- Research article
- Open Access
Triple-negative breast cancer and PTEN (phosphatase and tensin homologue)loss are predictors of BRCA1 germline mutations in women with early-onset and familial breast cancer, but not in women with isolated late-onset breast cancer
Breast Cancer Research volume 14, Article number: R142 (2012)
Given that breast cancers in germline BRCA1 carriers are predominantly estrogen-negative and triple-negative, it has been suggested that women diagnosed with triple-negative breast cancer (TNBC) younger than 50 years should be offered BRCA1 testing, regardless of family cancer characteristics. However, the predictive value of triple-negative breast cancer, when taken in the context of personal and family cancer characteristics, is unknown. The aim of this study was to determine whether TNBC is a predictor of germline BRCA1 mutations, in the context of multiple predictive factors.
Germline mutations in BRCA1 and BRCA2 were analyzed by Sanger sequencing and multiple ligation-dependent probe amplification (MLPA) analysis in 431 women from the Malaysian Breast Cancer Genetic Study, including 110 women with TNBC. Logistic regression was used to identify and to estimate the predictive strength of major determinants. Estrogen receptor (ER) and phosphatase and tensin homologue (PTEN) status were assessed and included in a modified Manchester scoring method.
Our study in an Asian series of TNBC patients demonstrated that 27 (24.5%) of 110 patients have germline mutations in BRCA1 (23 of 110) and BRCA2 (four of 110). We found that among women diagnosed with breast cancer aged 36 to 50 years but with no family history of breast or ovarian cancer, the prevalence of BRCA1 and BRCA2 mutations was similar in TNBC (8.5%) and non-TNBC patients (6.7%). By contrast, in women diagnosed with breast cancer, younger than 35 years, with no family history of these cancers, and in women with a family history of breast cancer, the prevalence of mutations was higher in TNBC compared with non-TNBC (28.0% and 9.9%; P = 0.045; and 42.1% and 14.2%; P < 0.0001, respectively]. Finally, we found that incorporation of estrogen-receptor and TNBC status improves the sensitivity of the Manchester Scoring method (42.9% to 64.3%), and furthermore, incorporation of PTEN status further improves sensitivity (42.9% to 85.7%).
We found that TNBC is an important criterion for highlighting women who may benefit from genetic testing, but that this may be most useful for women with early-onset breast cancer (35 years or younger) or with a family history of cancers. Furthermore, addition of TNBC and PTEN status improves the sensitivity of the Manchester scoring method and may be particularly important in the Asian context, where risk-assessment models underestimate the number of mutation carriers.
Discovery of the breast cancer-predisposition genes BRCA1 and BRCA2 has enabled us to identify carriers accurately, to target the reduction of risk of breast and ovarian cancers in carriers, and to develop a new generation of targeted therapies (PARP inhibitors) . However, given that deleterious mutations in these genes account for only 1% to 4% of all breast cancer cases across different populations  and that genetic testing and genetic counseling have hitherto been relatively expensive, genetic testing for BRCA1 and BRCA2 has typically been offered only in clinical genetics settings to women who have early-onset breast cancer, and/or to individuals with significant family history of breast and ovarian, or other BRCA-related cancers.
Recently, it was suggested that screening women with early-onset triple-negative breast cancer (TNBC) may be a cost-effective method with which to identify BRCA1 mutation carriers in Caucasian women [3–5]. This is because, in the majority of BRCA1 carriers, breast tumors have distinctive morphologic features and immunohistochemical phenotypes characteristic of basal-like breast cancers, including negative expression of the estrogen receptor, high expression of basal markers, such as basal cytokeratins CK5/6 and CK14, and loss of tumor-suppressor PTEN [6–8]. Moreover, molecular gene-expression profiling of BRCA1 tumors showed that the tumors have significant similarities with the basal-like subtype of breast cancer . Up to 50% of women diagnosed with breast cancer, younger than 50 years, and women who have a family cancer history may have mutations in BRCA1 or BRCA2 . However, it is notable that although more than 10% women in whom an isolated TNBC develops at younger than 40 years old may have a mutation in BRCA1 [3–5], insufficient evidence exists for those aged 41 to 50 years, with no family history of breast or ovarian cancer .
The purpose of this study was to determine whether TNBC is an independent criterion for stratifying women with an increased risk of having a BRCA1 mutation and to determine whether the addition of immunohistologic features of basal-like breast cancers helps to define a subset of women who are likely to have germline mutations in BRCA1.
