巨噬细胞移动抑制因子
SNP公司
免疫系统
癌症研究
生殖系
生物
单核苷酸多态性
胶质母细胞瘤
种系突变
肿瘤微环境
体细胞
细胞因子
免疫学
基因型
基因
遗传学
突变
作者
Tyler J. Alban,Matthew M. Grabowski,Balint Otvos,Defne Bayık,Wesley Wang,Ajay Zalavadia,Vlad Makarov,Katie Troike,Mary McGraw,Anja Rabljenovic,Adam Lauko,Chase Neumann,Gustavo Roversi,Kristin Waite,Gino Cioffi,Nirav Patil,Thuy Tran,Kathleen McCortney,Alicia Steffens,Claudia Marcela Diaz
出处
期刊:JCI insight
[American Society for Clinical Investigation]
日期:2023-05-30
卷期号:8 (13)
被引量:2
标识
DOI:10.1172/jci.insight.160024
摘要
Intratumoral heterogeneity is a defining hallmark of glioblastoma, driving drug resistance and ultimately recurrence. Many somatic drivers of microenvironmental change have been shown to affect this heterogeneity and, ultimately, the treatment response. However, little is known about how germline mutations affect the tumoral microenvironment. Here, we find that the single-nucleotide polymorphism (SNP) rs755622 in the promoter of the cytokine macrophage migration inhibitory factor (MIF) is associated with increased leukocyte infiltration in glioblastoma. Furthermore, we identified an association between rs755622 and lactotransferrin expression, which could also be used as a biomarker for immune-infiltrated tumors. These findings demonstrate that a germline SNP in the promoter region of MIF may affect the immune microenvironment and further reveal a link between lactotransferrin and immune activation.
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