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淋巴细胞特异性蛋白 1 表达水平升高参与胶质母细胞瘤中白细胞迁移和免疫抑制微环境的调节。

Elevated lymphocyte specific protein 1 expression is involved in the regulation of leukocyte migration and immunosuppressive microenvironment in glioblastoma.

机构信息

Department of Neurosurgery, The First Hospital of China Medical University, Shenyang, Liaoning 110001, China.

Department of Biochemistry, School of Life Science, China Medical University, Shenyang, Liaoning 110122, China.

出版信息

Aging (Albany NY). 2020 Jan 29;12(2):1656-1684. doi: 10.18632/aging.102706.

DOI:10.18632/aging.102706
PMID:32003759
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7053627/
Abstract

Immune cell infiltration mediates therapeutic response to immune therapies. The investigation on the genes regulating leukocyte migration may help us to understand the mechanisms regulating immune cell infiltration in tumor microenvironment. Here, we collected the data from Chinese Glioma Genome Atlas (CGGA) and The Cancer Genome Atlas (TCGA) to analyze the expression of leukocyte migration related genes in glioblastoma (GBM). Lymphocyte specific protein 1 (LSP1) was identified as the only gene in this family which not only has an elevated expression, but also serve as an independent predictive factor for progressive malignancy in glioma. We further confirmed these results in clinical glioma samples by quantitative PCR, immunofluorescence, immunohistochemistry, and western blot. Moreover, expression was closely related to the response to radio- and chemotherapy in GBM, and positively correlated with immunosuppressive cell populations, including M2 macrophages, neutrophil, and regulatory T cell. Additionally, elevated LSP-1 expression enhanced the expression of immunosuppression related genes like programmed cell death 1 (PD1) and leukocyte associated immunoglobulin like receptor 1 (LAIR1) in macrophages. LSP1 also promoted the migration of macrophages. Together, our study suggests a novel role of LSP1 contributing to immunosuppressive microenvironment in GBM and serving as a potential therapeutic target for it.

摘要

免疫细胞浸润介导免疫治疗的疗效。研究调节白细胞迁移的基因可能有助于我们了解肿瘤微环境中免疫细胞浸润的调控机制。在这里,我们收集了中国脑胶质瘤基因组图谱(CGGA)和癌症基因组图谱(TCGA)的数据,分析了胶质母细胞瘤(GBM)中白细胞迁移相关基因的表达。淋巴细胞特异性蛋白 1(LSP1)是该家族中唯一一种不仅表达上调,而且作为胶质瘤进行性恶性的独立预测因子的基因。我们通过定量 PCR、免疫荧光、免疫组化和 Western blot 进一步在临床胶质瘤样本中证实了这些结果。此外,表达与 GBM 对放化疗的反应密切相关,并与免疫抑制性细胞群呈正相关,包括 M2 巨噬细胞、中性粒细胞和调节性 T 细胞。此外,LSP-1 的高表达增强了巨噬细胞中免疫抑制相关基因如程序性细胞死亡蛋白 1(PD1)和白细胞相关免疫球蛋白样受体 1(LAIR1)的表达。LSP1 还促进了巨噬细胞的迁移。总之,我们的研究表明 LSP1 在 GBM 中具有促进免疫抑制微环境的新作用,并可能成为其潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55a/7053627/5828c137abd3/aging-12-102706-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55a/7053627/1c6e3fe65db8/aging-12-102706-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e55a/7053627/17529b557320/aging-12-102706-g002.jpg
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