CLEC7A regulates M2 macrophages to suppress the immune microenvironment and implies poorer prognosis of glioma

CLEC7A 调节 M2 巨噬细胞以抑制免疫微环境并暗示胶质瘤预后较差

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作者:Jinchao Wang #, Xiaoru Li #, Kai Wang, Kaiji Li, Yalong Gao, Jianye Xu, Ruilong Peng, Xu Zhang, Shu Zhang, Yuan Zhou, Shangchen Xu, Jianning Zhang

Background

Gliomas constitute a category of malignant tumors originating from brain tissue, representing the majority of intracranial malignancies. Previous research has demonstrated the pivotal role of CLEC7A in the progression of various cancers, yet its specific implications within gliomas remain elusive. The primary

Conclusion

CLEC7A expression is intricately linked to the pathology and molecular characteristics of gliomas, establishing its role as an independent prognostic factor for gliomas and influencing macrophage function. It could be a promising target for immunotherapy in gliomas.

Methods

This investigation involved examining and validating the relationship between CLEC7A and glioma using samples from Hospital, along with data from TCGA, GEO, GTEx, and CGGA datasets. Subsequently, we explored its prognostic value, biological functions, expression location, and impact on immune cells within gliomas. Finally, we investigated its potential impact on the chemotaxis and polarization of macrophages.

Results

The expression of CLEC7A is upregulated in gliomas, and its levels escalate with the malignancy of tumors, establishing it as an independent prognostic factor. Functional enrichment analysis revealed a significant correlation between CLEC7A and immune function. Subsequent examination of immune cell differential expression demonstrated a robust association between CLEC7A and M2 macrophages. This

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