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Distinct clinicopathological and genomic features in solid and basaloid adenoid cystic carcinoma of the breast

Adenoid cystic carcinoma (AdCC) of the breast is a rare indolent carcinoma of salivary gland-type tumors, frequently associated with MYB genetic alteration. Solid and basaloid adenoid cystic carcinoma (SB-AdCC) is considered a sparse variant of AdCC. This study sought to search for clinicopathologic...

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Autores principales: Ji, Juan, Zhang, Fang, Duan, Fanglei, Yang, Hong, Hou, Jun, Liu, Yang, Dai, Jie, Liao, Qiong, Chen, Xian, Liu, Qingsong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120443/
https://www.ncbi.nlm.nih.gov/pubmed/35590093
http://dx.doi.org/10.1038/s41598-022-12583-w
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author Ji, Juan
Zhang, Fang
Duan, Fanglei
Yang, Hong
Hou, Jun
Liu, Yang
Dai, Jie
Liao, Qiong
Chen, Xian
Liu, Qingsong
author_facet Ji, Juan
Zhang, Fang
Duan, Fanglei
Yang, Hong
Hou, Jun
Liu, Yang
Dai, Jie
Liao, Qiong
Chen, Xian
Liu, Qingsong
author_sort Ji, Juan
collection PubMed
description Adenoid cystic carcinoma (AdCC) of the breast is a rare indolent carcinoma of salivary gland-type tumors, frequently associated with MYB genetic alteration. Solid and basaloid adenoid cystic carcinoma (SB-AdCC) is considered a sparse variant of AdCC. This study sought to search for clinicopathological and genomic features in SB-AdCC. Registered clinicopathological data on a cohort of 13 AdCC of the breast cases, including six conventional adenoid cystic carcinoma (C-AdCC) cases and seven SB-AdCC cases, were collected. MYB gene rearrangement via fluorescent in situ hybridization was investigated and MYB protein expression was evaluated by immunohistochemistry. Compared with C-AdCC, we found that the distribution of SB-AdCC cases were shifted to older age and were more frequently distant metastasis. Moreover, metastasis cases also showed a high (exceed 30%) Ki-67 index. Both groups showed MYB rearrangements and MYB protein expression, but they were less frequent in SB-AdCC than C-AdCC. To conclude, our results suggest that SB-AdCC is an aggressive variant of mammary AdCC with a higher incidence of distant metastases compared with C-AdCC, though they share common molecular features. A high Ki-67 index may be an adverse prognostic factor for metastasis.
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spelling pubmed-91204432022-05-21 Distinct clinicopathological and genomic features in solid and basaloid adenoid cystic carcinoma of the breast Ji, Juan Zhang, Fang Duan, Fanglei Yang, Hong Hou, Jun Liu, Yang Dai, Jie Liao, Qiong Chen, Xian Liu, Qingsong Sci Rep Article Adenoid cystic carcinoma (AdCC) of the breast is a rare indolent carcinoma of salivary gland-type tumors, frequently associated with MYB genetic alteration. Solid and basaloid adenoid cystic carcinoma (SB-AdCC) is considered a sparse variant of AdCC. This study sought to search for clinicopathological and genomic features in SB-AdCC. Registered clinicopathological data on a cohort of 13 AdCC of the breast cases, including six conventional adenoid cystic carcinoma (C-AdCC) cases and seven SB-AdCC cases, were collected. MYB gene rearrangement via fluorescent in situ hybridization was investigated and MYB protein expression was evaluated by immunohistochemistry. Compared with C-AdCC, we found that the distribution of SB-AdCC cases were shifted to older age and were more frequently distant metastasis. Moreover, metastasis cases also showed a high (exceed 30%) Ki-67 index. Both groups showed MYB rearrangements and MYB protein expression, but they were less frequent in SB-AdCC than C-AdCC. To conclude, our results suggest that SB-AdCC is an aggressive variant of mammary AdCC with a higher incidence of distant metastases compared with C-AdCC, though they share common molecular features. A high Ki-67 index may be an adverse prognostic factor for metastasis. Nature Publishing Group UK 2022-05-19 /pmc/articles/PMC9120443/ /pubmed/35590093 http://dx.doi.org/10.1038/s41598-022-12583-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Ji, Juan
Zhang, Fang
Duan, Fanglei
Yang, Hong
Hou, Jun
Liu, Yang
Dai, Jie
Liao, Qiong
Chen, Xian
Liu, Qingsong
Distinct clinicopathological and genomic features in solid and basaloid adenoid cystic carcinoma of the breast
title Distinct clinicopathological and genomic features in solid and basaloid adenoid cystic carcinoma of the breast
title_full Distinct clinicopathological and genomic features in solid and basaloid adenoid cystic carcinoma of the breast
title_fullStr Distinct clinicopathological and genomic features in solid and basaloid adenoid cystic carcinoma of the breast
title_full_unstemmed Distinct clinicopathological and genomic features in solid and basaloid adenoid cystic carcinoma of the breast
title_short Distinct clinicopathological and genomic features in solid and basaloid adenoid cystic carcinoma of the breast
title_sort distinct clinicopathological and genomic features in solid and basaloid adenoid cystic carcinoma of the breast
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120443/
https://www.ncbi.nlm.nih.gov/pubmed/35590093
http://dx.doi.org/10.1038/s41598-022-12583-w
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