Abstract

A large-scale single-cell RNA-seq analysis of tumor-associated macrophages in gliomas has unveiled a new aspect of the complex tumor microenvironment and new biomarkers.

Highlights

  • Tumor heterogeneity is determined by both heterogeneous tumor cells and a complex tumor microenvironment

  • The binary ontogeny model versus the continuum model of macrophages Tumor-associated macrophages (TAMs) are abundant in gliomas and evidence suggests that these TAMs

  • The data show a significant increase in blood-derived TAMs, but not in microglial TAMs, in glioblastoma compared to low-grade glioma (Fig. 5a in [8])

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Summary

Introduction

Tumor heterogeneity is determined by both heterogeneous tumor cells and a complex tumor microenvironment. The binary ontogeny model versus the continuum model of macrophages Tumor-associated macrophages (TAMs) are abundant in gliomas and evidence suggests that these TAMs This distinct pattern indicates different underlying mechanisms in low-grade glioma and glioblastoma.

Results
Conclusion
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