Identification of a possible somatic BRCA1 mutation affecting translation efficiency in an early-onset sporadic breast cancer patient.

Mutations in the BRCA1 gene account for up to 80% of cases of familial breast cancers (1). However, the majority of breast cancers are sporadic and only 10% of cases show a familial basis. No alterations of the BRCA1 gene have been associated with sporadic breast cancer cases, although other cancers, like sporadic ovarian cancers, display somatic inactivation of BRCA1 (2). However, decreased BRCA1 gene expression is frequently found in sporadic breast cancer in the absence of direct mutations in the coding region (3). It is plausible that BRCA1 down-modulation occurs by epigenetic mechanisms involving altered upstream regulatory regions, such as hypermethylation of the promoter region (4), or other factors implicated in the complex regulatory mechanism. We report here the description of a novel BRCA1 gene mutation potentially affecting BRCA1 gene expression in a woman with sporadic breast cancer who was a case subject in a population-based retrospective screening for BRCA1 gene involvement in 96 sporadic breast cancer cases. The women, 32 years of age, was diagnosed with a grade III infiltrating ductal carcinoma of the breast and treated with mastectomy, ancillary lymph node resection, radiotherapy, and six cycles of standard adjuvant chemotherapy. The patient was then cancer free for 10 months. However, the tumor recurred and the patient, who was treated with palliative chemotherapy, died 2 years later. This woman’s genomic DNA was available from the primary tumor and one metastatic lymph node. Full-length RNA single-strand conformation polymorphism analysis of each of the 24 BRCA1 gene exons revealed several common sequence polymorphisms and a unique aberrant banding pattern within exon 2 in both tumor samples. The exon 2 sequences were amplified by use of the polymerase chain reaction and the product subjected to direct sequencing. DNA sequence information was obtained from both tumor samples and the sequence was confirmed on both strands. A single base transversion (G to C) was identified at nucleotide position 117, three nucleotides 58 of the ATG initiation codon, within a ‘‘Kozak’’ consensus motif (5) for the start of translation (Fig. 1, A). Direct sequencing of the BRCA1 gene confirmed by multiple sequence reactions from independent polymerase chain reaction reactions (both manual and automated analysis using a Vistra DNA Sequencer 725, Amersham, Little Chalfont, Buckinghamshire, U.K.) showed two bands, a more intense band corresponded to the mutated C and a fainter band corresponding to the normal G. The presence of both bands are consistent with the fact that each tumor sample was composed of a mixture of malignant cells and of nonmalignant stromal cells. No messenger RNA translation studies were performed based on this information. However, it is known that a purine to pyrimidine base change located three nucleotides 58 of Kozak consensus sequence motif severely affects translation efficiency (Fig. 1, B) (6). These data are consistent with the observation that 97% of all vertebrate messenger RNAs carry a purine at this ‘‘-3’’ position of the translation start motif (7). It is also noteworthy that the sequence context is well conserved for the major translation initiation site of the BRCA1 gene among human, mouse, and rat gene homologues (GenBank accession numbers: U14680, U32446, and AF036760, respectively). Because of the early onset of the tumor, we investigated the possibility that