癌症研究
肝细胞癌
生物
肿瘤进展
肿瘤微环境
干细胞
CXCL5型
癌细胞
癌症
内科学
趋化因子
细胞生物学
医学
免疫学
炎症
肿瘤细胞
遗传学
作者
Shao‐Lai Zhou,Dan Yin,Zhiqiang Hu,Chu‐Bin Luo,Zheng‐Jun Zhou,Haoyang Xin,Xin‐Rong Yang,Ying–Hong Shi,Zheng Wang,Xiaowu Huang,Ya Cao,Jia Fan,Jian Zhou
出处
期刊:Hepatology
[Wiley]
日期:2019-04-01
卷期号:70 (4): 1214-1230
被引量:161
摘要
Tumor‐associated neutrophils (TANs) play a crucial role in tumor development and progression in the cancer microenvironment. Despite increased understanding of TAN contributions to hepatocellular carcinoma (HCC) progression and prognosis, the direct interaction between TANs and HCC cells is not fully understood. In this study, we tested the effect of TANs on HCC cells in vitro and in vivo and investigated the mechanism of interaction between them. Our results showed that TANs secreted bone morphogenetic protein 2 and transforming growth factor beta 2 and triggered microRNA 301b‐3p (miR‐301‐3p) expression in HCC cells, subsequently suppressed gene expression of limbic system–associated membrane protein (LSAMP) and CYLD lysine 63 deubiquitinase (CYLD), and increased stem cell characteristics in HCC cells. These TAN‐induced HCC stem‐like cells were hyperactive in nuclear factor kappa B signaling, secreted higher levels of chemokine (C‐X‐C motif) ligand 5 (CXCL5), and recruited more TAN infiltration, suggesting a positive feedback loop. In clinical HCC samples, increased TANs correlated with elevated miR‐301b‐3p, decreased LSAMP and CYLD expression, and increased nuclear p65 accumulation and CXCL5 expression, all of which predicted patient outcome. Conclusion : Our work identified a positive feedback loop governing cancer stem‐like cells and TANs in HCC that controls tumor progression and patient outcome.
科研通智能强力驱动
Strongly Powered by AbleSci AI