国际肿瘤学杂志 ›› 2017, Vol. 44 ›› Issue (12): 940-943.doi: 10.3760/cma.j.issn.1673-422X.2017.12.015

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巨噬细胞调控肝脏微环境在消化系统肿瘤肝转移中的 作用及机制

肖华,刘武   

  1. 410013 长沙, 湖南省肿瘤医院 中南大学湘雅医学院附属肿瘤医院胃十二指肠胰腺外科(肖华),消化泌尿内科(刘武)
  • 出版日期:2017-12-08 发布日期:2017-12-01
  • 通讯作者: 肖华,Email: huakexh2010@163.com E-mail:huakexh2010@163.com
  • 基金资助:
    湖南省卫生计生委2017年度科研计划(B2017101)

Role and mechanism of macrophages modulating the liver microenvironment in digestive tract malignancies liver metastasis

Xiao Hua, Liu Wu.   

  1. Department of Gastroduodenal and Pancreatic Surgery, Hunan Cancer Hospital & Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, Changsha 410013, China
  • Online:2017-12-08 Published:2017-12-01
  • Contact: Xiao Hua, Email: huakexh2010@163.com E-mail:huakexh2010@163.com
  • Supported by:
    2017 Annual Research Project of Health and Family Planning Commission of Hunan Province of China (B2017101)

摘要: 巨噬细胞作为肝脏微环境的重要组成部分,在消化系统肿瘤肝转移的发生、发展中起重要作用。一方面巨噬细胞与肝窦内皮细胞等构成肝脏第一道防线,能够吞噬进入肝血窦的循环肿瘤细胞或促进其凋亡,或者发挥细胞毒性作用从而抑制肝转移的发生。另一方面,巨噬细胞与循环肿瘤细胞结合以后活化,释放肝细胞生长因子等多种细胞因子,刺激肿瘤细胞的增殖进而促进肝转移的发生。针对巨噬细胞开展肿瘤免疫治疗,或许可以为消化系统肿瘤肝转移的防治提供新的思路。

关键词: 巨噬细胞, 肿瘤转移, 肿瘤微环境

Abstract: Macrophagses are important components of the liver microenvironment, and play an essential role in the occurrence and development of liver metastasis of digestive system malignancies. Macrophages and liver sinusoidal endothelial cells constitute the first defense line of the liver, which can rapidly recognize and arrest the circulating tumor cells invading into the liver sinusoidal, by phagocytosis or promoting their apoptosis, thus play a cytotoxic effect to inhibit the occurrence of liver metastases. On the other hand, macrophages can combine to the circulating tumor cells and be activated. As a result, hepatocyte growth factor and other cytokines were released, which significantly promoted the proliferation of tumors cells, and thus promoting liver metastases. It may provide a new idea in preventing and treating liver metastasis of digestive system malignancies by targeting macrophages during tumor immunotherapy

Key words: Macrophages, Neoplasm metastasis, Tumor microenvironment