Ethnicity-specific BRCA1, BRCA2, PALB2, and ATM pathogenic alleles in breast and ovarian cancer patients from the North Caucasus
Background Mountain areas of the North Caucasus host several large ethnic communities that have preserved their national identity over the centuries. Methods This study involved high-grade serous ovarian cancer (HGSOC) and breast cancer (BC) patients from Dagestan (HGSOC: 37; BC: 198), Kabardino-Bal...
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Published in: | Breast cancer research and treatment Vol. 203; no. 2; pp. 307 - 315 |
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Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
New York
Springer US
2024
Springer Nature B.V |
Subjects: | |
Online Access: | Get full text |
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Summary: | Background
Mountain areas of the North Caucasus host several large ethnic communities that have preserved their national identity over the centuries.
Methods
This study involved high-grade serous ovarian cancer (HGSOC) and breast cancer (BC) patients from Dagestan (HGSOC: 37; BC: 198), Kabardino-Balkaria (HGSOC: 68; BC: 155), North Ossetia (HGSOC: 51; BC: 104), Chechnya (HGSOC: 68; BC: 79), Ingushetia (HGSOC: 19; BC: 103), Karachay-Cherkessia (HGSOC: 13; BC: 47), and several Armenian settlements (HGSOC: 16; BC: 101). The group of BC patients was enriched by young-onset and/or family history-positive and/or bilateral and/or receptor triple-negative cases. The entire coding region of
BRCA1, BRCA2, PALB2,
and
ATM
genes was analyzed by next-generation sequencing.
Results
A significant contribution of
BRCA1/2
pathogenic variants (PVs) to HGSOC and BC development was observed across all North Caucasus regions (HGSOC: 19–39%; BC: 6–13%). Founder alleles were identified in all ethnic groups studied, e.g.,
BRCA1
c.3629_3630delAG in Chechens,
BRCA2
c.6341delC in North Ossetians,
BRCA2
c.5351dupA in Ingush, and
BRCA1
c.2907_2910delTAAA in Karachays. Some
BRCA1/2
alleles, particularly
BRCA2
c.9895C > T, were shared by several nationalities.
ATM
PVs were detected in 14 patients, with c.1673delG and c.8876_8879delACTG alleles occurring twice each.
PALB2
heterozygosity was observed in 5 subjects, with one variant seen in 2 unrelated women.
Conclusion
This study adds to the evidence for the global-wide contribution of
BRCA1
/
2
genes to HGSOC and BC morbidity, although the spectrum of their PVs is a subject of ethnicity-specific variations. The data on founder
BRCA1/2
alleles may be considered when adjusting the
BRCA1/2
testing procedure to the ethnic origin of patients. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0167-6806 1573-7217 |
DOI: | 10.1007/s10549-023-07135-3 |