肝细胞癌
小RNA
利基
癌症研究
肺
转移
肺癌
医学
生物
病理
癌症
内科学
基因
遗传学
生物化学
作者
Yingying Zhao,Hongmei Yu,Jiajun Li,Jiali Qian,Miao Li,Xi Zhang,Mimi Wang,Yaohui Wang,Yinying Dong,You Yang,Qiwen Zhou,Dongmei Gao,Yan Zhao,Binbin Liu,Rongxin Chen,Zhenggang Ren,Zhiming Wang,K. Zhang,Jiefeng Cui
标识
DOI:10.1038/s41467-025-56878-8
摘要
Apart from the classic features, it is almost unknown whether there exist other new pathological features during pre-metastatic niche formation in hepatocellular carcinoma (HCC). Our previous works have highlighted the contribution of increased matrix stiffness to lung pre-metastatic niche formation and metastasis in HCC. However, whether increased matrix stiffness influences glucose metabolism and supply of lung pre-metastatic niche remains largely unclear. Here we uncover the underlying mechanism by which matrix stiffness-tuned exosomal miRNAs as the major contributor modulate glucose enrichment during lung pre-metastatic niche formation through decreasing the glucose uptake and consumption of lung fibroblasts and increasing angiogenesis and vascular permeability. Our findings suggest that glucose enrichment, a new characteristic of the lung pre-metastatic niche triggered by matrix stiffness-tuned exosomal miRNAs, is essential for the colonization and survival of metastatic tumor cells, as well as subsequent metastatic foci growth.
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