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B Cells in Breast Cancer Pathology

SIMPLE SUMMARY: B cells in the tumour microenvironment and lymph nodes have affirmed their role in breast cancer pathology. Multiplex imaging, single cell, and spatial transcriptomics of cancer patients’ breast carcinomas and lymph nodes have illustrated the diversity and spatial context of B cells...

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Autores principales: Li, Mengyuan, Quintana, Angela, Alberts, Elena, Hung, Miu Shing, Boulat, Victoire, Ripoll, Mercè Martí, Grigoriadis, Anita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000926/
https://www.ncbi.nlm.nih.gov/pubmed/36900307
http://dx.doi.org/10.3390/cancers15051517
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author Li, Mengyuan
Quintana, Angela
Alberts, Elena
Hung, Miu Shing
Boulat, Victoire
Ripoll, Mercè Martí
Grigoriadis, Anita
author_facet Li, Mengyuan
Quintana, Angela
Alberts, Elena
Hung, Miu Shing
Boulat, Victoire
Ripoll, Mercè Martí
Grigoriadis, Anita
author_sort Li, Mengyuan
collection PubMed
description SIMPLE SUMMARY: B cells in the tumour microenvironment and lymph nodes have affirmed their role in breast cancer pathology. Multiplex imaging, single cell, and spatial transcriptomics of cancer patients’ breast carcinomas and lymph nodes have illustrated the diversity and spatial context of B cells in this disease. Their anti-tumoural and pro-tumoural functions make B cells an attractive research area to improve chemo- and immuno-therapy responses for breast cancer patients. ABSTRACT: B cells have recently become a focus in breast cancer pathology due to their influence on tumour regression, prognosis, and response to treatment, besides their contribution to antigen presentation, immunoglobulin production, and regulation of adaptive responses. As our understanding of diverse B cell subsets in eliciting both pro- and anti-inflammatory responses in breast cancer patients increases, it has become pertinent to address the molecular and clinical relevance of these immune cell populations within the tumour microenvironment (TME). At the primary tumour site, B cells are either found spatially dispersed or aggregated in so-called tertiary lymphoid structures (TLS). In axillary lymph nodes (LNs), B cell populations, amongst a plethora of activities, undergo germinal centre reactions to ensure humoral immunity. With the recent approval for the addition of immunotherapeutic drugs as a treatment option in the early and metastatic settings for triple-negative breast cancer (TNBC) patients, B cell populations or TLS may resemble valuable biomarkers for immunotherapy responses in certain breast cancer subgroups. New technologies such as spatially defined sequencing techniques, multiplex imaging, and digital technologies have further deciphered the diversity of B cells and the morphological structures in which they appear in the tumour and LNs. Thus, in this review, we comprehensively summarise the current knowledge of B cells in breast cancer. In addition, we provide a user-friendly single-cell RNA-sequencing platform, called “B singLe cEll rna-Seq browSer” (BLESS) platform, with a focus on the B cells in breast cancer patients to interrogate the latest publicly available single-cell RNA-sequencing data collected from diverse breast cancer studies. Finally, we explore their clinical relevance as biomarkers or molecular targets for future interventions.
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spelling pubmed-100009262023-03-11 B Cells in Breast Cancer Pathology Li, Mengyuan Quintana, Angela Alberts, Elena Hung, Miu Shing Boulat, Victoire Ripoll, Mercè Martí Grigoriadis, Anita Cancers (Basel) Review SIMPLE SUMMARY: B cells in the tumour microenvironment and lymph nodes have affirmed their role in breast cancer pathology. Multiplex imaging, single cell, and spatial transcriptomics of cancer patients’ breast carcinomas and lymph nodes have illustrated the diversity and spatial context of B cells in this disease. Their anti-tumoural and pro-tumoural functions make B cells an attractive research area to improve chemo- and immuno-therapy responses for breast cancer patients. ABSTRACT: B cells have recently become a focus in breast cancer pathology due to their influence on tumour regression, prognosis, and response to treatment, besides their contribution to antigen presentation, immunoglobulin production, and regulation of adaptive responses. As our understanding of diverse B cell subsets in eliciting both pro- and anti-inflammatory responses in breast cancer patients increases, it has become pertinent to address the molecular and clinical relevance of these immune cell populations within the tumour microenvironment (TME). At the primary tumour site, B cells are either found spatially dispersed or aggregated in so-called tertiary lymphoid structures (TLS). In axillary lymph nodes (LNs), B cell populations, amongst a plethora of activities, undergo germinal centre reactions to ensure humoral immunity. With the recent approval for the addition of immunotherapeutic drugs as a treatment option in the early and metastatic settings for triple-negative breast cancer (TNBC) patients, B cell populations or TLS may resemble valuable biomarkers for immunotherapy responses in certain breast cancer subgroups. New technologies such as spatially defined sequencing techniques, multiplex imaging, and digital technologies have further deciphered the diversity of B cells and the morphological structures in which they appear in the tumour and LNs. Thus, in this review, we comprehensively summarise the current knowledge of B cells in breast cancer. In addition, we provide a user-friendly single-cell RNA-sequencing platform, called “B singLe cEll rna-Seq browSer” (BLESS) platform, with a focus on the B cells in breast cancer patients to interrogate the latest publicly available single-cell RNA-sequencing data collected from diverse breast cancer studies. Finally, we explore their clinical relevance as biomarkers or molecular targets for future interventions. MDPI 2023-02-28 /pmc/articles/PMC10000926/ /pubmed/36900307 http://dx.doi.org/10.3390/cancers15051517 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Li, Mengyuan
Quintana, Angela
Alberts, Elena
Hung, Miu Shing
Boulat, Victoire
Ripoll, Mercè Martí
Grigoriadis, Anita
B Cells in Breast Cancer Pathology
title B Cells in Breast Cancer Pathology
title_full B Cells in Breast Cancer Pathology
title_fullStr B Cells in Breast Cancer Pathology
title_full_unstemmed B Cells in Breast Cancer Pathology
title_short B Cells in Breast Cancer Pathology
title_sort b cells in breast cancer pathology
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10000926/
https://www.ncbi.nlm.nih.gov/pubmed/36900307
http://dx.doi.org/10.3390/cancers15051517
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