Regulatory and Physiological Roles of lncRNAs in Tumor Immunotherapy Response

Immunotherapy harnesses the patient's immune system to recognize and eliminate malignant cells and constitutes the forefront of cancer therapies. Notwithstanding, intrinsic and acquired immunotherapy resistance mechanisms operating within the tumor microenvironment remain a limitation to achieving durable and effective clinical responses. Long noncoding RNAs (lncRNAs) emerge as critical regulators of gene expression both in tumor and immune cells, modulating processes that affect resistance to immunotherapy response, including T-cell differentiation, macrophage polarization, dendritic cell maturation, and cytokine signaling. Their tissue-specific expression and regulatory roles in the physiology of the tumor immune microenvironment and response to immune checkpoint inhibitors make them attractive molecules to search for predictive biomarkers and targets for combined RNA-based interventions that improve immunotherapy response.

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Publication Details

Journal
Physiology
Published
2026-04-06
DOI
https://doi.org/10.1152/physiol.00058.2025
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
0.00

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article

Regulatory and Physiological Roles of lncRNAs in Tumor Immunotherapy Response

Eduardo M. Reis, Miriam Galvonas Jasiulionis
Physiology
Cancer-related molecular mechanisms research
article

Regulatory and Physiological Roles of lncRNAs in Tumor Immunotherapy Response

Eduardo M. Reis, Miriam Galvonas Jasiulionis
article en

Abstract

Immunotherapy harnesses the patient's immune system to recognize and eliminate malignant cells and constitutes the forefront of cancer therapies. Notwithstanding, intrinsic and acquired immunotherapy resistance mechanisms operating within the tumor microenvironment remain a limitation to achieving durable and effective clinical responses. Long noncoding RNAs (lncRNAs) emerge as critical regulators of gene expression both in tumor and immune cells, modulating processes that affect resistance to immunotherapy response, including T-cell differentiation, macrophage polarization, dendritic cell maturation, and cytokine signaling. Their tissue-specific expression and regulatory roles in the physiology of the tumor immune microenvironment and response to immune checkpoint inhibitors make them attractive molecules to search for predictive biomarkers and targets for combined RNA-based interventions that improve immunotherapy response.

Physiology
Hospital Universitário da Universidade de São Paulo (BR), Universidade Federal de São Paulo (BR)
Fundação de Amparo à Pesquisa do Estado de São Paulo, Conselho Nacional de Desenvolvimento Científico e Tecnológico
Openalex Percentile: Top 25%
Cancer-related molecular mechanisms research
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