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Genet Mol Biol. 2016 Apr-Jun; 39(2): 199–202.
Published online 2016 May 24. doi:  10.1590/1678-4685-GMB-2014-0343
PMCID: PMC4910548

Early-onset breast cancer patients in the South and Southeast of Brazil should be tested for the TP53 p.R337H mutation

Abstract

Germline TP53 mutations are associated with Li-Fraumeni syndrome (LFS), a disease that predisposes carriers to a wide variety of early onset tumors. In southern and southeastern Brazil, a high frequency of a germline TP53 mutation, p.R337H, was diagnosed in 0,3% of the population due to a founder effect. Carriers are at risk for developing cancer but the penetrance is lower than in typical DNA binding domain mutations. To date, only a few families were detected and diagnosis of carriers remains a challenge. Therefore, the inclusion of additional criteria to detect p.R337H carriers is necessary for the Brazilian population. We assessed the A.C. Camargo Cancer Center Oncogenetics Department database in search of common characteristics associated with p.R337H families that did not fulfill LFS/LFL clinical criteria. Among 42 p.R337H families, three did not meet any LFS/LFL criteria. All cases were young female patients with breast cancer diagnosed before age 45 and with no family history of LFS linked-cancers. Our results suggest that screening for the germline TP53 p.R337H mutation should be indicated, along with BRCA1 and BRCA2 genetic testing, for this group of patients, especially in the South and Southeast of Brazil.

Keywords: Breast cancer, Li-Fraumeni syndrome, p.R337H, TP53

Li-Fraumeni syndrome (LFS, OMIM #151623) is a rare autosomal dominant genetic disorder inherited by germline TP53 mutations (Malkin et al., 1990). Carriers are predisposed to the development of a wide variety of early onset tumors, especially to those denominated as LFS core tumors: premenopausal breast cancer, soft-tissue sarcoma (STS), central nervous system tumors (CNS), and adrenocortical carcinomas (ADR) (Li and Fraumeni, 1969a, b).

In order to identify at-risk families who carry these mutations, different criteria for clinical diagnosis have been established (Table 1). Since its publication, classical criteria have been modified due to the presence of families which, although not fulfilling the definition, were positive for germline TP53 mutations. This group of patients belongs to a variant form of LFS, named Li-Fraumeni-like (LFL), which is defined by either more inclusive parameters or additional criteria (Birch et al., 1994; Chompret et al., 2001; Eeles, 1995; Tinat et al., 2009).

Table 1
Clinical criteria for LFS diagnosis

Interestingly, a specific germline TP53 mutation (NC_000017.9: c.1010G > A; p.R337H) was reported as highly associated with LFS/LFL families in Brazil (Achatz et al., 2007). It is present in 0,3% of the local population from southern and southeastern regions of the country (Palmero et al., 2008; Custódio et al., 2013) due to a founder effect (Pinto et al., 2004; Garritano et al., 2010). One of the hypotheses to explain why this deleterious mutation has persisted is based on its relatively reduced penetrance, which confers a tumor risk of 30% before the age of 30, while lifetime cancer risk is similar to other TP53 mutations (Garritano et al., 2010). Thus, most carriers may have their children before developing cancer, spreading the mutation throughout generations. Also, the tumor profile among Brazilian carriers is similar to that of DNA-binding domain mutations found elsewhere in the world, but with some age difference and a higher risk for other types of tumors. In spite of its elevated prevalence, appropriate criteria to identify carriers, as well as guidelines to facilitate and direct genetic testing are still missing and, therefore, the number of carriers may be underestimated. Hence, our aim was to investigate the family history of p.R337H carriers who did not fulfill any of the LFS/LFL criteria, and define when individuals without criteria would benefit from testing for p.R337H.

This study is based on the A.C. Camargo Cancer Center Oncogenetics Department's database. The department has been following patients at high-risk for cancer development since 1999 and currently comprises 7,059 individuals from 607 families. For each family we obtained a detailed family history regarding tumor diagnosis and clinical data for both index patients and their relatives. Patients eligible for either TP53 sequencing or point-mutation directed genetic testing are also registered in this database. From 348 families tested for germline TP53 mutations, 42 were found to carry the p.R337H mutation.

