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A Molecular and Morphological Deep-Dive Into Metaplastic Breast Cancers

Metaplastic breast cancers (MBC) are relatively rare but account for significant global breast cancer mortality. Typically presenting without oestrogen and progesterone receptors or HER2 expression, these triple negative breast cancers are the archetypal ‘stem cell-like’ tumours that show a variety...

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Detalles Bibliográficos
Autores principales: McCart Reed, Amy E, Lakhani, Sunil R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535896/
https://www.ncbi.nlm.nih.gov/pubmed/31205411
http://dx.doi.org/10.1177/1176935119850155
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author McCart Reed, Amy E
Lakhani, Sunil R
author_facet McCart Reed, Amy E
Lakhani, Sunil R
author_sort McCart Reed, Amy E
collection PubMed
description Metaplastic breast cancers (MBC) are relatively rare but account for significant global breast cancer mortality. Typically presenting without oestrogen and progesterone receptors or HER2 expression, these triple negative breast cancers are the archetypal ‘stem cell-like’ tumours that show a variety of metaplastic elements, including squamous, spindle, and chondroid. Given the vast heterogeneity in MBC by definition, large cohort studies are needed to draw conclusions. Together with our consortium colleagues, a cohort of 347 MBC was established, and a detailed morphological assessment made in an effort to understand the clinical relevance of the current diagnostic guidelines. Biomarker expression was investigated, and whole exome sequencing was performed. Herein, we provide an overview and contextualisation of the study.
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spelling pubmed-65358962019-06-14 A Molecular and Morphological Deep-Dive Into Metaplastic Breast Cancers McCart Reed, Amy E Lakhani, Sunil R Cancer Inform Article Commentary Metaplastic breast cancers (MBC) are relatively rare but account for significant global breast cancer mortality. Typically presenting without oestrogen and progesterone receptors or HER2 expression, these triple negative breast cancers are the archetypal ‘stem cell-like’ tumours that show a variety of metaplastic elements, including squamous, spindle, and chondroid. Given the vast heterogeneity in MBC by definition, large cohort studies are needed to draw conclusions. Together with our consortium colleagues, a cohort of 347 MBC was established, and a detailed morphological assessment made in an effort to understand the clinical relevance of the current diagnostic guidelines. Biomarker expression was investigated, and whole exome sequencing was performed. Herein, we provide an overview and contextualisation of the study. SAGE Publications 2019-05-17 /pmc/articles/PMC6535896/ /pubmed/31205411 http://dx.doi.org/10.1177/1176935119850155 Text en © The Author(s) 2019 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Article Commentary
McCart Reed, Amy E
Lakhani, Sunil R
A Molecular and Morphological Deep-Dive Into Metaplastic Breast Cancers
title A Molecular and Morphological Deep-Dive Into Metaplastic Breast Cancers
title_full A Molecular and Morphological Deep-Dive Into Metaplastic Breast Cancers
title_fullStr A Molecular and Morphological Deep-Dive Into Metaplastic Breast Cancers
title_full_unstemmed A Molecular and Morphological Deep-Dive Into Metaplastic Breast Cancers
title_short A Molecular and Morphological Deep-Dive Into Metaplastic Breast Cancers
title_sort molecular and morphological deep-dive into metaplastic breast cancers
topic Article Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6535896/
https://www.ncbi.nlm.nih.gov/pubmed/31205411
http://dx.doi.org/10.1177/1176935119850155
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