生物
重编程
转移
HMGB1
癌症研究
缺氧(环境)
缺氧诱导因子
渗透(HVAC)
肝细胞癌
巨噬细胞
肿瘤进展
肿瘤相关巨噬细胞
免疫学
肿瘤微环境
细胞
炎症
癌症
肿瘤细胞
体外
化学
基因
氧气
有机化学
物理
热力学
生物化学
遗传学
作者
Jiang Jiang,Guangzhi Wang,Ying Wang,Haozhe Huang,Wentao Li,Xudong Qu
标识
DOI:10.1016/j.yexcr.2018.03.025
摘要
Hypoxia is associated with the progression of hepatocellular carcinoma through promotion of spontaneous metastasis but the mechanism remains unclear. Here, we hypothesis that tumor cell-derived HMGB1 orchestrates macrophages infiltration and promotes metastasis of HCC via enhancing macrophage-secreted IL-6 under hypoxia. HMGB1 expression was robustly exacerbated in tumors of HCC patients with PVTT. Meanwhile, hypoxia exposure gave rise to HMGB1 expression in hepatoma cells of human and mouse in a HIF-1α-dependent manner and subsequently induced the infiltration and reprogramming of macrophages to augment the expression of Il-6. Further study demonstrated macrophage-derived IL-6 enhanced the invasiveness and metastasis of murine HCC cells. Therefore, our study provides a novel understanding of the relationship between tumor cells and tumor associated macrophages (TAMs) in the context of hypoxia.
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