Materials and methods
MyBrCa Breast cancer cohort
The recruitment of breast cancer patients into the Malaysian Breast Cancer Genetic Study (MyBrCa) started in January 2003 at the University Malaya Medical Centre in Kuala Lumpur. All were histopathology-proven breast carcinomas. Histomorphologic and biomarker parameters were retrieved from the histopathology reports. Blood, demographic, and family-history data were collected from breast cancer patients who consented to participate in this study. This study was approved by the ethics committee of University Malaya Medical Centre.
Analysis of BRCA1 and BRCA2
From January 2003 to February 2012, 1,454 breast cancer patients were recruited into the MyBrCa study. Germline DNA samples were screened for BRCA1 and BRCA2 mutations for all women with (a) early-onset breast cancer (≤35 years of age) (35 with and 96 without family history of breast and ovarian cancer); (b) family history of breast or ovarian cancer in first- and second-degree relatives (193 women); or (c) isolated triple-negative breast cancer diagnosed at between 36 and 50 years old in the absence of family history (47 women). In addition, of the 432 women who were diagnosed aged 36 to 50 years with non-TNBC, 60 women with the highest risk were analyzed (bilateral breast cancer, breast and ovarian cancer in the index patient, family history of breast and ovarian cancer in third-degree or isolated breast cancer (≤45 years of age)). Mutation detection for germline BRCA1 and BRCA2 mutations was conducted by using direct DNA sequencing and multiple ligation-dependent probe amplification (MLPA), as previously described [12, 13].
For this cohort, patients were classified as having TNBC when we found <10% ER-, <10% PR-, and 0 or ≤2+ HER2 staining with immunohistochemistry. HER2 was not routinely tested for in all patients prior to 2006, and therefore, in 259 patients, HER2 status was unavailable. Of the 110 women for whom germline BRCA1 and BRCA2 mutations were analyzed, adequate archived paraffinized invasive tumor tissue for evaluation was available from 32 index patients and two relatives. All cases were tested with immunohistochemistry for cytokeratin 5/6 (D5/16B4; Dako Ltd.), cytokeratin 14 (LL02; Novocastra Labs), and PTEN (6H2.1; Dako). Cytokeratin 5/6 or cytokeratin 14 was defined as positive if >10% of invasive tumor cells showed cytoplasmic staining , and PTEN was defined as negative if PTEN staining was undetectable in tumor cells in contrast to adjacent normal stromal cells [6–8]. Description of other pathologic features was conducted as previously described .
Unconditional multiple linear logistic regression was used to model the probability that the proband was a mutation carrier as a function of her personal and family history and age at diagnosis, as described in .
Manchester score analysis
Manchester score was calculated as previously described . In brief, this system assigns scores depending on the type of cancer and age at diagnosis and developed such that a score of 15 was equivalent to a 10% chance of identifying a BRCA1 or BRCA2 mutation. The modified method [17–19] includes upward adjustments for TNBC (+4), estrogen-negative (+1), and high-grade invasive cancers (+2), and downward adjustments for human epidermal growth factor receptor 2 (HER2)-positive (-4) or estrogen-receptor positive (-1), lobular (-2), and low-grade noninvasive cancers (-2). For individuals in whom tumor tissue was available for PTEN staining, upward (+1) and downward (-1) adjustments were made for the absence or presence of PTEN staining, respectively.
Prevalence of BRCA1 and BRCA2 germline mutations is higher among subsets of women with TNBC compared with non-TNBC
Of the 1,454 breast cancer patients in the MyBrCa Study, 177 (12.2%) had TNBC based on pathology reports. Of these 177 women, 50 older than 50 years developed breast cancer and did not have any family history of breast or ovarian cancer in first- or second-degree relatives and were therefore excluded from the study. Of the remaining 127 women, 63 had already been analyzed because of family history of either breast and/or ovarian cancer (38 individuals, 13 BRCA1 and three BRCA2 carriers, mutation prevalence, 42.1%) or early-onset breast cancer (25 individuals, seven BRCA1 and no BRCA2 carriers; mutation prevalence, 28.0%]. Of the remaining 64 women diagnosed at ages 36 through 50 years, but with no family history of breast or ovarian cancer, 47 women were screened for germline mutations in BRCA1 and BRCA2 genes, and three BRCA1 and one BRCA2 carriers were identified (mutation prevalence, 8.5%). Overall, of the 110 women who developed TNBC and were analyzed (63 with and 47 without family history of breast and ovarian cancers), 23 BRCA1 and 4 BRCA2 carriers were identified, giving a mutation prevalence of 24.5% (Table 1).
