Aberrations of the number of copies (CNA) in the genome of luminal B breast tumor

Aim. To describe the CNA (Copy Number Aberration) landscape of luminal B breast tumor before treatment.Materials and methods. The study included 100 patients with breast cancer (BC) of luminal B subtype for which a biopsy of the tumor material was performed prior to neoadjuvant chemotherapy (NAC). T...

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Main Authors: M. K. Ibragimova, M. M. Tsyganov, E. M. Slonimskaya, N. V. Litviakov
Format: Article
Language:English
Published: Siberian State Medical University (Tomsk) 2020-10-01
Series:Бюллетень сибирской медицины
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Online Access:https://bulletin.ssmu.ru/jour/article/view/2973
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author M. K. Ibragimova
M. M. Tsyganov
E. M. Slonimskaya
N. V. Litviakov
author_facet M. K. Ibragimova
M. M. Tsyganov
E. M. Slonimskaya
N. V. Litviakov
author_sort M. K. Ibragimova
collection DOAJ
description Aim. To describe the CNA (Copy Number Aberration) landscape of luminal B breast tumor before treatment.Materials and methods. The study included 100 patients with breast cancer (BC) of luminal B subtype for which a biopsy of the tumor material was performed prior to neoadjuvant chemotherapy (NAC). The tumor DNA was examined using a CytoScan HD Array microarray (Affymetrix, USA). The obtained microarray data were correlated with NAC efficacy.Results. The study showed that loci 1q32.1-32.3, 1q41-42.2, and 8q24.21 had the highest frequency of  amplifications (in more than 65% of patients). The highest deletion frequency (in more than 60% of patients) was found in loci 16q21, 16q22.1, 16q23.1-24.1, 17p13.1, and 17p12. Trisomy was most often observed in chromosomes 7, 8, 12, and 17, and monosomy in chromosomes 3, 4, 9, 11, 18, and X-chromosomes. The CNA landscape of luminal B subtype breast tumors is different from triple-negative breast cancer. The largest difference in the frequency of amplifications between patients with an objective response to NAC and patients with no response to NAC was shown in 1q24.2-42.2 loci (46%), and the largest difference in the frequency of deletions (more than 30%) between groups was in regions 6q16. 3, 11p15.4, 11q23.1, and 16q22.2-22.3. These loci can be considered potential predictive markers.Conclusion. The research determined loci with the highest amplification and deletion frequencies for luminal B breast cancer. Potential predictive markers for the given molecular subtype were identified.
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spelling doaj-art-e4d62c4a4f3c423582104e0ae8a1217d2025-08-20T03:38:06ZengSiberian State Medical University (Tomsk)Бюллетень сибирской медицины1682-03631819-36842020-10-01193222810.20538/1682-0363-2020-3-22-281641Aberrations of the number of copies (CNA) in the genome of luminal B breast tumorM. K. Ibragimova0M. M. Tsyganov1E. M. Slonimskaya2N. V. Litviakov3Саnсеr Rеsеаrсh Institute, Tomsk National Research Medical Center of Russian Academy of SciencesСаnсеr Rеsеаrсh Institute, Tomsk National Research Medical Center of Russian Academy of SciencesSaint-Petersburg State UniversityСаnсеr Rеsеаrсh Institute, Tomsk National Research Medical Center of Russian Academy of SciencesAim. To describe the CNA (Copy Number Aberration) landscape of luminal B breast tumor before treatment.Materials and methods. The study included 100 patients with breast cancer (BC) of luminal B subtype for which a biopsy of the tumor material was performed prior to neoadjuvant chemotherapy (NAC). The tumor DNA was examined using a CytoScan HD Array microarray (Affymetrix, USA). The obtained microarray data were correlated with NAC efficacy.Results. The study showed that loci 1q32.1-32.3, 1q41-42.2, and 8q24.21 had the highest frequency of  amplifications (in more than 65% of patients). The highest deletion frequency (in more than 60% of patients) was found in loci 16q21, 16q22.1, 16q23.1-24.1, 17p13.1, and 17p12. Trisomy was most often observed in chromosomes 7, 8, 12, and 17, and monosomy in chromosomes 3, 4, 9, 11, 18, and X-chromosomes. The CNA landscape of luminal B subtype breast tumors is different from triple-negative breast cancer. The largest difference in the frequency of amplifications between patients with an objective response to NAC and patients with no response to NAC was shown in 1q24.2-42.2 loci (46%), and the largest difference in the frequency of deletions (more than 30%) between groups was in regions 6q16. 3, 11p15.4, 11q23.1, and 16q22.2-22.3. These loci can be considered potential predictive markers.Conclusion. The research determined loci with the highest amplification and deletion frequencies for luminal B breast cancer. Potential predictive markers for the given molecular subtype were identified.https://bulletin.ssmu.ru/jour/article/view/2973breast cancermicroarray analysisdeletionsamplificationsneoadjuvant chemotherapy
spellingShingle M. K. Ibragimova
M. M. Tsyganov
E. M. Slonimskaya
N. V. Litviakov
Aberrations of the number of copies (CNA) in the genome of luminal B breast tumor
Бюллетень сибирской медицины
breast cancer
microarray analysis
deletions
amplifications
neoadjuvant chemotherapy
title Aberrations of the number of copies (CNA) in the genome of luminal B breast tumor
title_full Aberrations of the number of copies (CNA) in the genome of luminal B breast tumor
title_fullStr Aberrations of the number of copies (CNA) in the genome of luminal B breast tumor
title_full_unstemmed Aberrations of the number of copies (CNA) in the genome of luminal B breast tumor
title_short Aberrations of the number of copies (CNA) in the genome of luminal B breast tumor
title_sort aberrations of the number of copies cna in the genome of luminal b breast tumor
topic breast cancer
microarray analysis
deletions
amplifications
neoadjuvant chemotherapy
url https://bulletin.ssmu.ru/jour/article/view/2973
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AT nvlitviakov aberrationsofthenumberofcopiescnainthegenomeofluminalbbreasttumor