肺癌
NF-κB
癌变
癌症研究
癌症
细胞
NFKB1型
肺
医学
肿瘤进展
生物
免疫学
病理
转录因子
炎症
内科学
基因
遗传学
作者
Fan Sun,Yadong Xiao,Steven D. Shapiro,Zhaoxia Qu,Gutian Xiao
出处
期刊:JCI insight
[American Society for Clinical Investigation]
日期:2024-02-21
卷期号:9 (4)
被引量:1
标识
DOI:10.1172/jci.insight.164188
摘要
Different from the well-studied canonical NF-κB member RelA, the role of the noncanonical NF-κB member NF-κB2 in solid tumors, and lung cancer in particular, is poorly understood. Here we report that in contrast to the tumor-promoting role of RelA, NF-κB2 intrinsic to lung epithelial and tumor cells had no marked effect on lung tumorigenesis and progression. On the other hand, NF-κB2 limited dendritic cell number and activation in the lung but protected lung macrophages and drove them to promote lung cancer through controlling activation of noncanonical and canonical NF-κB, respectively. NF-κB2 was also required for B cell maintenance and T cell activation. The antitumor activity of lymphocyte NF-κB2 was dominated by the protumor function of myeloid NF-κB2; thus, NF-κB2 has an overall tumor-promoting activity. These studies reveal a cell type-dependent role for NF-κB2 in lung cancer and help understand the complexity of NF-κB action and lung cancer pathogenesis for better design of NF-κB-targeted therapy against this deadliest cancer.
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