What question did this study set out to answer?

To investigate how tumor-intrinsic IRE1α signaling affects immune evasion and resistance to immune checkpoint inhibitors in NSCLC.

April 5, 2026

Abstract 2916: Tumor-intrinsic IRE1α signaling drives immune evasion and resistance to immune checkpoint inhibitor in lung cancer by upregulating PD-L1 and remodeling the tumor microenvironment

Puntos clave

To investigate how tumor-intrinsic IRE1α signaling affects immune evasion and resistance to immune checkpoint inhibitors in NSCLC.
Correlated IRE1α activity with prognosis and resistance to immune checkpoint inhibitors in NSCLC patients.
Analyzed the effects of IRE1α activation on the tumor microenvironment using patient samples.
Used genetic ablation of IRE1α in immunocompetent mice to study tumor growth and immune cell infiltration.
Examined the role of CCL20 in macrophage differentiation and tumor progression in vitro.
Investigation of the mechanistic pathways involving PD-L1 expression and chemokine production.
High IRE1α activity is linked to poor patient prognosis and treatment resistance.
IRE1α activation is associated with an immunosuppressive tumor microenvironment enriched in regulatory T-cells and M2-like macrophages.
Genetic loss of IRE1α reduced tumor growth and increased CD8+ T-cell presence in mice.
IRE1α promoted secretion of CCL20, enhancing M2-like macrophage differentiation.
IRE1α-XBP1s signaling directly upregulated PD-L1 via specific signaling pathways.

Resumen

Abstract Tumor cells exploit endoplasmic reticulum (ER) stress pathways for survival. While the role of the unfolded protein response in tumorigenesis is well-established, its specific effect on the tumor microenvironment (TME) and therapeutic resistance in non-small cell lung cancer (NSCLC), particularly via IRE1α signaling, remains poorly understood. Here, we demonstrate that high IRE1α activity correlates with poor prognosis and resistance to immune checkpoint inhibitors in NSCLC patients. IRE1α activation was associated with an immunosuppressive TME, characterized by enriched regulatory T-cell (Treg) and M2-like tumor-associated macrophage (TAM) signatures in patient cohorts. Consistently, genetic ablation of tumor-intrinsic IRE1α (ERN1 KO) in immunocompetent mice significantly attenuated tumor growth and enhanced CD8+ T-cell infiltration. Mechanistically, IRE1α promoted the expression and secretion of key chemokines, specifically CCL20, which in turn drove M2-like macrophage differentiation in vitro. Notably, this pro-tumorigenic secretome was abrogated by the IRE1α inhibitor MKC8866. Concurrently, IRE1α-XBP1s signaling synergized with IFNγ to directly upregulate tumor-intrinsic PD-L1 expression. This process was mediated by the activation of the RIG-I-IRF1 axis, sustained STAT1 phosphorylation, and direct XBP1s binding to the CD274 promoter. Collectively, tumor-intrinsic IRE1α orchestrates immune evasion in NSCLC by amplifying tumor-intrinsic PD-L1 expression through the IFNγ-STAT1-XBP1s-IRF1 axis and remodeling the TME via chemokines such as CCL20 that recruit immunosuppressive cell populations. The combination of an IRE1α inhibitor and anti-PD-1 antibody represents a promising strategy to enhance the efficacy of immunotherapy for NSCLC. Citation Format: Youngjoo Jeon, Hyun Kyung Ahn, Hongsoon Kim, Sung-Yup Cho, Jaemoon Koh, Yoon Kyung Jeon. Tumor-intrinsic IRE1α signaling drives immune evasion and resistance to immune checkpoint inhibitor in lung cancer by upregulating PD-L1 and remodeling the tumor microenvironment abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 2916.

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Cite This Study

Jeon et al. (Fri,) studied this question.

synapsesocial.com/papers/69d1fd73a79560c99a0a38f5 https://doi.org/https://doi.org/10.1158/1538-7445.am2026-2916

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