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本文引用的文献

1
Molecular-Targeted Immunotherapeutic Strategy for Melanoma via Dual-Targeting Nanoparticles Delivering Small Interfering RNA to Tumor-Associated Macrophages.通过向肿瘤相关巨噬细胞递送小干扰 RNA 的双靶向纳米粒子实现黑色素瘤的分子靶向免疫治疗策略。
ACS Nano. 2017 Sep 26;11(9):9536-9549. doi: 10.1021/acsnano.7b05465. Epub 2017 Sep 6.
2
Targeting macrophage anti-tumor activity to suppress melanoma progression.靶向巨噬细胞的抗肿瘤活性以抑制黑色素瘤进展。
Oncotarget. 2017 Mar 14;8(11):18486-18496. doi: 10.18632/oncotarget.14474.
3
Downregulation of sphingosine kinase-1 induces protective tumor immunity by promoting M1 macrophage response in melanoma.鞘氨醇激酶-1的下调通过促进黑色素瘤中的M1巨噬细胞反应诱导保护性肿瘤免疫。
Oncotarget. 2016 Nov 1;7(44):71873-71886. doi: 10.18632/oncotarget.12380.
4
Tumour hypoxia promotes melanoma growth and metastasis via High Mobility Group Box-1 and M2-like macrophages.肿瘤缺氧通过高迁移率族蛋白 B1 和 M2 样巨噬细胞促进黑色素瘤生长和转移。
Sci Rep. 2016 Jul 18;6:29914. doi: 10.1038/srep29914.
5
The Multifaceted Role of Perivascular Macrophages in Tumors.肿瘤中血管周围巨噬细胞的多方面作用
Cancer Cell. 2016 Jul 11;30(1):18-25. doi: 10.1016/j.ccell.2016.05.017.
6
MFG-E8 Drives Melanoma Growth by Stimulating Mesenchymal Stromal Cell-Induced Angiogenesis and M2 Polarization of Tumor-Associated Macrophages.MFG-E8通过刺激间充质基质细胞诱导的血管生成和肿瘤相关巨噬细胞的M2极化来驱动黑色素瘤生长。
Cancer Res. 2016 Jul 15;76(14):4283-92. doi: 10.1158/0008-5472.CAN-15-2812. Epub 2016 May 17.
7
Renalase Expression by Melanoma and Tumor-Associated Macrophages Promotes Tumor Growth through a STAT3-Mediated Mechanism.黑色素瘤和肿瘤相关巨噬细胞中的肾酶表达通过STAT3介导的机制促进肿瘤生长。
Cancer Res. 2016 Jul 1;76(13):3884-94. doi: 10.1158/0008-5472.CAN-15-1524. Epub 2016 May 9.
8
Investigating associations of cyclooxygenase-2 expression with angiogenesis, proliferation, macrophage and T-lymphocyte infiltration in canine melanocytic tumours.研究犬黑素细胞瘤中环氧合酶-2表达与血管生成、增殖、巨噬细胞及T淋巴细胞浸润的相关性。
Melanoma Res. 2016 Aug;26(4):338-47. doi: 10.1097/CMR.0000000000000262.
9
The Basis of Oncoimmunology.肿瘤免疫学基础。
Cell. 2016 Mar 10;164(6):1233-1247. doi: 10.1016/j.cell.2016.01.049.
10
[Immune checkpoint‑targeted cancer immunotherapies].[免疫检查点靶向癌症免疫疗法]
Postepy Hig Med Dosw (Online). 2016 Jan 26;70:25-42. doi: 10.5604/17322693.1192926.

皮肤黑色素瘤中的巨噬细胞——黑色素瘤发生的关键要素。

Macrophages in skin melanoma-the key element in melanomagenesis.

作者信息

Pieniazek Malgorzata, Matkowski Rafal, Donizy Piotr

机构信息

Department of Clinical Oncology, Tadeusz Koszarowski Regional Oncology Centre, Opole 45-061, Poland.

Department of Oncology and Division of Surgical Oncology, Wroclaw Medical University, Wroclaw 50-367, Poland.

出版信息

Oncol Lett. 2018 Apr;15(4):5399-5404. doi: 10.3892/ol.2018.8021. Epub 2018 Feb 9.

DOI:10.3892/ol.2018.8021
PMID:29552183
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5840697/
Abstract

Cutaneous melanoma is an aggressive cancer and its onset and growth are associated, through direct and indirect interactions, with the cancer microenvironment. The microenvironment comprises a dynamic complex of numerous types of cells (due to histogenesis) that constantly interact with each other through multiple cytokines and signaling proteins. Macrophages are one of the most thoroughly studied pleiotropic cells of the immune system. One of their major cytophysiological functions is their involvement in phagocytosis. Previous studies examining the microenvironment of melanomas and tumor-associated macrophages have revealed that they are involved in all stages of melanomagenesis. In the case of cancer initiation, they form an inflammatory microenvironment and then suppress the anticancer activity of the immune system, stimulate angiogenesis, enhance migration and invasion of the cancer cells, and ultimately contribute to the metastatic process. The present review provides a detailed overview on the function of macrophages in the melanoma microenvironment.

摘要

皮肤黑色素瘤是一种侵袭性癌症,其发生和生长通过直接和间接相互作用与癌症微环境相关。微环境由多种类型细胞(由于组织发生)组成的动态复合体构成,这些细胞通过多种细胞因子和信号蛋白不断相互作用。巨噬细胞是免疫系统中研究最深入的多能细胞之一。它们的主要细胞生理功能之一是参与吞噬作用。先前研究黑色素瘤微环境和肿瘤相关巨噬细胞发现,它们参与黑色素瘤发生的各个阶段。在癌症起始阶段,它们形成炎症微环境,然后抑制免疫系统的抗癌活性,刺激血管生成,增强癌细胞的迁移和侵袭,最终促成转移过程。本综述详细概述了巨噬细胞在黑色素瘤微环境中的功能。