In total, 321 women with non-TNBC were analyzed. This included all women with a family history of breast and/or ovarian cancer (190 individuals, 10 BRCA1 and 17 BRCA2 carriers, mutation prevalence 14.2%) and women diagnosed at 35 years or younger with no family history of breast and ovarian cancer (71 individuals, three BRCA1 and four BRCA2 carriers; mutation prevalence, 9.9% (Table 2)). In addition, of the 432 women who were diagnosed aged 36 through 50 years with non-TNBC, 60 women with the highest risk were analyzed (bilateral breast cancer, breast and ovarian cancer in the index patient, family history of breast and ovarian cancer in third degree or isolated breast cancer (aged 45 years or younger)). Of these 60 women, one BRCA1 and three BRCA2 carriers were found [mutation prevalence, 6.7%]. Overall, of the 321 non-TNBC women analyzed, 14 BRCA1 and 24 BRCA2 carriers were identified, giving a mutation prevalence of 11.8%.
We compared the prevalence of BRCA1 and BRCA2 mutations in the women who developed TNBC and non-TNBC. Of the women with low familial risk of breast and ovarian cancer (diagnosed 36 to 50 with no family history of breast or ovarian cancer], 6.4% and 1.7% of women with TNBC and non-TNBC were found to be BRCA1 carriers, respectively, whereas 2.1% and 5.0% were BRCA2 carriers. Overall, 8.5% of women with TNBC and 6.7% of women with non-TNBC were found to have germline BRCA1 or BRCA2 mutations. This suggests that, regardless of the TNBC status, in the absence of family history of breast or ovarian cancer in this age group, a low (<10%) probability exists of having a BRCA1 or BRCA2 mutation.
By contrast, in two other groups of women, a significantly higher prevalence of BRCA1 mutations was found in women who developed TNBC versus non-TNBC. First, of the women in whom breast cancer developed at 35 years or younger, 28.0% of women with TNBC were BRCA1 or BRCA2 carriers compared with only 9.9% among those who developed non-TNBC (P = 0.045). Notably, all 28.0% of women diagnosed with TNBC at younger than 35 years were BRCA1 carriers, compared with 4.2% BRCA1 and 5.6% BRCA2 among women diagnosed with non-TNBC.
Second, of women who had a family history of breast and/or ovarian cancer, 42.1% of women with TNBC were BRCA1 or BRCA2 carriers compared with 14.2% of those with non-TNBC (P = < 0.0001). This is largely because of a difference in prevalence of BRCA1 mutations in TNBC compared with non-TNBC (34.2% compared with 5.3%; P = < 0.0001), as no significant difference occurred in the prevalence of BRCA2 in both subsets of women (7.9% compared with 8.9%; P = 1.00). Notably, no significant difference was noted in average age at onset of breast cancer in the index patient, or the mean number of first-degree relatives of women in whom TNBC developed compared with the non-TNBC (seven relatives), but the mean number of affected relatives in the non-TNBC group was higher than that in the TNBC group (0.8 compared with 0.6; P = 0.003). This suggests that the higher prevalence of BRCA1 mutations in the women in whom TNBC developed compared with women in whom non-TNBC developed is not due to a difference in the age at onset or strength of family history. Taken together, the results suggest that early onset and familial breast cancer patients in whom TNBC develops are more likely to have mutations in the BRCA1 genes compared with those in whom non-TNBC develops (24.5% versus 11.8%; P = 0.001).
In addition, in this cohort, a marked difference appears in prevalence of BRCA1 and BRCA2 in the TNBC and non-TNBC patients. TNBC patients are more likely to have BRCA1 than BRCA2 mutations (20.9% and 4.4%; p < 0.0001), whereas no statistically significant difference is present in BRCA1 and BRCA2 mutations in non-TNBC patients (3.6% and 7.5%, respectively; P = 0.158).
