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Prevalence of BRCA1 and BRCA2 gene mutations in Chinese patients with high‐risk breast cancer

BACKGROUND: Breast cancer is the most common cancer among women worldwide. Here, we report the prevalence of BRCA1/2 mutations in patients with high‐risk breast cancer from Inner Mongolia and Jilin, China, which was a part of a nationwide project on the detection of BRCA1/2 mutations in Chinese pati...

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Autores principales: Wang, Xiaozhen, Liu, Haimeng, Maimaitiaili, Amina, Zhao, Gang, Li, Sijie, Lv, Zheng, Wu, Di, Shi, Aiping, Guan, Xin, Jia, Hongyao, Li, Menghan, Song, Dong, Kang, Lihua, Han, Bing, Fu, Tong, Yang, Ming, Zhu, Zhu, Du, Ye, Song, Yanqiu, Hong, Jinghui, Fan, Zhimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565549/
https://www.ncbi.nlm.nih.gov/pubmed/30968603
http://dx.doi.org/10.1002/mgg3.677
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author Wang, Xiaozhen
Liu, Haimeng
Maimaitiaili, Amina
Zhao, Gang
Li, Sijie
Lv, Zheng
Wu, Di
Shi, Aiping
Guan, Xin
Jia, Hongyao
Li, Menghan
Song, Dong
Kang, Lihua
Han, Bing
Fu, Tong
Yang, Ming
Zhu, Zhu
Du, Ye
Song, Yanqiu
Hong, Jinghui
Fan, Zhimin
author_facet Wang, Xiaozhen
Liu, Haimeng
Maimaitiaili, Amina
Zhao, Gang
Li, Sijie
Lv, Zheng
Wu, Di
Shi, Aiping
Guan, Xin
Jia, Hongyao
Li, Menghan
Song, Dong
Kang, Lihua
Han, Bing
Fu, Tong
Yang, Ming
Zhu, Zhu
Du, Ye
Song, Yanqiu
Hong, Jinghui
Fan, Zhimin
author_sort Wang, Xiaozhen
collection PubMed
description BACKGROUND: Breast cancer is the most common cancer among women worldwide. Here, we report the prevalence of BRCA1/2 mutations in patients with high‐risk breast cancer from Inner Mongolia and Jilin, China, which was a part of a nationwide project on the detection of BRCA1/2 mutations in Chinese patients with hereditary breast cancer. METHODS: According to the criteria, index patients from a total of 245 independent families were initially recruited. All 49 exons of BRCA1 and BRCA2 and adjacent noncoding regions were screened for mutations based on next‐generation sequencing from collected saliva. RESULTS: We detected 17 BRCA1/2 variants in 18 of 216 (8.3%) index patients with high‐risk breast cancer. Among these, seven mutations were novel, including four BRCA1 mutations (c.123_124delCAinsAT, c.5093_5096delCTAA, c.5396‐2A>G, and c.2054delinsGAAGAGTAACAAGTAAGAAGAGTAACAAGAAG), and three BRCA2 mutations (c.304A>T, c.7552_7553insT, and c.9548_9549insA). The BRCA1/2 variants were identified in 14% (8/57) of the patients with triple‐negative breast cancer and in 6.3% (10/159) of the patients with non‐triple‐negative breast cancer. There was no significant difference between the two groups (p = 0.07). A higher frequency for BRCA1 mutations was observed in patients with triple‐negative breast cancer than in those with non‐triple‐negative breast cancer (12.3% vs. 2.5%, p = 0.004). The frequencies of the BRCA2 mutations were not significantly different between patients with triple‐negative breast cancer and those with non‐triple‐negative breast cancer (1.8% vs. 3.8%, p = 0.46). CONCLUSION: We found that patients with triple‐negative breast cancer had a higher frequency of BRCA1 mutations than those with non‐triple‐negative breast cancer. In this study, no significant associations between the BRCA1/2 mutation status and age, family history of breast cancer, ovarian cancer, pancreatic cancer and prostate cancer, number of primary lesions, tumor size, or lymph node metastasis were observed.
