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Brief report: Lymph node morphology in stage II colorectal cancer
BACKGROUND: Colorectal cancer is one of the leading causes of cancer-associated morbidity and mortality worldwide. The local anti-tumour immune response is particularly important for patients with stage II where the tumour-draining lymph nodes have not yet succumbed to tumour spread. The lymph nodes...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007027/ https://www.ncbi.nlm.nih.gov/pubmed/33780511 http://dx.doi.org/10.1371/journal.pone.0249197 |
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author | Greenwood, Annabelle Keating, John Kenwright, Diane Shekouh, Ali Dalzell, Alex Dennett, Elizabeth Danielson, Kirsty |
author_facet | Greenwood, Annabelle Keating, John Kenwright, Diane Shekouh, Ali Dalzell, Alex Dennett, Elizabeth Danielson, Kirsty |
author_sort | Greenwood, Annabelle |
collection | PubMed |
description | BACKGROUND: Colorectal cancer is one of the leading causes of cancer-associated morbidity and mortality worldwide. The local anti-tumour immune response is particularly important for patients with stage II where the tumour-draining lymph nodes have not yet succumbed to tumour spread. The lymph nodes allow for the expansion and release of B cell compartments such as primary follicles and germinal centres. A variation in this anti-tumour immune response may influence the observed clinical heterogeneity in stage II patients. AIM: The aim of this study was to explore tumour-draining lymph node histomorphological changes and tumour pathological risk factors including the immunomodulatory microRNA-21 (miR-21) in a small cohort of stage II CRC. METHODS: A total of 23 stage II colorectal cancer patients were included. Tumour and normal mucosa samples were analysed for miR-21 expression levels and B-cell compartments were quantified from Haematoxylin and Eosin slides of lymph nodes. These measures were compared to clinicopathological risk factors such as perforation, bowel obstruction, T4 stage and high-grade. RESULTS: We observed greater Follicle density in patients with a lower tumour T stage and higher germinal centre density in patients with higher pre-operative carcinoembryonic antigen levels. Trends were also detected between tumours with deficiency in mismatch repair proteins, lymphatic invasion and both the density and size of B-cell compartments. Lastly, elevated tumour miR-21 was associated with decreased Follicle and germinal centre size. CONCLUSION: Variation in B-cell compartments of tumour-draining lymph nodes is associated with clinicopathological risk factors in stage II CRC patients. |
format | Online Article Text |
id | pubmed-8007027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-80070272021-04-07 Brief report: Lymph node morphology in stage II colorectal cancer Greenwood, Annabelle Keating, John Kenwright, Diane Shekouh, Ali Dalzell, Alex Dennett, Elizabeth Danielson, Kirsty PLoS One Research Article BACKGROUND: Colorectal cancer is one of the leading causes of cancer-associated morbidity and mortality worldwide. The local anti-tumour immune response is particularly important for patients with stage II where the tumour-draining lymph nodes have not yet succumbed to tumour spread. The lymph nodes allow for the expansion and release of B cell compartments such as primary follicles and germinal centres. A variation in this anti-tumour immune response may influence the observed clinical heterogeneity in stage II patients. AIM: The aim of this study was to explore tumour-draining lymph node histomorphological changes and tumour pathological risk factors including the immunomodulatory microRNA-21 (miR-21) in a small cohort of stage II CRC. METHODS: A total of 23 stage II colorectal cancer patients were included. Tumour and normal mucosa samples were analysed for miR-21 expression levels and B-cell compartments were quantified from Haematoxylin and Eosin slides of lymph nodes. These measures were compared to clinicopathological risk factors such as perforation, bowel obstruction, T4 stage and high-grade. RESULTS: We observed greater Follicle density in patients with a lower tumour T stage and higher germinal centre density in patients with higher pre-operative carcinoembryonic antigen levels. Trends were also detected between tumours with deficiency in mismatch repair proteins, lymphatic invasion and both the density and size of B-cell compartments. Lastly, elevated tumour miR-21 was associated with decreased Follicle and germinal centre size. CONCLUSION: Variation in B-cell compartments of tumour-draining lymph nodes is associated with clinicopathological risk factors in stage II CRC patients. Public Library of Science 2021-03-29 /pmc/articles/PMC8007027/ /pubmed/33780511 http://dx.doi.org/10.1371/journal.pone.0249197 Text en © 2021 Greenwood et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Greenwood, Annabelle Keating, John Kenwright, Diane Shekouh, Ali Dalzell, Alex Dennett, Elizabeth Danielson, Kirsty Brief report: Lymph node morphology in stage II colorectal cancer |
title | Brief report: Lymph node morphology in stage II colorectal cancer |
title_full | Brief report: Lymph node morphology in stage II colorectal cancer |
title_fullStr | Brief report: Lymph node morphology in stage II colorectal cancer |
title_full_unstemmed | Brief report: Lymph node morphology in stage II colorectal cancer |
title_short | Brief report: Lymph node morphology in stage II colorectal cancer |
title_sort | brief report: lymph node morphology in stage ii colorectal cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007027/ https://www.ncbi.nlm.nih.gov/pubmed/33780511 http://dx.doi.org/10.1371/journal.pone.0249197 |
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