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Intraperitoneal cancer-immune microenvironment promotes peritoneal dissemination of gastric cancer
A solid tumor consists of cancer and stromal cells, which comprise the tumor microenvironment (TME). Tumor-associated macrophages (TAMs) are usually abundant in the TME, contributing to tumor progression. In cases of peritoneal dissemination of gastric cancer (GC), the contribution of intraperitonea...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6844331/ https://www.ncbi.nlm.nih.gov/pubmed/31741772 http://dx.doi.org/10.1080/2162402X.2019.1671760 |
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author | Sakamoto, Shuichi Kagawa, Shunsuke Kuwada, Kazuya Ito, Atene Kajioka, Hiroki Kakiuchi, Yoshihiko Watanabe, Megumi Kagawa, Tetsuya Yoshida, Ryuichi Kikuchi, Satoru Kuroda, Shinji Tazawa, Hiroshi Fujiwara, Toshiyoshi |
author_facet | Sakamoto, Shuichi Kagawa, Shunsuke Kuwada, Kazuya Ito, Atene Kajioka, Hiroki Kakiuchi, Yoshihiko Watanabe, Megumi Kagawa, Tetsuya Yoshida, Ryuichi Kikuchi, Satoru Kuroda, Shinji Tazawa, Hiroshi Fujiwara, Toshiyoshi |
author_sort | Sakamoto, Shuichi |
collection | PubMed |
description | A solid tumor consists of cancer and stromal cells, which comprise the tumor microenvironment (TME). Tumor-associated macrophages (TAMs) are usually abundant in the TME, contributing to tumor progression. In cases of peritoneal dissemination of gastric cancer (GC), the contribution of intraperitoneal TAMs remains unclear. Macrophages from peritoneal washings of GC patients were analyzed, and the link between intraperitoneal TAMs and GC cells was investigated to clarify the interaction between them in peritoneal dissemination. Macrophages were predominant among leukocytes constituting the microenvironment of the peritoneal cavity. The proportion of CD163-positive TAMs was significantly higher in stage IV than in stage I GC. Co-culture with TAMs potentiated migration and invasion of GC. IL-6 was the most increased in the medium of in vitro co-culture of macrophages and GC, and IL-6 elevation was also observed in the peritoneal washes with peritoneal dissemination. An elevated concentration of intraperitoneal IL-6 was correlated with a poor prognosis in clinical cases. In conclusion, intraperitoneal TAMs are involved in promoting peritoneal dissemination of GC via secreted IL-6. TAM-derived IL-6 could be a potential therapeutic target for peritoneal dissemination of GC. |
format | Online Article Text |
id | pubmed-6844331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-68443312019-11-18 Intraperitoneal cancer-immune microenvironment promotes peritoneal dissemination of gastric cancer Sakamoto, Shuichi Kagawa, Shunsuke Kuwada, Kazuya Ito, Atene Kajioka, Hiroki Kakiuchi, Yoshihiko Watanabe, Megumi Kagawa, Tetsuya Yoshida, Ryuichi Kikuchi, Satoru Kuroda, Shinji Tazawa, Hiroshi Fujiwara, Toshiyoshi Oncoimmunology Original Research A solid tumor consists of cancer and stromal cells, which comprise the tumor microenvironment (TME). Tumor-associated macrophages (TAMs) are usually abundant in the TME, contributing to tumor progression. In cases of peritoneal dissemination of gastric cancer (GC), the contribution of intraperitoneal TAMs remains unclear. Macrophages from peritoneal washings of GC patients were analyzed, and the link between intraperitoneal TAMs and GC cells was investigated to clarify the interaction between them in peritoneal dissemination. Macrophages were predominant among leukocytes constituting the microenvironment of the peritoneal cavity. The proportion of CD163-positive TAMs was significantly higher in stage IV than in stage I GC. Co-culture with TAMs potentiated migration and invasion of GC. IL-6 was the most increased in the medium of in vitro co-culture of macrophages and GC, and IL-6 elevation was also observed in the peritoneal washes with peritoneal dissemination. An elevated concentration of intraperitoneal IL-6 was correlated with a poor prognosis in clinical cases. In conclusion, intraperitoneal TAMs are involved in promoting peritoneal dissemination of GC via secreted IL-6. TAM-derived IL-6 could be a potential therapeutic target for peritoneal dissemination of GC. Taylor & Francis 2019-10-22 /pmc/articles/PMC6844331/ /pubmed/31741772 http://dx.doi.org/10.1080/2162402X.2019.1671760 Text en © 2019 The Author(s). Published with license by Taylor & Francis Group, LLC. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Sakamoto, Shuichi Kagawa, Shunsuke Kuwada, Kazuya Ito, Atene Kajioka, Hiroki Kakiuchi, Yoshihiko Watanabe, Megumi Kagawa, Tetsuya Yoshida, Ryuichi Kikuchi, Satoru Kuroda, Shinji Tazawa, Hiroshi Fujiwara, Toshiyoshi Intraperitoneal cancer-immune microenvironment promotes peritoneal dissemination of gastric cancer |
title | Intraperitoneal cancer-immune microenvironment promotes peritoneal dissemination of gastric cancer |
title_full | Intraperitoneal cancer-immune microenvironment promotes peritoneal dissemination of gastric cancer |
title_fullStr | Intraperitoneal cancer-immune microenvironment promotes peritoneal dissemination of gastric cancer |
title_full_unstemmed | Intraperitoneal cancer-immune microenvironment promotes peritoneal dissemination of gastric cancer |
title_short | Intraperitoneal cancer-immune microenvironment promotes peritoneal dissemination of gastric cancer |
title_sort | intraperitoneal cancer-immune microenvironment promotes peritoneal dissemination of gastric cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6844331/ https://www.ncbi.nlm.nih.gov/pubmed/31741772 http://dx.doi.org/10.1080/2162402X.2019.1671760 |
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