Triple‑negative breast cancer frequency and type of BRCA mutation: Clues from Sardinia

  • Authors:
    • Grazia Palomba
    • Mario Budroni
    • Nina Olmeo
    • Francesco Atzori
    • Maria Teresa Ionta
    • Marina Pisano
    • Francesco Tanda
    • Antonio Cossu
    • Giuseppe Palmieri
  • View Affiliations

  • Published online on: January 28, 2014     https://doi.org/10.3892/ol.2014.1834
  • Pages: 948-952
Metrics: Total Views: 0 (Spandidos Publications: | PMC Statistics: )
Total PDF Downloads: 0 (Spandidos Publications: | PMC Statistics: )


Abstract

Germline mutations in BRCA1 or BRCA2 genes have been demonstrated to increase the risk of developing breast cancer. Among the prognostic factors currently used in clinical practice, the disease stage and the receptor status play a crucial role in the management of breast carcinoma. Triple‑negative breast cancer (TNBC) has been classified as a disease subgroup that is negative for oestrogen, progesterone and HER2 receptor expression, and presents a poor prognosis. The present study investigated the correlation between BRCA1/2 mutations and TNBC status in a large series (n=726) of breast cancer patients from Sardinia. The BRCA mutation screening was performed on genomic DNA from peripheral blood samples by denaturing high‑performance liquid chromatography analysis and automated DNA sequencing. Overall, 21/726 (2.9%) patients carried a germline mutation in BRCA1 or BRCA2. The TNBC phenotype was significantly associated with the BRCA1 mutations (P<0.001), whereas no association was found with the BRCA2 mutations (P=0.837). With respect to patient origin within Sardinia, a significant inverse distribution of mutations was found; BRCA1 and BRCA2 mutations represented 86 and 93% of the mutated cases in Southern and Middle‑Northern Sardinia, respectively (P<0.001). Patients from the geographical area with BRCA1 mutation prevalence presented a TNBC incidence much higher than that observed in cases from the area with BRCA2 mutation prevalence (12 vs. 4%, respectively; P=0.037). These findings further confirmed that the occurrence of TNBC is significantly associated with the BRCA1 mutation carrier status and that a different ‘genetic background’ may have a phenotypic impact in the onset of breast cancer.
View Figures
View References

Related Articles

Journal Cover

2014-April
Volume 7 Issue 4

Print ISSN: 1792-1074
Online ISSN:1792-1082

Sign up for eToc alerts

Recommend to Library

Copy and paste a formatted citation
x
Spandidos Publications style
Palomba G, Budroni M, Olmeo N, Atzori F, Ionta MT, Pisano M, Tanda F, Cossu A and Palmieri G: Triple‑negative breast cancer frequency and type of BRCA mutation: Clues from Sardinia. Oncol Lett 7: 948-952, 2014
APA
Palomba, G., Budroni, M., Olmeo, N., Atzori, F., Ionta, M.T., Pisano, M. ... Palmieri, G. (2014). Triple‑negative breast cancer frequency and type of BRCA mutation: Clues from Sardinia. Oncology Letters, 7, 948-952. https://doi.org/10.3892/ol.2014.1834
MLA
Palomba, G., Budroni, M., Olmeo, N., Atzori, F., Ionta, M. T., Pisano, M., Tanda, F., Cossu, A., Palmieri, G."Triple‑negative breast cancer frequency and type of BRCA mutation: Clues from Sardinia". Oncology Letters 7.4 (2014): 948-952.
Chicago
Palomba, G., Budroni, M., Olmeo, N., Atzori, F., Ionta, M. T., Pisano, M., Tanda, F., Cossu, A., Palmieri, G."Triple‑negative breast cancer frequency and type of BRCA mutation: Clues from Sardinia". Oncology Letters 7, no. 4 (2014): 948-952. https://doi.org/10.3892/ol.2014.1834