Editorial: Multi-omics interrogation of tumor-associated macrophages: paving the way for next-generation cancer immunotherapies - Summary - MDSpire
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Editorial: Exploring Multi-Omics Approaches to Tumor-Associated Macrophages: A Pathway to Advanced Cancer Immunotherapy

  • By

  • Shengshan Xu

  • Ke-Jie He

  • Lin Zhang

  • Qian Guo

  • August 25, 2026

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Objective:

To examine tumor-associated macrophages (TAMs) through multi-omics approaches in the context of cancer immunotherapies.

Approach:
  • Research Topic Overview: The Research Topic includes 15 articles that explore TAM biology, focusing on TAM-tumor interactions, immune evasion pathways, and prognostic signatures.
  • TAM Functionality Across Malignancies: Studies analyze TAM functions in various cancers, including breast, ovarian, prostate, lung, gastric, and brain cancers, highlighting their roles in tumor progression and therapeutic resistance.
  • Prognostic Modeling: Machine-learning techniques are employed to create prognostic models based on TAM data, linking TAM characteristics to clinical outcomes.
  • Target Identification: Research identifies novel molecular targets and environmental triggers influencing TAM activation and immune exclusion.
Key Findings:
  • TAMs exhibit significant heterogeneity and plasticity, challenging the traditional M1/M2 classification.
  • Specific TAM subpopulations are linked to immune evasion and resistance to therapies in various cancers.
  • New biomarkers and therapeutic targets such as GPR35, EFNA3, and TIMP1 have been identified for potential clinical application.
Limitations:
  • The complexity of the tumor microenvironment may limit the generalizability of findings across different cancer types.
  • The reliance on multi-omics data requires careful integration and interpretation to avoid misrepresentation of TAM roles.

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