PI3K/AKT/mTOR通路
癌症研究
免疫系统
PD-L1
生物
细胞生物学
信号转导
免疫学
免疫疗法
作者
Pei Zhang,Shuwen Yu,Hongyu Li,Chuanyong Liu,Juan Li,Wenli Lin,Aiqin Gao,Linlin Wang,Wei Gao,Yuping Sun
出处
期刊:FEBS Letters
[Wiley]
日期:2015-07-03
卷期号:589 (17): 2248-2256
被引量:82
标识
DOI:10.1016/j.febslet.2015.06.037
摘要
Immunoglobulin-like transcript (ILT) 4 is critical for the inhibitory function of certain immune cells. We previously demonstrated that ILT4 is over-expressed in human non-small cell lung cancer (NSCLC) cells and is involved in tumour evasion via an unknown mechanism. In this report, we demonstrate that ILT4 increases the expression of the co-inhibitory molecule B7-H3 through PI3K/AKT/mTOR signalling. In primary human NSCLC tissues, a significant positive relationship is observed between ILT4 and B7-H3 expression. ILT4/B7-H3 co-expression is significantly associated with a reduction in T infiltrating lymphoid cells and lower overall survival. In summary, ILT4 increases B7-H3 expression and ILT4/B7-H3 co-expression may be involved in NSCLC progression.
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