Logistic regression analyses
Given the possible confounding between the age of diagnosis, subtype of breast cancer, and family history of cancer, it has been demonstrated that the predictive effects of factors should be based on an analysis that takes into account all factors simultaneously . By using binary logistic regression analysis, we found that age at diagnosis of breast cancer, having any family history of breast or ovarian cancer, and having triple-negative breast cancer were associated with a 2.6-fold (confidence interval (CI), 1.4 to 4.8; P < 0.003), 3.5-fold (CI, 1.9 to 6.8; P < 0.0001), and 3.5-fold (CI, 1.91 to 6.3; P < 0.0001) increase in risk of being a BRCA1 or BRCA2 carrier, respectively. No evidence of interaction effects between these factors was seen. With multiple linear logistic regression analysis, the strongest predictors of mutation status were breast cancer in the proband if age at diagnosis was younger than 35 years (P = 0.043), with bilateral breast cancer (P = 0.025), with triple-negative breast cancer (P < 0.0001), with breast cancer in a first-degree relative if age at diagnosis was younger than 60 years (P < 0.01), or ovarian cancer was present in a first- or second-degree relative (P < 0.025) (Table 3).
The probability that a proband with a given set of personal and family characteristics is a mutation carrier can be estimated from the model fit shown in Table 4. Starting with the log odds score of θ (the baseline coefficient), add the respective regression coefficient (β) for each personal characteristic and the respective regression for each family characteristic multiplied by the number of affected relatives. In this model, an overall score of -1.5 is equivalent to a 15% probability of being a BRCA1 or BRCA2 carrier. Notably, the overall scores for women with isolated TNBC who were diagnosed aged ≤35 years old, 36 to 39 years old, or 40 to 49 years old, are -1.1, -1.6, and -2.1, respectively, which correlates with a 29%, 14%, and 9% probability of being a BRCA1 or BRCA2 carrier. The overall scores for women with isolated non-TNBC who were diagnosed at younger than 35 years, 36 to 39 years old, and 40 to 49 years old, are -2.4, -2.9, and -3.4, respectively, which correlates with a 9%, 4%, and 4% probability of being a BRCA1 or BRCA2 carrier. These results show that women with isolated TNBC have a higher probability of being carriers compared with women with isolated non-TNBC and that, of the women with isolated breast cancers, only women with isolated TNBC diagnosed at younger than 40 years have a greater than 10% probability of having germline mutations in BRCA1 or BRCA2.
Pathologic features of BRCA1 and non-BRCA1 triple-negative breast cancer
We analyzed the pathology reports of BRCA1 carriers and compared them with those in BRCA2 and non-BRCA carriers. Of the 31 BRCA1 index carriers and affected relatives where pathology reports were available, 26 (83.9%) developed TNBC. By contrast, of the 270 BRCA2 carriers and non-BRCA carriers, 88 (32.6%) developed TNBC.
Of the 110 TNBC patients included in this study and for whom germline status of BRCA1 and BRCA2 has been characterized (see earlier), 34 had adequate invasive tumor tissue for evaluation. Slides were cut and immunostained for several markers that have been reported to be useful in defining the basal-like phenotype, including basal cytokeratins CK5/6, CK14, and PTEN. Although some higher grade were present, higher basal cytokeratin, loss of PTEN, high grade of pleomorphism, presence of pushing margins, solid sheets, necrosis, and mitosis in BRCA1 carriers compared with non-BRCA1 carriers, these differences were not statistically significant (see Additional file 1).
Inclusion of pathologic features in Manchester scores
To determine whether the addition of pathologic features can define a subset of women who are likely to have germline mutations in BRCA1 or BRCA2, we calculated the Manchester score for each individual based on the original Manchester score  and on the updated Manchester score where pathology was included . Upward adjustments in BRCA1 mutation-prediction scores were made for grade 3 ductal cancers, estrogen receptor (ER), and triple-negative tumors, and downward adjustments in the score were made for grade 1 tumors, lobular cancer, ductal or lobular carcinoma in situ, noninvasive breast cancer, and ER/HER2 positivity, as described previously .
Of the 431 women in this study, 86 were excluded because pathology reports were incomplete. Without adjustment, 72 of 345 women had a Manchester score of ≥15, and this included only 12 of the 28 BRCA1 carriers (sensitivity, 42.9%; specificity, 81.1%; PPV, 16.7%). With the adjustment, 82 of the 345 women had a Manchester score of ≥15, and this included 18 of the 28 BRCA1 carriers (sensitivity, 64.3%; specificity, 79.8%; PPV, 22.0%) (Table 5). These results show that adjustment in this cohort resulted in 14% increase in the number of tests (72 to 82) and 21% increase in sensitivity (43% to 64%).
