Disease family history and modification of breast cancer risk in common BRCA2 variants

  • Authors:
    • Ian Jonathan Seymour
    • Silvia Casadei
    • Valentina Zampiga
    • Simonetta Rosato
    • Rita Danesi
    • Fabio Falcini
    • Miria Strada
    • Nori Morini
    • Carlo Naldoni
    • Angelo Paradiso
    • Stefania Tommasi
    • Francesco Schittulli
    • Dino Amadori
    • Daniele Calistri
  • View Affiliations

  • Published online on: March 1, 2008     https://doi.org/10.3892/or.19.3.783
  • Pages: 783-786
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Abstract

A number of BRCA1 and BRCA2 polymorphisms have been extensively studied in order to test their association with breast cancer risk. Subsequently, discordant results were reported. In the present study, the genotypes of one BRCA1 (Q356R) and three BRCA2 (203G>A, N372H, IVS21-66T>C) common variants were evaluated in a series of 252 breast cancer patients, 155 age-matched controls and analysed in relation to family history (low- or high-risk) and BRCA1/2 mutation status. A complete analysis of the BRCA1/2 coding regions was performed on the 217 women from high-risk families and 44 BRCA1/2 mutation carriers were identifed. According to a dominant inheritance model, the BRCA2 IVS21-66T>C variant showed a 1.79-fold (95% CI, 1.16-2.78; P=0.009) increased breast cancer risk for the overall series. The BRCA2 N372H polymorphism was associated with a 2.29-fold (95% CI, 1.16-4.49; P=0.016) increased risk in the subgroup of high-risk families with no BRCA1/2 mutations. Conversely, the BRCA1 Q356R and BRCA2 203G>A polymorphisms did not show any significant associations with breast cancer risk. In conclusion, the analysis of some BRCA2 variants could help to identify women at a higher risk of developing breast cancer who could be candidates for chemoprevention protocols.

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March 2008
Volume 19 Issue 3

Print ISSN: 1021-335X
Online ISSN:1791-2431

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Spandidos Publications style
Seymour IJ, Casadei S, Zampiga V, Rosato S, Danesi R, Falcini F, Strada M, Morini N, Naldoni C, Paradiso A, Paradiso A, et al: Disease family history and modification of breast cancer risk in common BRCA2 variants. Oncol Rep 19: 783-786, 2008.
APA
Seymour, I.J., Casadei, S., Zampiga, V., Rosato, S., Danesi, R., Falcini, F. ... Calistri, D. (2008). Disease family history and modification of breast cancer risk in common BRCA2 variants. Oncology Reports, 19, 783-786. https://doi.org/10.3892/or.19.3.783
MLA
Seymour, I. J., Casadei, S., Zampiga, V., Rosato, S., Danesi, R., Falcini, F., Strada, M., Morini, N., Naldoni, C., Paradiso, A., Tommasi, S., Schittulli, F., Amadori, D., Calistri, D."Disease family history and modification of breast cancer risk in common BRCA2 variants". Oncology Reports 19.3 (2008): 783-786.
Chicago
Seymour, I. J., Casadei, S., Zampiga, V., Rosato, S., Danesi, R., Falcini, F., Strada, M., Morini, N., Naldoni, C., Paradiso, A., Tommasi, S., Schittulli, F., Amadori, D., Calistri, D."Disease family history and modification of breast cancer risk in common BRCA2 variants". Oncology Reports 19, no. 3 (2008): 783-786. https://doi.org/10.3892/or.19.3.783