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Background <p>Stem-like gastric cancer (GC) is an aggressive molecular subtype marked by poor prognosis and limited response to immune checkpoint blockade (ICB). The spatial mechanisms driving this resistance remain unclear.</p> Methods <p>We conducted spatially resolved single-cell transcriptomic profiling of diffuse-type GC tissues to uncover the spatial architecture and functional diversity of tumor and stromal populations. Cellular heterogeneity and region-specific signaling pathways were characterized using integrative bioinformatics analyses.</p> Results <p>We identified transcriptionally diverse, high-entropy cell populations predominantly localized in the deep tumor regions. These included unique endothelial and fibroblast subsets enriched for pro-tumorigenic and immune-regulatory signaling. A notable finding was the engagement of deep-region endothelial cells in <i>VISFATIN</i> (extracellular <i>NAMPT</i>) signaling through the<i> ITGA5–ITGB1</i> integrin axis, associated with immune evasion and poor prognosis. This endothelial signaling program is distinct from and functionally independent of cancer-associated fibroblast (CAF)-mediated pathways. Elevated expression of the <i>NAMPT–ITGA5–ITGB1</i> axis was observed in ICB non-responders and correlated with reduced overall survival.</p> Conclusions <p>Our study delineates spatially defined cellular programs that contribute to immune escape in stem-like GC, highlighting a novel VISFATIN–integrin signaling axis as a potential biomarker and therapeutic target in immunotherapy-resistant tumors.</p>

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Spatially resolved endothelial signaling via nampt-itga5 drives immune evasion in stem-like gastric cancer

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年9月29日

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  • Ji-Yong Sung,
  • Jae-Ho Cheong,
  • Eui Tae Kim

摘要

Background

Stem-like gastric cancer (GC) is an aggressive molecular subtype marked by poor prognosis and limited response to immune checkpoint blockade (ICB). The spatial mechanisms driving this resistance remain unclear.

Methods

We conducted spatially resolved single-cell transcriptomic profiling of diffuse-type GC tissues to uncover the spatial architecture and functional diversity of tumor and stromal populations. Cellular heterogeneity and region-specific signaling pathways were characterized using integrative bioinformatics analyses.

Results

We identified transcriptionally diverse, high-entropy cell populations predominantly localized in the deep tumor regions. These included unique endothelial and fibroblast subsets enriched for pro-tumorigenic and immune-regulatory signaling. A notable finding was the engagement of deep-region endothelial cells in VISFATIN (extracellular NAMPT) signaling through the ITGA5–ITGB1 integrin axis, associated with immune evasion and poor prognosis. This endothelial signaling program is distinct from and functionally independent of cancer-associated fibroblast (CAF)-mediated pathways. Elevated expression of the NAMPT–ITGA5–ITGB1 axis was observed in ICB non-responders and correlated with reduced overall survival.

Conclusions

Our study delineates spatially defined cellular programs that contribute to immune escape in stem-like GC, highlighting a novel VISFATIN–integrin signaling axis as a potential biomarker and therapeutic target in immunotherapy-resistant tumors.