Abstract 7746: CEACAM5/6+ cancer cell and IL1B+ macrophage-mediated resistance in anti-PD-1 treated gastric cancer

Abstract Immune checkpoint blockade therapy has shown limited efficacy in gastric cancer, with most patients developing resistance through mechanisms that remain incompletely defined. Here, we generate a comprehensive single-cell RNA sequencing atlas of 526,583 cells from gastric cancer patients treated with anti-PD-1 plus chemotherapy, analyzing paired pre- and post-treatment samples to capture dynamic resistance mechanisms. We identify two distinct resistance pathways that emerge during treatment. First, CEACAM5/6+ cancer cells are markedly enriched in pre-treatment non-responders and predict treatment failure. These CEACAM5/6+ epithelial cells show the highest tumor scores and correlate with increased regulatory T cell infiltration expressing CEACAM1, establishing an alternative checkpoint axis that bypasses PD-1/PD-L1 blockade. External validation in independent cohorts confirms CEACAM5/6 expression as a robust predictor of anti-PD-1 resistance. Second, we uncover a macrophage-driven inflammatory cascade central to treatment resistance. IL-1β+ macrophages serve as the primary source of NF-κB pathway activation across the tumor microenvironment, triggering downstream IL-6 production, Th17 cell differentiation, chronic inflammation and epithelial-mesenchymal transition. This macrophage module is significantly enriched in post-treatment non-responders, with TNF-high expressing monocyte-macrophages absent in responders but prevalent in resistant tumors. The resulting inflammatory milieu drives PD-L1 upregulation across multiple cell types, creating a self-reinforcing immunosuppressive niche. Collectively, these findings nominate CEACAM5/6+ epithelial cells and IL-1β+ inflammatory macrophages as actionable therapeutic targets for overcoming anti-PD-1 resistance in gastric cancer, providing a mechanistic framework and rational blueprint for next-generation combination immunotherapy strategies. Citation Format: Liudeng Zhang, Jian Chen, Yikai Luo, Lie Wang, Han Liang. CEACAM5/6+ cancer cell and IL1B+ macrophage-mediated resistance in anti-PD-1 treated gastric cancer [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 7746.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-7746
Primary Topic
Cancer Immunotherapy and Biomarkers
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article
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article

Abstract 7746: CEACAM5/6+ cancer cell and IL1B+ macrophage-mediated resistance in anti-PD-1 treated gastric cancer

Han Liang, Lie Wang, Yikai Luo, Liudeng Zhang et al.
Cancer Research
Cancer Immunotherapy and Biomarkers
article

Abstract 7746: CEACAM5/6+ cancer cell and IL1B+ macrophage-mediated resistance in anti-PD-1 treated gastric cancer

Han Liang, Lie Wang, Yikai Luo, Liudeng Zhang, Jian Chen
article en

Abstract

Abstract Immune checkpoint blockade therapy has shown limited efficacy in gastric cancer, with most patients developing resistance through mechanisms that remain incompletely defined. Here, we generate a comprehensive single-cell RNA sequencing atlas of 526,583 cells from gastric cancer patients treated with anti-PD-1 plus chemotherapy, analyzing paired pre- and post-treatment samples to capture dynamic resistance mechanisms. We identify two distinct resistance pathways that emerge during treatment. First, CEACAM5/6+ cancer cells are markedly enriched in pre-treatment non-responders and predict treatment failure. These CEACAM5/6+ epithelial cells show the highest tumor scores and correlate with increased regulatory T cell infiltration expressing CEACAM1, establishing an alternative checkpoint axis that bypasses PD-1/PD-L1 blockade. External validation in independent cohorts confirms CEACAM5/6 expression as a robust predictor of anti-PD-1 resistance. Second, we uncover a macrophage-driven inflammatory cascade central to treatment resistance. IL-1β+ macrophages serve as the primary source of NF-κB pathway activation across the tumor microenvironment, triggering downstream IL-6 production, Th17 cell differentiation, chronic inflammation and epithelial-mesenchymal transition. This macrophage module is significantly enriched in post-treatment non-responders, with TNF-high expressing monocyte-macrophages absent in responders but prevalent in resistant tumors. The resulting inflammatory milieu drives PD-L1 upregulation across multiple cell types, creating a self-reinforcing immunosuppressive niche. Collectively, these findings nominate CEACAM5/6+ epithelial cells and IL-1β+ inflammatory macrophages as actionable therapeutic targets for overcoming anti-PD-1 resistance in gastric cancer, providing a mechanistic framework and rational blueprint for next-generation combination immunotherapy strategies. Citation Format: Liudeng Zhang, Jian Chen, Yikai Luo, Lie Wang, Han Liang. CEACAM5/6+ cancer cell and IL1B+ macrophage-mediated resistance in anti-PD-1 treated gastric cancer [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 7746.

Cancer ResearchVol. 86(7_Supplement)
The University of Texas MD Anderson Cancer Center (US), Zhejiang University (CN)
Good health and well-being
Openalex Percentile: Top 9%
Cancer Immunotherapy and Biomarkers
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