Abstract
BackgroundThe incidence of breast cancer among young women (aged ≤40 years) has increased in North America and Europe. Fewer than 10% of cases among young women are attributable to inherited BRCA1 or BRCA2 mutations, suggesting an important role for somatic mutations. This study investigated genomic differences between young- and older-onset breast tumours.MethodsIn this study we characterized the mutational landscape of 89 young-onset breast tumours (≤40 years) and examined differences with 949 older-onset tumours (> 40 years) using data from The Cancer Genome Atlas. We examined mutated genes, mutational load, and types of mutations. We used complementary R packages “deconstructSigs” and “SomaticSignatures” to extract mutational signatures. A recursively partitioned mixture model was used to identify whether combinations of mutational signatures were related to age of onset.ResultsOlder patients had a higher proportion of mutations in PIK3CA, CDH1, and MAP3K1 genes, while young-onset patients had a higher proportion of mutations in GATA3 and CTNNB1. Mutational load was lower for young-onset tumours, and a higher proportion of these mutations were C > A mutations, but a lower proportion were C > T mutations compared to older-onset tumours. The most common mutational signatures identified in both age groups were signatures 1 and 3 from the COSMIC database. Signatures resembling COSMIC signatures 2 and 13 were observed among both age groups. We identified a class of tumours with a unique combination of signatures that may be associated with young age of onset.ConclusionsThe results of this exploratory study provide some evidence that the mutational landscape and mutational signatures among young-onset breast cancer are different from those of older-onset patients. The characterization of young-onset tumours could provide clues to their etiology which may inform future prevention. Further studies are required to confirm our findings.
Highlights
The incidence of breast cancer among young women has increased in North America and Europe
We reduced the risk for false discovery by limiting the number of genes we investigated to this set of genes which are likely relevant to breast cancer
Given that Single nucleotide variant (SNV) comprise a large proportion of somatic mutations, we reported the SNV-only mutational load, and tested difference by age groups
Summary
The incidence of breast cancer among young women (aged ≤40 years) has increased in North America and Europe. Its estimated global incidence was 1.68 million in 2012, accounting for 25% of cancer diagnoses among women of all ages [1]. Among women under the age of 40 in the United States, breast cancer accounts for over 40% of cancer diagnoses [2]. Epidemiological studies demonstrated a trend of rising incidence among Canadian women between 1969 and 2012, and among women in the United States from 2004 to 2015 [5, 6]. A European study showed an average increase of 3 and 1% annually among women aged 20–29, and 30–39, respectively [3]
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