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The Ethnic-Specific Spectrum of Germline Nucleotide Variants in DNA Damage Response and Repair Genes in Hereditary Breast and Ovarian Cancer Patients of Tatar Descent

The Russian population consists of more than 100 ethnic groups, presenting a unique opportunity for the identification of hereditary pathogenic mutations. To gain insight into the landscape of heredity pathogenic variants, we employed targeted next-generation sequencing to analyze the germline mutat...

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Autores principales: Brovkina, Olga I., Shigapova, Leila, Chudakova, Daria A., Gordiev, Marat G., Enikeev, Rafael F., Druzhkov, Maxim O., Khodyrev, Dmitriy S., Shagimardanova, Elena I., Nikitin, Alexey G., Gusev, Oleg A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176317/
https://www.ncbi.nlm.nih.gov/pubmed/30333958
http://dx.doi.org/10.3389/fonc.2018.00421
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author Brovkina, Olga I.
Shigapova, Leila
Chudakova, Daria A.
Gordiev, Marat G.
Enikeev, Rafael F.
Druzhkov, Maxim O.
Khodyrev, Dmitriy S.
Shagimardanova, Elena I.
Nikitin, Alexey G.
Gusev, Oleg A.
author_facet Brovkina, Olga I.
Shigapova, Leila
Chudakova, Daria A.
Gordiev, Marat G.
Enikeev, Rafael F.
Druzhkov, Maxim O.
Khodyrev, Dmitriy S.
Shagimardanova, Elena I.
Nikitin, Alexey G.
Gusev, Oleg A.
author_sort Brovkina, Olga I.
collection PubMed
description The Russian population consists of more than 100 ethnic groups, presenting a unique opportunity for the identification of hereditary pathogenic mutations. To gain insight into the landscape of heredity pathogenic variants, we employed targeted next-generation sequencing to analyze the germline mutation load in the DNA damage response and repair genes of hereditary breast and ovary cancer syndrome (HBOCS) patients of Tatar ethnicity, which represents ~4% of the total Russian population. Several pathogenic mutations were identified in DNA double-strand break repair genes, and the spectrum of these markers in Tatar patients varied from that previously reported for patients of Slavic ancestry. The CDK12 gene encodes cyclin-dependent kinase 12, the key transcriptional regulator of the genes involved in DNA damage response and repair. CDK12 analysis in a cohort of HBOCS patients of Tatar decent identified a c.1047-2A>G nucleotide variant in the CDK12 gene in 8 of the 106 cases (7.6%). The c.1047-2A>G nucleotide variant was identified in 1 of the 93 (1.1%) HBOCS patients with mixed or unknown ethnicity and in 1 of the 238 (0.42%) healthy control patients of mixed ethnicity (Tatars and non-Tatars) (p = 0.0066, OR = 11.18, CI 95% = 1.53–492.95, Tatar and non-Tatar patients vs. healthy controls). In a group of mixed ethnicity patients from Tatarstan, with sporadic breast and/or ovarian cancer, this nucleotide variant was detected in 2 out of 93 (2.2%) cases. In a cohort of participants of Slavic descent from Moscow, comprising of 95 HBOCS patients, 80 patients with sporadic breast and/or ovarian cancer, and 372 healthy controls, this nucleotide variant was absent. Our study demonstrates a strong predisposition for the CDK12 c.1047-2A>G nucleotide variant in HBOCS in patients of Tatar ethnicity and identifies CDK12 as a novel gene involved in HBOCS susceptibility.