Table 2 shows the number of families that fulfilled each of the LFS/LFL criteria. From the 42 families identified as p.R337H carriers, three did not meet any of the LFS/LFL criteria. According to their respective pedigrees (Figure 1), family Y0347 (Figure 1A) presented only two cases of maligancy: the proband with an invasive ductal carcinoma (IDC) diagnosed at the age 41 and her paternal uncle with prostate cancer at the age 60, which is not considered as an LFS-core tumor. Family Y0348 (Figure 1B) also presented cases of early-onset breast cancer; an IDC and a ductal carcinoma in situ (DCIS) diagnosed in the proband at the ages of 42 and 46, respectively, in addition to a breast cancer diagnosed in her mother at the age 61. Finally, the pedigree of family Y0349 (Figure 1C) includes a proband diagnosed with breast cancer at the age of 29 and cases of uterus and prostate cancers in her second- and third- degree relatives.

Table 2
Families carriers of the p.R337H mutation distributed according to different LFS criteria.
Figure 1
Pedigrees of the families affected by the germline TP53 p.R337H mutation. A) Family Y0347, B) Family Y0348, C) Family Y0349. The proband is indicated by an arrow; black symbol: patient affected by malignant tumor; yellow symbol: patient carrier of the ...

Altogether, we identified three different p.R337H families that did not fulfill any of the clinical criteria for LFS diagnosis. The main common observations in these families were the cases of breast cancer, diagnosed before age 45, irrespective of family history.

It has been suggested that women diagnosed with breast cancer before age 30, along with a family history of one or more core LFS cancers in a first- or second-degree relative should also be considered for TP53 genetic testing. Under this premise, Gonzalez et al. (2009) found a likelihood of 100% (5 of 5) individuals harboring a germline TP53 mutation. In contrast, the authors did not detect any mutation carrier in the group composed by 15 women diagnosed with invasive ductal carcinoma between the interval of 30-49 years and who did not have any core LFS tumor in the family history. Similar results were described later (Mouchawar et al., 2010), and the probability of identifying a germline TP53 mutation in women diagnosed with early onset breast cancer and who have a negative family history was defined as ranging from 5% to 8%, (McCuaig et al., 2012).

The three families detected in our study presented some features that should be carefully interpreted based on specific p.R337H characteristics. Different from the findings described by Gonzalez et al. (2009), two positive cases (Y0347T000 and Y0349T000) did not have any core LFS tumor in their first- or second-degree relatives. In addition, although the family Y0348 includes two cases of breast cancer, it did not meet any of the LFS criteria due to the relatively older age at tumor diagnosis of the proband's mother. These particularities could be consequences of the low penetrance presented by the p.R337H mutation, especially before the age of 30 (Garritano et al., 2010), which raises the possibility of later-than-expected ages at cancer development when compared to those described in currently applied LFS clinical criteria. Therefore, this might be a plausible explanation for both the absence of other affected individuals in the pedigree, as well as a slightly older age at cancer onset.

The indication of simultaneous genetic testing for BRCA1/BRCA 2 and TP53 has been proposed especially for women with breast cancer diagnosed before age 35 who have a family history of LFS-linked cancers (Lee et al., 2012). Conversely, Tinat et al. (2009) suggested TP53 testing only for women diagnosed with early onset breast cancer who are negative for mutations in BRCA1 and BRCA2, irrespective of family history. Nonetheless, the authors state that it should be avoided in those who do not present a family history of cancer or multiple primary tumors, mainly due to the low estimated prevalence of positive cases in this category (less than 5%) and the psychosocial burden induced by a TP53 genetic testing. In accordance with our observations, Gomes et al. (2012) described two p.R337H carriers diagnosed with breast cancer before the age 40 in an unselected breast cancer-cohort with 390 participants (0,5%), indicating that the genetic testing for the p.R337H mutation could potentially be included in existing screening panels. Similarly, Giacomazzi et al. (2014) investigated the prevalence of the p.R337H mutation in two different Brazilian groups of women diagnosed with breast cancer: one composed by affected individuals with a family history compatible with hereditary breast cancer but no LFS/LFL features and another one, by women unselected for family history The authors found mutation frequencies of 3,4% and 8,6% for each group, respectively. Due to this frequency, they proposed that this mutation may play an important role in the incidence of breast cancer in Brazil.

These findings, along with ours, strengthen the importance of suggesting concomitant TP53 p.R337H genetic testing for women affected by breast cancer before age 45, irrespective of family history, particularly in the South and Southeast of Brazil, where the prevalence of a germline TP53 is considerably higher than elsewhere in the world. The inclusion of this group of patients would potentially avoid LFS/LFL underdiagnosis and inappropriate genetic counseling.

Acknowledgments

The authors wish to thank the participation of all the families included in this research, the Department of Oncogenetics for selection of candidate families and the A.C. Camargo Cancer Center BioBank staff for technical support. Financial support was provided by the National Institute of Science and Technology in Oncogenomics (INCITO – process 2008/57887-9).

Footnotes

Associate Editor: Pierre Hainaut

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