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Sexual dimorphism in gastric cancer: tumor-associated neutrophils predict patient outcome only for women
PURPOSE: Tumor-associated neutrophils (TANs) are part of the tumor immune microenvironment (TIME) and may contribute to gastric cancer (GC) biology. We hypothesized that TAN are enriched in the TIME, show sex-specific differences, and correlate with patient outcome. METHODS: We analyzed the distribu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942031/ https://www.ncbi.nlm.nih.gov/pubmed/31741042 http://dx.doi.org/10.1007/s00432-019-03082-z |
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author | Clausen, Franziska Behrens, Hans-Michael Krüger, Sandra Röcken, Christoph |
author_facet | Clausen, Franziska Behrens, Hans-Michael Krüger, Sandra Röcken, Christoph |
author_sort | Clausen, Franziska |
collection | PubMed |
description | PURPOSE: Tumor-associated neutrophils (TANs) are part of the tumor immune microenvironment (TIME) and may contribute to gastric cancer (GC) biology. We hypothesized that TAN are enriched in the TIME, show sex-specific differences, and correlate with patient outcome. METHODS: We analyzed the distribution and putative tumor biological significance of TANs in a well-characterized, therapy-naïve, European GC cohort using immunohistochemical staining of myeloperoxidase (MPO), and digital image analysis using Definiens Tissue Studio(®). RESULTS: Different tumor compartments were examined, and TAN densities were correlated with various clinicopathological patient characteristics. TAN density showed a large interindividual variability ranging from 0 to 6711.0 TANs/mm(2). Intratumoral distribution patterns were inhomogeneous (tumor surface vs. tumor center vs. invasion front) and correlated significantly with Laurén phenotype, tumor grade, and microsatellite status in the tumor center and invasion front. In the multivariate analysis, TAN density in the invasion front was an independent predictor of tumor-specific survival only for women (HR = 2.77, p < 0.001). In men, no correlation was found between TAN density and survival. CONCLUSION: With regard to TANs, our study independently validates sexual dimorphism in GC biology. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00432-019-03082-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6942031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-69420312020-01-16 Sexual dimorphism in gastric cancer: tumor-associated neutrophils predict patient outcome only for women Clausen, Franziska Behrens, Hans-Michael Krüger, Sandra Röcken, Christoph J Cancer Res Clin Oncol Original Article – Cancer Research PURPOSE: Tumor-associated neutrophils (TANs) are part of the tumor immune microenvironment (TIME) and may contribute to gastric cancer (GC) biology. We hypothesized that TAN are enriched in the TIME, show sex-specific differences, and correlate with patient outcome. METHODS: We analyzed the distribution and putative tumor biological significance of TANs in a well-characterized, therapy-naïve, European GC cohort using immunohistochemical staining of myeloperoxidase (MPO), and digital image analysis using Definiens Tissue Studio(®). RESULTS: Different tumor compartments were examined, and TAN densities were correlated with various clinicopathological patient characteristics. TAN density showed a large interindividual variability ranging from 0 to 6711.0 TANs/mm(2). Intratumoral distribution patterns were inhomogeneous (tumor surface vs. tumor center vs. invasion front) and correlated significantly with Laurén phenotype, tumor grade, and microsatellite status in the tumor center and invasion front. In the multivariate analysis, TAN density in the invasion front was an independent predictor of tumor-specific survival only for women (HR = 2.77, p < 0.001). In men, no correlation was found between TAN density and survival. CONCLUSION: With regard to TANs, our study independently validates sexual dimorphism in GC biology. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00432-019-03082-z) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-11-19 2020 /pmc/articles/PMC6942031/ /pubmed/31741042 http://dx.doi.org/10.1007/s00432-019-03082-z Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article – Cancer Research Clausen, Franziska Behrens, Hans-Michael Krüger, Sandra Röcken, Christoph Sexual dimorphism in gastric cancer: tumor-associated neutrophils predict patient outcome only for women |
title | Sexual dimorphism in gastric cancer: tumor-associated neutrophils predict patient outcome only for women |
title_full | Sexual dimorphism in gastric cancer: tumor-associated neutrophils predict patient outcome only for women |
title_fullStr | Sexual dimorphism in gastric cancer: tumor-associated neutrophils predict patient outcome only for women |
title_full_unstemmed | Sexual dimorphism in gastric cancer: tumor-associated neutrophils predict patient outcome only for women |
title_short | Sexual dimorphism in gastric cancer: tumor-associated neutrophils predict patient outcome only for women |
title_sort | sexual dimorphism in gastric cancer: tumor-associated neutrophils predict patient outcome only for women |
topic | Original Article – Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942031/ https://www.ncbi.nlm.nih.gov/pubmed/31741042 http://dx.doi.org/10.1007/s00432-019-03082-z |
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