# Immunometabolic editing of the tumor microenvironment: from reprogramming mechanisms to therapeutic vulnerabilities

**Authors:** Yixin Li, Yunmei Zhang, Yan Nie, Xueman Chen

PMC · DOI: 10.3389/fimmu.2025.1678446 · 2026-01-16

## TL;DR

This review explores how metabolic changes in the tumor environment shape immune responses and how targeting these changes could improve cancer immunotherapies.

## Contribution

The paper introduces the concept of immunometabolic editing as a dynamic process shaping anti-tumor immunity and identifies therapeutic targets.

## Key findings

- Metabolic reprogramming in the tumor microenvironment influences immune cell function and tumor-immune interactions.
- Immunometabolic editing is a co-evolutionary process that affects anti-tumor immune responses and immune evasion.
- Targeted immunometabolic interventions may enhance anti-tumor immunity and improve immunotherapy outcomes.

## Abstract

Metabolic reprogramming is not only one of the malignant characteristics of tumor cells, but also commonly seen in a variety of immune cells in tumor microenvironment(TME), which massively promotes tumor-body immune interaction. Immunometabolic editing is a dynamic, co-evolutionary process wherein adaptive metabolic reprogramming in the TME, driven by tumor-immune crosstalk during immunoediting, critically shapes anti-tumor immune response and governs immune evasion. Studies of metabolic pathways linked to anti-tumor immune process and discoveries of important therapeutic targets are conducive to the development of targeted immunometabolic intervention to enhance the body’s anti-tumor immune response and improve the efficacy of tumor immunotherapies. This review summarizes metabolic characteristics of the TME, highlights immunometabolic editing during cancer evolution, and discusses mechanisms by which tumor immunotherapies modulate tumor immunometabolism to identify potential therapeutic targets.

## Full-text entities

- **Diseases:** cancer (MESH:D009369)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12855416/full.md

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Source: https://tomesphere.com/paper/PMC12855416