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spelling pubmed-61763172018-10-17 The Ethnic-Specific Spectrum of Germline Nucleotide Variants in DNA Damage Response and Repair Genes in Hereditary Breast and Ovarian Cancer Patients of Tatar Descent Brovkina, Olga I. Shigapova, Leila Chudakova, Daria A. Gordiev, Marat G. Enikeev, Rafael F. Druzhkov, Maxim O. Khodyrev, Dmitriy S. Shagimardanova, Elena I. Nikitin, Alexey G. Gusev, Oleg A. Front Oncol Oncology The Russian population consists of more than 100 ethnic groups, presenting a unique opportunity for the identification of hereditary pathogenic mutations. To gain insight into the landscape of heredity pathogenic variants, we employed targeted next-generation sequencing to analyze the germline mutation load in the DNA damage response and repair genes of hereditary breast and ovary cancer syndrome (HBOCS) patients of Tatar ethnicity, which represents ~4% of the total Russian population. Several pathogenic mutations were identified in DNA double-strand break repair genes, and the spectrum of these markers in Tatar patients varied from that previously reported for patients of Slavic ancestry. The CDK12 gene encodes cyclin-dependent kinase 12, the key transcriptional regulator of the genes involved in DNA damage response and repair. CDK12 analysis in a cohort of HBOCS patients of Tatar decent identified a c.1047-2A>G nucleotide variant in the CDK12 gene in 8 of the 106 cases (7.6%). The c.1047-2A>G nucleotide variant was identified in 1 of the 93 (1.1%) HBOCS patients with mixed or unknown ethnicity and in 1 of the 238 (0.42%) healthy control patients of mixed ethnicity (Tatars and non-Tatars) (p = 0.0066, OR = 11.18, CI 95% = 1.53–492.95, Tatar and non-Tatar patients vs. healthy controls). In a group of mixed ethnicity patients from Tatarstan, with sporadic breast and/or ovarian cancer, this nucleotide variant was detected in 2 out of 93 (2.2%) cases. In a cohort of participants of Slavic descent from Moscow, comprising of 95 HBOCS patients, 80 patients with sporadic breast and/or ovarian cancer, and 372 healthy controls, this nucleotide variant was absent. Our study demonstrates a strong predisposition for the CDK12 c.1047-2A>G nucleotide variant in HBOCS in patients of Tatar ethnicity and identifies CDK12 as a novel gene involved in HBOCS susceptibility. Frontiers Media S.A. 2018-10-02 /pmc/articles/PMC6176317/ /pubmed/30333958 http://dx.doi.org/10.3389/fonc.2018.00421 Text en Copyright © 2018 Brovkina, Shigapova, Chudakova, Gordiev, Enikeev, Druzhkov, Khodyrev, Shagimardanova, Nikitin and Gusev. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Brovkina, Olga I.
Shigapova, Leila
Chudakova, Daria A.
Gordiev, Marat G.
Enikeev, Rafael F.
Druzhkov, Maxim O.
Khodyrev, Dmitriy S.
Shagimardanova, Elena I.
Nikitin, Alexey G.
Gusev, Oleg A.
The Ethnic-Specific Spectrum of Germline Nucleotide Variants in DNA Damage Response and Repair Genes in Hereditary Breast and Ovarian Cancer Patients of Tatar Descent
title The Ethnic-Specific Spectrum of Germline Nucleotide Variants in DNA Damage Response and Repair Genes in Hereditary Breast and Ovarian Cancer Patients of Tatar Descent
title_full The Ethnic-Specific Spectrum of Germline Nucleotide Variants in DNA Damage Response and Repair Genes in Hereditary Breast and Ovarian Cancer Patients of Tatar Descent
title_fullStr The Ethnic-Specific Spectrum of Germline Nucleotide Variants in DNA Damage Response and Repair Genes in Hereditary Breast and Ovarian Cancer Patients of Tatar Descent
title_full_unstemmed The Ethnic-Specific Spectrum of Germline Nucleotide Variants in DNA Damage Response and Repair Genes in Hereditary Breast and Ovarian Cancer Patients of Tatar Descent
title_short The Ethnic-Specific Spectrum of Germline Nucleotide Variants in DNA Damage Response and Repair Genes in Hereditary Breast and Ovarian Cancer Patients of Tatar Descent
title_sort ethnic-specific spectrum of germline nucleotide variants in dna damage response and repair genes in hereditary breast and ovarian cancer patients of tatar descent
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176317/
https://www.ncbi.nlm.nih.gov/pubmed/30333958
http://dx.doi.org/10.3389/fonc.2018.00421
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