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Table 1 Spatial heterogeneity of macrophages in the TME

From: Macrophage barrier in the tumor microenvironment and potential clinical applications

Cancer type

Model source

Technology

Spatial distribution

Ref.

Breast cancer

Human

Visium, scRNA-seq

Regions of elevated type I interferon within tumors exhibit an enrichment of CXCL10+ TAMs, which interact with T cells.

[29]

Hepatocellular carcinoma

Human

Visium

The central tumor core shows significant upregulation of CCL15 expression, attracting and polarizing M2-like macrophages.

[30]

Melanoma

Human

DSP, PickSeq, CyCIF

Macrophages with high PDL1 expression infiltrate the invasive tumor border, inhibiting immune cytotoxicity by engaging with PD1+ CTLs.

[31]

Neuroblastoma

AlkF1178L; TH-MYCN or AlkY1282S; TH-MYCN mice

Visium, scRNA-seq, TCR repertoire

Co-localization of CD4+ T cells and macrophages.

[32]

Gliomas

Human

ISH, scRNA-seq, WES

Blood-derived TAMs significantly infiltrate pre-treated gliomas, congregating around blood vessels and necrotic areas.

[33]

Colorectal cancer

Human

Visium, scRNA-seq

Interaction between FAP+ fibroblasts and SPP1+ macrophages occurs in CRC. Their coexistence is linked to extracellular matrix expression.

[18]

Non-small cell lung carcinoma

Mice C57BL/6, Ms4a3-tdTom reporter and CD169-DT; Human

scRNA-seq, scATAC-seq

Tissue-resident macrophages accumulate near tumor cells during the early stages of tumor formation.

[15]