Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Clausen, Franziska, Behrens, Hans-Michael, Krüger, Sandra, Röcken, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
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
_version_ 1783484641234124800
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
work_keys_str_mv AT clausenfranziska sexualdimorphismingastriccancertumorassociatedneutrophilspredictpatientoutcomeonlyforwomen
AT behrenshansmichael sexualdimorphismingastriccancertumorassociatedneutrophilspredictpatientoutcomeonlyforwomen
AT krugersandra sexualdimorphismingastriccancertumorassociatedneutrophilspredictpatientoutcomeonlyforwomen
AT rockenchristoph sexualdimorphismingastriccancertumorassociatedneutrophilspredictpatientoutcomeonlyforwomen