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] |