Intraperitoneal cancer-immune microenvironment promotes peritoneal dissemination of gastric cancer

肿瘤微环境 腹膜腔 间质细胞 医学 免疫系统 癌症 癌症研究 腹腔注射 川地163 癌细胞 腹膜 免疫学 病理 体外 巨噬细胞 内科学 生物 解剖 生物化学
作者
Shuichi Sakamoto,Shunsuke Kagawa,Kazuya Kuwada,Atene Ito,Hiroki Kajioka,Yoshihiko Kakiuchi,Megumi Watanabe,Tetsuya Kagawa,Ryuichi Yoshida,Satoru Kikuchi,Shinji Kuroda,Hiroshi Tazawa,Toshiyoshi Fujiwara
出处
期刊:OncoImmunology [Landes Bioscience]
卷期号:8 (12): e1671760-e1671760 被引量:37
标识
DOI:10.1080/2162402x.2019.1671760
摘要

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.

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