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The disease sites of female genital cancers of BRCA1/2-associated hereditary breast and ovarian cancer: a retrospective study
Disease sites of female genital tract cancers of BRCA1/2-associated hereditary breast and ovarian cancer (HBOC) are less understood than non-hereditary cancers. We aimed to elucidate the disease site distribution of genital cancers in women with the germline BRCA1 and BRCA2 pathogenic variants (BRCA...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7856749/ https://www.ncbi.nlm.nih.gov/pubmed/33531027 http://dx.doi.org/10.1186/s12957-021-02151-3 |
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author | Mitamura, Takashi Sekine, Masayuki Arai, Masami Shibata, Yuka Kato, Momoko Yokoyama, Shiro Yamashita, Hiroko Watari, Hidemichi Yabe, Ichiro Nomura, Hiroyuki Enomoto, Takayuki Nakamura, Seigo |
author_facet | Mitamura, Takashi Sekine, Masayuki Arai, Masami Shibata, Yuka Kato, Momoko Yokoyama, Shiro Yamashita, Hiroko Watari, Hidemichi Yabe, Ichiro Nomura, Hiroyuki Enomoto, Takayuki Nakamura, Seigo |
author_sort | Mitamura, Takashi |
collection | PubMed |
description | Disease sites of female genital tract cancers of BRCA1/2-associated hereditary breast and ovarian cancer (HBOC) are less understood than non-hereditary cancers. We aimed to elucidate the disease site distribution of genital cancers in women with the germline BRCA1 and BRCA2 pathogenic variants (BRCA1+ and BRCA2+) of HBOC. For the primary disease site, the proportion of fallopian tube and peritoneal cancer was significantly higher in BRCA2+ (40.5%) compared with BRCA1+ (15.4%) and BRCA− (no pathogenic variant, 12.8%). For the metastatic site, the proportion of peritoneal dissemination was significantly higher in BRCA1+ (71.9%) than BRCA− (55.1%) and not different from BRCA2+ (71.4%). With one of the most extensive patients, this study supported the previous reports showing that the pathogenic variants of BRCA1/2 were involved in the female genitalia’s disease sites. |
format | Online Article Text |
id | pubmed-7856749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78567492021-02-04 The disease sites of female genital cancers of BRCA1/2-associated hereditary breast and ovarian cancer: a retrospective study Mitamura, Takashi Sekine, Masayuki Arai, Masami Shibata, Yuka Kato, Momoko Yokoyama, Shiro Yamashita, Hiroko Watari, Hidemichi Yabe, Ichiro Nomura, Hiroyuki Enomoto, Takayuki Nakamura, Seigo World J Surg Oncol Correspondence Disease sites of female genital tract cancers of BRCA1/2-associated hereditary breast and ovarian cancer (HBOC) are less understood than non-hereditary cancers. We aimed to elucidate the disease site distribution of genital cancers in women with the germline BRCA1 and BRCA2 pathogenic variants (BRCA1+ and BRCA2+) of HBOC. For the primary disease site, the proportion of fallopian tube and peritoneal cancer was significantly higher in BRCA2+ (40.5%) compared with BRCA1+ (15.4%) and BRCA− (no pathogenic variant, 12.8%). For the metastatic site, the proportion of peritoneal dissemination was significantly higher in BRCA1+ (71.9%) than BRCA− (55.1%) and not different from BRCA2+ (71.4%). With one of the most extensive patients, this study supported the previous reports showing that the pathogenic variants of BRCA1/2 were involved in the female genitalia’s disease sites. BioMed Central 2021-02-02 /pmc/articles/PMC7856749/ /pubmed/33531027 http://dx.doi.org/10.1186/s12957-021-02151-3 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Correspondence Mitamura, Takashi Sekine, Masayuki Arai, Masami Shibata, Yuka Kato, Momoko Yokoyama, Shiro Yamashita, Hiroko Watari, Hidemichi Yabe, Ichiro Nomura, Hiroyuki Enomoto, Takayuki Nakamura, Seigo The disease sites of female genital cancers of BRCA1/2-associated hereditary breast and ovarian cancer: a retrospective study |
title | The disease sites of female genital cancers of BRCA1/2-associated hereditary breast and ovarian cancer: a retrospective study |
title_full | The disease sites of female genital cancers of BRCA1/2-associated hereditary breast and ovarian cancer: a retrospective study |
title_fullStr | The disease sites of female genital cancers of BRCA1/2-associated hereditary breast and ovarian cancer: a retrospective study |
title_full_unstemmed | The disease sites of female genital cancers of BRCA1/2-associated hereditary breast and ovarian cancer: a retrospective study |
title_short | The disease sites of female genital cancers of BRCA1/2-associated hereditary breast and ovarian cancer: a retrospective study |
title_sort | disease sites of female genital cancers of brca1/2-associated hereditary breast and ovarian cancer: a retrospective study |
topic | Correspondence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7856749/ https://www.ncbi.nlm.nih.gov/pubmed/33531027 http://dx.doi.org/10.1186/s12957-021-02151-3 |
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