In addition, given that PTEN loss was associated with BRCA1 germline mutations , we made a further upward adjustment for PTEN loss (+1 point) for all patients for whom PTEN status was available. Without adjustment, five of 26 women had a >10% probability of BRCA1 and BRCA2 mutations, and this included only three of the seven BRCA1 carriers (sensitivity, 42.9%; specificity, 89.5%; PPV, 60.0%). With the adjustment for PTEN loss, 10 of the 26 women had a Manchester score ≥15, and this included six of the seven BRCA1 carriers (sensitivity, 85.7%; specificity, 78.9%; PPV, 60.0%; Table 5). Although PTEN results were available for only a small subset of patients, these results suggest that upward adjustment for PTEN may aid the identification of BRCA1 carriers.
Our study in an Asian series of triple-negative breast cancer patients demonstrated that up to 24.5% (27 of 110) women have germline mutations in BRCA1 (23 of 110) and BRCA2 (four of 110), and that the addition of negative estrogen-receptor status and PTEN loss improves the sensitivity of the Manchester Scoring method in our Asian cohort.
The results in this study are consistent with that in other cohorts of triple-negative breast cancer patients, in whom 11% to 39% have germline mutations in BRCA1 and BRCA2 [3, 6, 20–23], and cohorts of estrogen-receptor-negative breast cancer patients, of whom 24% to 29% have germline mutations in BRCA1 and BRCA2 [4, 6, 24, 25]. A recent single-institution study showed that 50% of high-risk patients with TNBC had mutations in BRCA1/2, but notably, 76% of this cohort had a family history of breast cancer . For all of these series and for our study, BRCA1 mutations are more common than BRCA2 mutations.
Cost-effectiveness analyses have suggested that mutation testing for all TNBC patients younger than 50 years old may be a cost-effective approach, assuming that 10% to 25% of these patients have BRCA1 or BRCA2 mutations . However, we find that although TNBC is associated with an increased prevalence of BRCA1 and BRCA2 mutations among those younger than 35 years old (28.0% in TNBC versus 9.9% in non-TNBC; P = 0.045], TNBC is not associated with an increased prevalence of mutations among those aged 36 to 50 years without a family history of breast or ovarian cancer (BRCA prevalence of 8.5% and 6.7%, respectively). This may be because BRCA1 is a high-penetrance gene and is associated with both early-onset disease and multiple affected family members, and therefore, in the absence of these features, a low prevalence of BRCA1 mutations is found, even in TNBC. Further studies with larger population-based datasets are needed to determine the prevalence of BRCA1 and BRCA2 mutations and the cost-effectiveness of testing women diagnosed with isolated breast cancer, aged 40 to 49 years old.
We find that the prevalence of BRCA1 mutations is higher in TNBC compared with non-TNBC in women in whom early-onset breast cancer develops and in women with a family history of breast and ovarian cancer. This effect is largely due to a difference in prevalence of BRCA1 mutations and is consistent with the observation that the majority of BRCA1 carriers develop early-onset triple-negative basal-like breast tumors that have distinctive morphologic and immunohistochemical characteristics [6–8]. Intriguingly, the significant proportion of TNBC patients who have BRCA1 germline mutations in these two subgroups of patients (28.0% and 34.2%) suggests that mutation in BRCA1 is a key driver of the development of TNBC. This could be due to the roles of BRCA1 in determining cell fate of luminal progenitor cells , its effect on transcriptional regulation of ER-gene expression , its effect on regulation of mi155 , or a combination of these.
Taken together, we suggest that TNBC status may be helpful in stratifying women with a moderate risk of having BRCA1 mutations (for example, a weak family history or isolated case of early-onset breast cancer), but may have limited utility in the absence of such features (for example, women with a single case of TNBC aged 40 to 50 years old).
Finally, we find that addition of negative estrogen receptor and TNBC status improves the sensitivity and specificity of the Manchester Scoring method in our cohort and that addition of PTEN loss further improves the sensitivity of the method. PTEN loss is highly associated with BRCA1 breast cancers (28 (82.4%) of 34 of tumor samples from BRCA1 carriers showed the loss of PTEN by immunohistochemistry) and can result from gene rearrangements involving DNA double-strand breaks, intragenic inversions on insertions, homozygous deletions, and focalized CNIs . However, given that the data on PTEN loss were available on only a small subset of patients, this result requires further validation in a larger cohort of patients. We believe that methods for stratifying the likelihood of carrying a BRCA1 and BRCA2 mutation that is independent of family history are important, particularly in the Asian context, because the familial and social stigma associated with cancer makes accurate family-history reporting challenging .
