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Hypoxia induced HMGB1 and mitochondrial DNA interactions mediate tumor growth in hepatocellular carcinoma through Toll Like Receptor 9

机译:低氧诱导的HMGB1和线粒体DNA相互作用通过Toll样受体9介导肝细胞癌的肿瘤生长

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摘要

Background and aimsThe mechanisms of hypoxia-induced tumor growth remain unclear. Hypoxia induces intracellular translocation and release of a variety of damage associated molecular patterns (DAMPs) such as nuclear HMGB1 and mitochondrial DNA (mtDNA). In inflammation, Toll-like receptor (TLR)-9 activation by DNA-containing immune complexes has been shown to be mediated by HMGB1. We thus hypothesize that HMGB1 binds mtDNA in the cytoplasm of hypoxic tumor cells and promotes tumor growth through activating TLR9 signaling pathways.
机译:背景与目的缺氧诱导肿瘤生长的机制尚不清楚。缺氧诱导细胞内移位和释放多种损伤相关分子模式(DAMP),例如核HMGB1和线粒体DNA(mtDNA)。在炎症中,HMGB1介导了含DNA的免疫复合物激活Toll样受体(TLR)-9。因此,我们假设HMGB1在缺氧肿瘤细胞的细胞质中结合mtDNA,并通过激活TLR9信号通路促进肿瘤生长。

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