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Updated: Jul 13, 2026

Studying the Effects of Tumor-Secreted Paracrine Ligands on Macrophage Activation using Co-Culture with Permeable Membrane Supports
Published on: November 28, 2019
Metabolic mechanisms of cancer-induced inhibition of immune responses
Antonella Viola1, Vincenzo Bronte
1Venetian Institute of Molecular Medicine, Padua, Italy; Istituto Clinico Humanitas IRCCS, Via Manzoni 56, 20089 Rozzano, Milan, Italy. antonella.viola@unipd.it
Abstract:
During progression, tumors become refractory to the offensive weapons of the immune system. It has been known for a long time that the tumor microenvironment presents a profound modification in the metabolism of arachidonic acid and amino acids such as l-triptophan and l-arginine. However, only in the last decade we have started to appreciate how these changes might cause dysfunctions in cells of both adaptive and innate immune system. The knowledge of these complex and partially interconnected metabolic pathways is offering new targets for an integrated pharmacological approach aiming at freeing tumor-specific T lymphocytes from the latches of cancer influence.
Insights
Tumors evade immune attack by altering metabolism of key nutrients like arachidonic acid and amino acids. Understanding these metabolic changes offers new therapeutic targets to restore anti-cancer immune responses.
Area of Science:
- Immunology
- Cancer Biology
- Metabolic Pathways
Background:
- Tumor progression often leads to immune evasion.
- The tumor microenvironment significantly alters host metabolism.
- Dysregulation of arachidonic acid and amino acid metabolism impacts immune cells.
Purpose of the Study:
- To investigate how tumor microenvironment-induced metabolic changes affect immune cells.
- To identify novel therapeutic targets for overcoming cancer-induced immune suppression.
Main Methods:
- Analysis of metabolic alterations in the tumor microenvironment.
- Assessment of immune cell function in relation to metabolic changes.
- Exploration of pharmacological interventions targeting metabolic pathways.
Main Results:
- Tumor progression is associated with significant metabolic reprogramming.
- Altered metabolism of arachidonic acid and amino acids (l-tryptophan, l-arginine) impairs immune cell function.
- These metabolic changes contribute to immune evasion by cancer.
Conclusions:
- Metabolic pathways in the tumor microenvironment are critical regulators of anti-tumor immunity.
- Targeting these metabolic vulnerabilities presents a promising strategy for cancer immunotherapy.
- Restoring immune cell function through metabolic intervention can enhance anti-cancer T cell responses.
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