In previous studies and in our cohort of TNBC, a significant proportion of women have germline BRCA1 mutations. Our study shows that among women with early-onset breast cancer (≤35 years old) and with a family history of breast cancer, a higher prevalence of BRCA1 mutations is present in women with TNBC compared with women with non-TNBC. However, no difference in prevalence of BRCA1 and BRCA2 mutations is noted among women who develop isolated breast cancer aged 36 to 50 (7% to 8% prevalence in both TNBC and non-TNBC). Our study suggests that the current clinical recommendations of offering BRCA1 and BRCA2 genetic testing, even to women with isolated TNBC younger than 60 years, warrants further analysis.
- BRCA1 :
breast cancer 1 gene
- BRCA2 :
breast cancer 2 gene
DNA copy number increase
human epidermal growth factor receptor 2
Malaysian Breast Cancer Genetic Study
National Comprehensive Cancer Network
phosphatase and tensin homologue
triple-negative breast cancer.
Rehman FL, Lord CJ, Ashworth A: Synthetic lethal approaches to breast cancer therapy. Nat Rev Clin Oncol. 2010, 7: 718-724. 10.1038/nrclinonc.2010.172.
Kurian AW: BRCA1 and BRCA2 mutations across race and ethnicity: distribution and clinical implications. Curr Opin Obstet Gynecol. 2010, 22: 72-78. 10.1097/GCO.0b013e328332dca3.
Young SR, Pilarski RT, Donenberg T, Shapiro C, Hammond LS, Miller J, Brooks KA, Cohen S, Tenenholz B, Desai D, Zandvakili I, Royer R, Li S, Narod SA: The prevalence of BRCA1 mutations among young women with triple-negative breast cancer. BMC Cancer. 2009, 9: 86-10.1186/1471-2407-9-86.
Chang J, Hilsenbeck SG, Sng JH, Wong J, Ragu GC: Pathological features and BRCA1 mutation screening in premenopausal breast cancer patients. Clin Cancer Res. 2001, 7: 1739-1742.
Kwon JS, Gutierrez-Barrera AM, Young D, Sun CC, Daniels MS, Lu KH, Arun B: Expanding the criteria for BRCA mutation testing in breast cancer survivors. J Clin Oncol. 2010, 28: 4214-4220. 10.1200/JCO.2010.28.0719.
Foulkes WD, Stefansson IM, Chappuis PO, Begin LR, Goffin JR, Wong N, Trudel M, Akslen LA: Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer. J Natl Cancer Inst. 2003, 95: 1482-1485. 10.1093/jnci/djg050.
Lakhani SR, Reis-Filho JS, Fulford L, Penault-Llorca F, van der Vijver M, Parry S, Bishop T, Benitez J, Rivas C, Bignon YJ, Chang-Claude J, Hamann U, Cornelisse CJ, Devilee P, Beckmann MW, Nestle-Krämling C, Daly PA, Haites N, Varley J, Lalloo F, Evans G, Maugard C, Meijers-Heijboer H, Klijn JG, Olah E, Gusterson BA, Pilotti S, Radice P, Scherneck S, Sobol H, et al: Prediction of BRCA1 status in patients with breast cancer using estrogen receptor and basal phenotype. Clin Cancer Res. 2005, 11: 5175-5180. 10.1158/1078-0432.CCR-04-2424.
Saal LH, Gruvberger-Saal SK, Persson C, Lövgren K, Jumppanen M, Staaf J, Jönsson G, Pires MM, Maurer M, Holm K, Koujak S, Subramaniyam S, Vallon-Christersson J, Olsson H, Su T, Memeo L, Ludwig T, Ethier SP, Krogh M, Szabolcs M, Murty VV, Isola J, Hibshoosh H, Parsons R, Borg A: Recurrent gross mutations of the PTEN tumor suppressor gene in breast cancers with deficient DSB repair. Nat Genet. 2008, 40: 102-107. 10.1038/ng.2007.39.
