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Affected individuals from 431 families gave blood for mutational analysis in BRCA1 and BRCA2 mainly to develop genetic tests for their family. Individuals were eligible if there was at least a 50% chance of a gene predisposing to breast cancer (not necessarily BRCA1/2) in their family. Assessment was made using the Cancer and Steroid Hormone (CASH) dataset and the Claus curves.1,2 A minimal requirement was two close relatives with breast cancer before the age of 50 years, but combinations of male and female breast cancer, and breast and ovarian cancer were particularly identified. An exception to this were two research projects where population based cases of breast cancer before the age of 31 years3 and sporadic breast cancer before the age of 36 years4 were screened for both genes. Male breast cancer (MBC) families presenting to the clinic with at least one MBC before the age of 60 years or at any age if female breast cancer had occurred were screened for BRCA2.5
Initial screening for mutations involved a whole gene assessment using single strand conformational polymorphism (SSCP) analysis and protein truncation testing (PTT) of exon 11 in each gene. All mutations were confirmed, in both orientations, by direct fluorescent sequencing of the appropriate exon. We excluded one exon 13 duplication and two exonic deletions detected on screening 95 BRCA1 negative breast/ovarian families. A further two exon 13 duplications in five subsequent BRCA1 negative breast/ovary families originating from east of the Pennines were also excluded. Of the non large-scale rearrangement mutations, 26/78 (33%) were detected outside the commonly screened regions of BRCA1 (exons 2, 11, 20) in the UK (table 1). Similarly 15/50 (30%) BRCA2 mutations were detected outside exons 10 and 11.
In an attempt to assess the sensitivity of our techniques, we studied the outcome of testing in families with two or more confirmed ovarian cancers, which also had a total of at least four breast/ovarian cancers (breast cancer before the age of 60 years) and male breast cancer families with a similar four or more breast/ovarian cancers in total. Of breast/ovarian families fulfilling the above criteria, 25/38 (66%) had pathogenic BRCA1 mutations (five had BRCA2 mutations and one had a BRCA1 deletion) and 9/14 (64%) male breast cancer families had pathogenic BRCA2 mutations.5 These results would suggest high sensitivity for the techniques, particularly for BRCA2. From Breast Cancer Linkage Consortium data, 90% of such breast-ovarian families were linked to BRCA1, and 76% of male breast cancer families were linked to BRCA2.6 This would suggest sensitivity of close to 85% for BRCA2 and 73% for BRCA1. However, previous attempts to validate SSCP have shown that only 65–72% of BRCA1 mutations are correctly ascribed by SSCP.7,8 PTT detected all 15 deleterious mutations in one study, but SSCP only detected 10.8 Nevertheless sensitivity is not just dependent on the proportion of different mutations detected, but on the frequency of each in a particular population. Taking all these factors into account we have estimated that our whole gene testing technique (without testing for large deletions or duplications) would have a sensitivity of at least 66% (see table 2), and that about 6% (4/66) of our breast/ovarian families have deletions or large-scale rearrangements.
Partial or targeted mutation screening of BRCA1/2 in non-founder populations of limited value.
Whole gene screening adding a deletion strategy such as multiplex ligation dependent probe amplification will give good negative predictive value particularly in breast only families where risks of ovarian cancer can be substantially downgraded.
The 546→T mutation in exon 7 BRCA1 is missed by most non-sequencing techniques and appears to be a common UK mutation, which has spread to North America.
Samples from affected family members from 431 non-Jewish families with a history of breast/ovarian cancer, which had been obtained from a consultee in northwest England, were screened for the presence of BRCA1 mutations. We also screened 284 such families for BRCA2 mutations.
In total, 466 families were tested for mutations in one or other gene and 318 for both genes. Both BRCA1 and BRCA2 were screened by whole gene screening techniques; 83 (19%) and 50 (18%) pathogenic mutations were identified in BRCA1 and BRCA2, respectively.
