肿瘤微环境
糖酵解
肿瘤进展
免疫系统
生物
新陈代谢
癌症研究
细胞生物学
一氧化氮
活性氧
重编程
化学
细胞
生物化学
免疫学
内分泌学
基因
作者
Romana T. Netea‐Maier,Johannes W. A. Smit,Mihai G. Netea
出处
期刊:Cancer Letters
[Elsevier]
日期:2017-10-27
卷期号:413: 102-109
被引量:273
标识
DOI:10.1016/j.canlet.2017.10.037
摘要
In order to adapt to the reduced availability of nutrients and oxygen in the tumor microenvironment and the increased requirements of energy and building blocks necessary for maintaining their high proliferation rate, malignant cells undergo metabolic changes that result in an increased production of lactate, nitric oxide, reactive oxygen species, prostaglandins and other byproducts of arachidonic acid metabolism that influence both the composition of the inflammatory microenvironment and the function of the tumor-associated macrophages (TAMs). In response to cues present in the TME, among which products of altered tumor cell metabolism, TAMs are also required to reprogram their metabolism, with activation of glycolysis, fatty acid synthesis and altered nitrogen cycle metabolism. These changes result in functional reprogramming of TAMs which includes changes in the production of cytokines and angiogenetic factors, and contribute to the tumor progression and metastasis. Understanding the metabolic changes governing the intricate relationship between the tumor cells and the TAMs represents an essential step towards developing novel therapeutic approaches targeting the metabolic reprogramming of the immune cells to potentiate their tumoricidal potential and to circumvent therapy resistance.
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