G13964C - occurred in three out of 42 (7.1%) 'hereditary' breast cancer patients, but not in any of 171 'sporadic' breast cancer control individuals (P = 0.0003). If this relatively frequent occurrence of G13964C in familial breast cancer and absence in control individuals were confirmed, then this would suggest that the G13964C variant plays a role in breast cancer susceptibility.MethodWe genotyped 71 familial breast cancer patients and 143 control individuals for the G13964C variant using polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP) analysis.ResultsThree (4.2%; 95% confidence interval [CI] 0–8.9%) G13964C heterozygotes were identified. The variant was also identified in 5 out of 143 (3.5%; 95% CI 0.6–6.4%) control individuals without breast cancer or a family history of breast cancer, however, which is no different to the proportion found in familial cases (P = 0.9).ConclusionThe present study would have had 80% power to detect an odds ratio of 4.4, and we therefore conclude that the G13946C polymorphism is not a 'high-risk' mutation for familial breast cancer. More... »

PAGES

346

Identifiers

URI

http://scigraph.springernature.com/pub.10.1186/bcr319

DOI

http://dx.doi.org/10.1186/bcr319

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1045226989

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/11597326


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