The proportion of breast/ovarian cancers attributable to BRCA1 or BRCA2 depends on the ethnic origin of families. Many countries or ethnic groups have particular founder mutations that are not seen in other populations. In countries with a small founder population, very few mutations may account for the vast majority of breast cancer families. The Ashkenazi Jewish population have three founder mutations, 185delAG and 5382insC in BRCA1, and 6174delT in BRCA2, which are found in over 2% of the this population. At least two studies have shown that one of the three mutations is present in the majority (59%–80%) of high risk families9,10 , and all three account for nearly all of the involvement of these genes in families. Another country with a small number of mutations is Iceland, where one mutation, BRCA2 995del5, accounts for most familial breast cancer.11 Populations that are more outbred, such as the UK, have larger numbers of mutations, and founder mutations occur at lower frequencies. Even the exon 13 duplication, a known UK founder12 , is relatively rare outside Yorkshire and Trent (east of the Pennines) as demonstrated by our low frequency of 1/95 (1%) in BRCA1 negative breast/ovary families. Nevertheless, many laboratories in the UK have tried to develop a targeted approach to screening, concentrating on the large exons (exon 11 in both genes and 10 in BRCA2) and the smaller exons commonly reported to be involved, such as 2 and 20 in BRCA1. This cuts down the number of PCR assays using PTT to as few as five for BRCA1 and four for BRCA2. However, failure to use another technique such as SSCP at the beginning and end of the large exons would potentially miss our two most common mutations, 2157 delG in BRCA2 (nine families) and 4184 del TTAC in BRCA1 (12 families). These mutations are not reliably detected by PTT as they are at the extreme ends of exon 11 in both genes.13 This would therefore add four PCR assays to BRCA2 testing and two to BRCA1. Even with these additional assays, sensitivity for the whole gene is boosted from only around 33% to 44–46% (table 2). The utility of a negative test in this situation is negligible. However, once sensitivity rises beyond 66% the chances of a BRCA1/2 mutation being present in the family at least halves using Bayes’ theorum. Thus in a family with 4–5 breast cancers before the age of 60 years (no ovarian or male breast cancer), which has around a 33% chance of being due to BRCA1/2,6 a negative test would substantially reduce the estimate of ovarian cancer risk for family members. Taking an average risk for BRCA1/2 of 30% lifetime chance for ovarian cancer, the risk estimate for an affected woman with breast cancer could be as much as an extra 10% prior to testing. However, with a negative whole gene screen this extra ovarian cancer risk will fall to below 5%, and 2.5% for at-risk unaffected relatives.
Adding an exon deletion/duplication strategy such as multiplex ligation dependent probe amplification (MLPA)14 would add an extra 6% sensitivity in our sample (table 1), but in other populations such as the Netherlands could account for up to 27% or more of BRCA1 pathogenic mutations.15 As this is a single assay, it or a similar test should probably now be added to all BRCA screening strategies. As can be seen from table 2 even direct sequencing plus a technique such as MLPA does not reach 100% sensitivity. This is because mutations buried in the intron that affect splicing, or effects outside the gene that affect RNA transcription would not be detected. Indeed, chromosome translocations not affecting an exon would also be undetected. Nevertheless many pathogenic mutations might be inappropriately labelled “undetected”, as many missense changes of uncertain pathogenic significance remain unclassified. Improvements in classifying these variants should boost mutation detection sensitivity further.16
Our results would also suggest that for the UK at least exon 11 in BRCA1 does not account for more mutations than would be predicted from its size alone. Only 48/83 (58%) pathogenic BRCA1 mutations were detected in exon 11, which is equivalent to its contribution of 60% to the coding sequence. Similarly only 5/34 (14%) of the non-Jewish non-exon 11 BRCA1 mutations were in exons 2 and 20. Indeed exons 5 and 7 contribute more mutations individually than either exons 2 or 20. The finding of six exon 7 546 G→T mutations is of particular significance. We were initially unable to cover the whole of this exon by SSCP due to the large number of repeat sequences in the intron. It is our understanding from other groups that virtually no laboratory has been able to obtain workable non-sequencing results for exon 7. Eventually we sequenced exon 7 in 30 breast/ovarian families previously negative on BRCA1 testing. Three families tested positive for the 546 G→T mutation. We have now tested 201/354 families testing negative for other BRCA1 pathogenic changes and identified six of these mutations. Although the most likely families have been tested it is possible that at least a further two mutations would be identified on testing the remainder. It is likely this mutation is more than just a local founder mutation as it has been recorded 30 times on the BIC website17 by Myriad Genetics and only twice by other laboratories. Given the frequency of this mutation in our northwest population and Myriad it would suggest that many laboratories are missing the mutation even if they are screening exon 7 unless they are using sequencing techniques. It would also suggest that this mutation should be incorporated into even a partial gene screen in the UK.
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