肿瘤微环境
巨噬细胞极化
免疫系统
胰腺癌
缺氧(环境)
癌症研究
生物
肿瘤进展
M2巨噬细胞
胰腺肿瘤
糖酵解
巨噬细胞
细胞生物学
新陈代谢
化学
免疫学
癌症
基因
内分泌学
生物化学
有机化学
体外
氧气
遗传学
作者
Kuldeep S. Attri,Kamiya Mehla,Pankaj K. Singh
出处
期刊:Methods in molecular biology
日期:2018-01-01
卷期号:: 265-276
被引量:17
标识
DOI:10.1007/978-1-4939-7665-2_23
摘要
Hypoxic microenvironment found in pancreatic ductal adenocarcinoma and other solid tumors is central to physiological and metabolic alterations of immune cells that significantly impact tumor growth dynamics. Hypoxic adaptations in the immune cells are primarily mediated by the stabilization of hypoxia-inducible factor-1 alpha (HIF-1α), which regulates cellular metabolism by modulating glycolysis and other interconnected metabolic pathways. HIF-1α plays distinct roles in M1 and M2 macrophage polarization, which, in turn, regulates tumor cell immune escape and growth. In this chapter, we describe a real-time PCR-based assay to monitor the transcript levels of Arg1 and Nos2 to assess the status of tumor-induced macrophage polarization under hypoxic conditions. This method can be effectively utilized to delineate the genes critical for M1/M2 polarization in the hypoxic tumor microenvironment and would provide opportunities to develop immunomodulating therapies to regulate the tumor growth, progression, and metastatic dissemination.
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