Sorlie T, Perou CM, Tibshirani R, Aas T, Geisler S, Johnsen H, Hastie T, Eisen MB, van de Rijn M, Jeffrey SS, Thorsen T, Quist H, Matese JC, Brown PO, Botstein D, Lonning PE, Borresen-Dale AL: Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications. Proc Natl Acad Sci USA. 2001, 98: 10869-10874. 10.1073/pnas.191367098.
Bayraktar S, Gutierrez-Barrera AM, Liu D, Tasbas T, Akar U, Litton JK, Lin E, Albarracin CT, Meric-Bernstam F, Gonzalez-Angulo AM, Hortobagyi GN, Arun BK: Outcome of triple-negative breast cancer in patients with or without deleterious BRCA mutations. Breast Cancer Res Treat. 2011, 130: 145-153. 10.1007/s10549-011-1711-z.
Evans DG, Howell A, Ward D, Lalloo F, Jones JL, Eccles DM: Prevalence of BRCA1 and BRCA2 mutations in triple negative breast cancer. J Med Genet. 2011, 48: 520-522. 10.1136/jmedgenet-2011-100006.
Thirthagiri E, Lee SY, Kang P, Lee DS, Toh GT, Selamat S, Yoon SY, Taib NA, Thong MK, Yip CH, Teo SH: Evaluation of BRCA1 and BRCA2 mutations and risk-prediction models in a typical Asian country (Malaysia) with a relatively low incidence of breast cancer. Breast Cancer Res. 2008, 10: R59-10.1186/bcr2118.
Toh GT, Kang P, Lee SS, Lee DS, Lee SY, Selamat S, Mohd Taib NA, Yoon SY, Yip CH, Teo SH: BRCA1 and BRCA2 germline mutations in Malaysian women with early-onset breast cancer without a family history. PLoS One. 2008, 3: e2024-10.1371/journal.pone.0002024.
Lakhani SR, Jacquemier J, Sloane JP, Gusterson BA, Anderson TJ, van de Vijver MJ, Farid LM, Venter D, Antoniou A, Storfer-Isser A, Smyth E, Steel CM, Haites N, Scott RJ, Goldgar D, Neuhausen S, Daly PA, Ormiston W, McManus R, Scherneck S, Ponder BA, Ford D, Peto J, Stoppa-Lyonnet D, Bignon YJ, Struewing JP, Spurr NK, Bishop DT, Klijn JG, Devilee P, et al: Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations. J Natl Cancer Inst. 1998, 90: 1138-1145. 10.1093/jnci/90.15.1138.
Apicella C, Andrews L, Hodgson SV, Fisher SA, Lewis CM, Solomon E, Tucker K, Friedlander M, Bankier A, Southey MC, Venter DJ, Hopper JL: Log odds of carrying an Ancestral Mutation in BRCA1 or BRCA2 for a Defined personal and family history in an Ashkenazi Jewish woman (LAMBDA). Breast Cancer Res. 2003, 5: R206-216. 10.1186/bcr644.
Evans DG, Lalloo F, Wallace A, Rahman N: Update on the Manchester Scoring System for BRCA1 and BRCA2 testing. J Med Genet. 2005, 42: e39-10.1136/jmg.2005.031989.
Mavaddat N, Rebbeck TR, Lakhani SR, Easton DF, Antoniou AC: Incorporating tumour pathology information into breast cancer risk prediction algorithms. Breast Cancer Res. 2010, 12: R28-10.1186/bcr2576.
Evans DG, Lalloo F, Cramer A, Jones EA, Knox F, Amir E, Howell A: Addition of pathology and biomarker information significantly improves the performance of the Manchester scoring system for BRCA1 and BRCA2 testing. J Med Genet. 2009, 46: 811-817. 10.1136/jmg.2009.067850.
James PA, Doherty R, Harris M, Mukesh BN, Milner A, Young MA, Scott C: Optimal selection of individuals for BRCA mutation testing: a comparison of available methods. J Clin Oncol. 2006, 24: 707-715. 10.1200/JCO.2005.01.9737.
Haffty BG, Silber A, Matloff E, Chung J, Lannin D: Racial differences in the incidence of BRCA1 and BRCA2 mutations in a cohort of early onset breast cancer patients: African American compared to white women. J Med Genet. 2006, 43: 133-137.
Atchley DP, Albarracin CT, Lopez A, Valero V, Amos CI, Gonzalez-Angulo AM, Hortobagyi GN, Arun BK: Clinical and pathologic characteristics of patients with BRCA-positive and BRCA-negative breast cancer. J Clin Oncol. 2008, 26: 4282-4288. 10.1200/JCO.2008.16.6231.
