CCR2型
转移
微生物群
四氯化碳
单核细胞
免疫系统
癌症研究
趋化因子
免疫学
下调和上调
医学
生物
内科学
趋化因子受体
生物信息学
癌症
基因
生物化学
作者
Wenzhong Zhang,Jie Ling,Baiying Xu,Jie Wang,Zexu Chen,Gang Li
标识
DOI:10.1016/j.intimp.2024.111877
摘要
The gut microbiome plays an important role in tumor growth by regulating immune cell function. However, the role of the gut microbiome-mediated monocytes in liver metastasis remains unclear. In this study, we found that fecal microbiome transplantation (FMT) from the stool of patients with liver metastasis (LM) significantly promoted liver metastasis compared with healthy donors (HD). Monocytes were upregulated in liver tissues by the CCL2/CCR2 axis in LM patients' stool transplanted mouse model. CCL2/CCR2 inhibition and monocyte depletion significantly suppress liver metastasis. FMT using LM patients' stool enhanced the plasma lipopolysaccharides (LPS) concentration. The LPS/TLR4 signaling pathway is crucial for gut microbiome-mediated liver metastasis. These results indicated that monocytes contribute to liver metastasis via the CCL2/CCR2 axis.
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