Cargando…
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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783426667562139648 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6565549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT wangxiaozhen prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT liuhaimeng prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT maimaitiailiamina prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT zhaogang prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT lisijie prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT lvzheng prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT wudi prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT shiaiping prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT guanxin prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT jiahongyao prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT limenghan prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT songdong prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT kanglihua prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT hanbing prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT futong prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT yangming prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT zhuzhu prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT duye prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT songyanqiu prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT hongjinghui prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer AT fanzhimin prevalenceofbrca1andbrca2genemutationsinchinesepatientswithhighriskbreastcancer |