Novel tumor-associated macrophage populations and subpopulations by single cell RNA sequencing

Juanjuan Wang1,2,3, Ningning Zhu1,2,3, Xiaomin Su1,2,3

  • 1Translational Medicine Institute, Affiliated Tianjin Union Medical Center of Nankai University, Nankai University, Tianjin, China.

Frontiers in Immunology
|February 13, 2024
PubMed

Insights

Tumor-associated macrophages (TAMs) exhibit distinct subtypes, including FCN1+, SPP1+, C1Q+, and CCL18+ TAMs. These subpopulations play crucial roles in tumor progression, immune suppression, and metastasis.

Area of Science:

  • Oncology
  • Immunology
  • Genomics

Background:

  • Tumor-associated macrophages (TAMs) are prevalent in solid tumors.
  • TAMs influence immune regulation, angiogenesis, metastasis, and therapy resistance.
  • The precise functions of TAM subpopulations remain largely undefined.

Purpose of the Study:

  • To review novel TAM subpopulations identified by single-cell RNA sequencing (scRNA-seq).
  • To elucidate the distinct functions of FCN1+, SPP1+, C1Q+, and CCL18+ TAMs in solid tumors.

Main Methods:

  • Analysis of scRNA-seq data from various solid tumor tissues.
  • Identification of TAM subpopulations based on core gene signatures.
  • Functional enrichment and gene expression analysis.

Main Results:

  • FCN1+ TAMs are associated with inflammation.
  • SPP1+ TAMs may drive metastasis, angiogenesis, and cancer stem cell activation.
  • C1Q+ TAMs are implicated in immune regulation and suppression.
  • CCL18+ TAMs exhibit potent immunosuppression and enhance metastasis.
  • SPP1+ and C1Q+ TAMs can be further subdivided into functionally distinct populations.

Conclusions:

  • scRNA-seq reveals distinct TAM subpopulations with specialized functions in solid tumors.
  • Understanding these subpopulations is crucial for targeted cancer therapies.
  • Further research is needed to bridge the gap between identified subpopulations and their precise functional roles.