Gonzalez-Angulo AM, Timms KM, Liu S, Chen H, Litton JK, Potter J, Lanchbury JS, Stemke-Hale K, Hennessy BT, Arun BK, Hortobagyi GN, Do KA, Mills GB, Meric-Bernstam F: Incidence and outcome of BRCA mutations in unselected patients with triple receptor-negative breast cancer. Clin Cancer Res. 2011, 17: 1082-1089. 10.1158/1078-0432.CCR-10-2560.
Comen E, Davids M, Kirchhoff T, Hudis C, Offit K, Robson M: Relative contributions of BRCA1 and BRCA2 mutations to "triple-negative" breast cancer in Ashkenazi women. Breast Cancer Res Treat. 2011, 129: 185-190. 10.1007/s10549-011-1433-2.
Karp SE, Tonin PN, Begin LR, Martinez JJ, Zhang JC, Pollak MN, Foulkes WD: Influence of BRCA1 mutations on nuclear grade and estrogen receptor status of breast carcinoma in Ashkenazi Jewish women. Cancer. 1997, 80: 435-441. 10.1002/(SICI)1097-0142(19970801)80:3<435::AID-CNCR11>3.0.CO;2-Y.
Lidereau R, Eisinger F, Champeme MH, Nogues C, Bieche I, Birnbaum D, Pallud C, Jacquemier J, Sobol H: Major improvement in the efficacy of BRCA1 mutation screening using morphoclinical features of breast cancer. Cancer Res. 2000, 60: 1206-1210.
Lim E, Vaillant F, Wu D, Forrest NC, Pal B, Hart AH, Asselin-Labat ML, Gyorki DE, Ward T, Partanen A, Feleppa F, Huschtscha LI, Thorne HJ, kConFab, Fox SB, Yan M, French JD, Brown MA, Smyth GK, Visvader JE, Lindeman GJ: Aberrant luminal progenitors as the candidate target population for basal tumor development in BRCA1 mutation carriers. Nat Med. 2009, 15: 907-913. 10.1038/nm.2000.
Chang S, Wang RH, Akagi K, Kim KA, Martin BK, Cavallone L, kConFab, Haines DC, Basik M, Mai P, Poggi E, Isaacs C, Looi LM, Mun KS, Greene MH, Byers SW, Teo SH, Deng CX, Sharan SK: Tumor suppressor BRCA1 epigenetically controls oncogenic microRNA-155. Nat Med. 2011, 17: 1275-1282. 10.1038/nm.2459.
Yoon SY, Thong MK, Taib NA, Yip CH, Teo SH: Genetic counseling for patients and families with hereditary breast and ovarian cancer in a developing Asian country: an observational descriptive study. Family Cancer. 2011, 10: 199-205. 10.1007/s10689-011-9420-7.
We thank participants and their families for taking part in this study; Eswary Thirthagiri, Shivaani Mariapun, Peter Kang, Daphne Lee, Kavitta Sivanandan, Kang In Nee, and Tomica Ambang for assistance with DNA preparation, retrieval of pathology data, calculation of Manchester score, and helpful discussions; and Thong Meow Keong and Yoon Sook-Yee for genetic counseling of BRCA carriers. This study was funded by research grants from the Malaysian Ministry of Science, Technology and Innovation, Ministry of Higher Education University Malaya (UM.C/HlR/MOHE/06), and Cancer Research Initiatives Foundation.
The authors declare that they have no competing interests.
PSY carried out the genetic analyses. LLM, AR, and SD conducted the pathological analyses, and NH conducted the statistical analyses. NAMT and YCH recruited patients and collected clinical data. PSY and TSH conceived the study and drafted the manuscript. All authors read and approved the final manuscript.
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Phuah, S., Looi, L., Hassan, N. et al. Triple-negative breast cancer and PTEN (phosphatase and tensin homologue)loss are predictors of BRCA1 germline mutations in women with early-onset and familial breast cancer, but not in women with isolated late-onset breast cancer. Breast Cancer Res 14, R142 (2012). https://0-doi-org.brum.beds.ac.uk/10.1186/bcr3347
- Breast Cancer
- Ovarian Cancer
- Germline Mutation
- BRCA2 Mutation
- BRCA2 Carrier