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spelling pubmed-65655492019-06-20 Prevalence of BRCA1 and BRCA2 gene mutations in Chinese patients with high‐risk breast cancer Wang, Xiaozhen Liu, Haimeng Maimaitiaili, Amina Zhao, Gang Li, Sijie Lv, Zheng Wu, Di Shi, Aiping Guan, Xin Jia, Hongyao Li, Menghan Song, Dong Kang, Lihua Han, Bing Fu, Tong Yang, Ming Zhu, Zhu Du, Ye Song, Yanqiu Hong, Jinghui Fan, Zhimin Mol Genet Genomic Med Original Articles BACKGROUND: Breast cancer is the most common cancer among women worldwide. Here, we report the prevalence of BRCA1/2 mutations in patients with high‐risk breast cancer from Inner Mongolia and Jilin, China, which was a part of a nationwide project on the detection of BRCA1/2 mutations in Chinese patients with hereditary breast cancer. METHODS: According to the criteria, index patients from a total of 245 independent families were initially recruited. All 49 exons of BRCA1 and BRCA2 and adjacent noncoding regions were screened for mutations based on next‐generation sequencing from collected saliva. RESULTS: We detected 17 BRCA1/2 variants in 18 of 216 (8.3%) index patients with high‐risk breast cancer. Among these, seven mutations were novel, including four BRCA1 mutations (c.123_124delCAinsAT, c.5093_5096delCTAA, c.5396‐2A>G, and c.2054delinsGAAGAGTAACAAGTAAGAAGAGTAACAAGAAG), and three BRCA2 mutations (c.304A>T, c.7552_7553insT, and c.9548_9549insA). The BRCA1/2 variants were identified in 14% (8/57) of the patients with triple‐negative breast cancer and in 6.3% (10/159) of the patients with non‐triple‐negative breast cancer. There was no significant difference between the two groups (p = 0.07). A higher frequency for BRCA1 mutations was observed in patients with triple‐negative breast cancer than in those with non‐triple‐negative breast cancer (12.3% vs. 2.5%, p = 0.004). The frequencies of the BRCA2 mutations were not significantly different between patients with triple‐negative breast cancer and those with non‐triple‐negative breast cancer (1.8% vs. 3.8%, p = 0.46). CONCLUSION: We found that patients with triple‐negative breast cancer had a higher frequency of BRCA1 mutations than those with non‐triple‐negative breast cancer. In this study, no significant associations between the BRCA1/2 mutation status and age, family history of breast cancer, ovarian cancer, pancreatic cancer and prostate cancer, number of primary lesions, tumor size, or lymph node metastasis were observed. John Wiley and Sons Inc. 2019-04-09 /pmc/articles/PMC6565549/ /pubmed/30968603 http://dx.doi.org/10.1002/mgg3.677 Text en © 2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Wang, Xiaozhen
Liu, Haimeng
Maimaitiaili, Amina
Zhao, Gang
Li, Sijie
Lv, Zheng
Wu, Di
Shi, Aiping
Guan, Xin
Jia, Hongyao
Li, Menghan
Song, Dong
Kang, Lihua
Han, Bing
Fu, Tong
Yang, Ming
Zhu, Zhu
Du, Ye
Song, Yanqiu
Hong, Jinghui
Fan, Zhimin
Prevalence of BRCA1 and BRCA2 gene mutations in Chinese patients with high‐risk breast cancer
title Prevalence of BRCA1 and BRCA2 gene mutations in Chinese patients with high‐risk breast cancer
title_full Prevalence of BRCA1 and BRCA2 gene mutations in Chinese patients with high‐risk breast cancer
title_fullStr Prevalence of BRCA1 and BRCA2 gene mutations in Chinese patients with high‐risk breast cancer
title_full_unstemmed Prevalence of BRCA1 and BRCA2 gene mutations in Chinese patients with high‐risk breast cancer
title_short Prevalence of BRCA1 and BRCA2 gene mutations in Chinese patients with high‐risk breast cancer
title_sort prevalence of brca1 and brca2 gene mutations in chinese patients with high‐risk breast cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6565549/
https://www.ncbi.nlm.nih.gov/pubmed/30968603
http://dx.doi.org/10.1002/mgg3.677
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