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Background <p>Glioblastoma (GBM) remains a lethal brain tumor with limited therapeutic options. Metabolic reprogramming, particularly lactate metabolism, plays a critical role in tumor progression and immune evasion.</p> Methods <p>Here, we integrated single-cell RNA sequencing (scRNA-seq), spatial transcriptomics, and machine learning to investigate the heterogeneity of lactate metabolism in GBM.</p> Results <p>Using scRNA-seq data (GSE138794), we classified neoplastic cells into high- and low-lactate subgroups and identified nuclear factor of activated T-cells cytoplasmic 4 (NFATc4) as a key transcription factor associated with elevated lactate metabolism. Pseudotime trajectory analysis revealed dynamic upregulation of NFATc4 during neoplastic cell differentiation, correlating with invasive phenotypes. Spatial transcriptomics (GSE194329) demonstrated colocalization of NFATc4⁺ tumor cells with SPP1⁺ macrophages, suggesting their microenvironmental crosstalk. A prognostic model constructed via 101 machine-learning algorithms (StepCox[forward] + RSF) achieved favorable performance across independent cohorts (TCGA, CGGA, GSE108474, GSE4412, and meta-cohort). Patients with different risk levels showed distinct immune infiltration, copy number alterations, and drug-sensitivity profiles. In vitro functional assays confirmed that NFATc4 knockdown in GBM cells suppressed tumor cell proliferation, migration, and cell cycle while promoting apoptosis. Besides, NFATc4 knockdown in GBM cells reduced SPP1 expression, migration, and M2-like polarization of co-cultured macrophages. Moreover, silencing SPP1 in macrophages attenuated the pro-tumorigenic effects on co-cultured GBM cells, validating the functional relevance of the NFATc4–SPP1 axis.</p> Conclusion <p>Our study reveals lactate metabolism-related NFATc4 as a promising therapeutic target in GBM, with implications for prognosis stratification and combination therapy.</p>

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Integrative single-cell and spatial transcriptomic analysis reveals a lactate-driven crosstalk between NFATc4⁺ tumor cells and SPP1⁺ macrophages in glioblastoma

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年7月11日

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  • Ruoli Wang,
  • Wantao Wu,
  • Xuan Wu,
  • Ye Yuan,
  • Zhongyi Zhang,
  • Junyi Chen,
  • Yuxin Xie,
  • Linhui Zhang,
  • Xinrui Yu,
  • Hao Zhang,
  • Zongyi Xie

摘要

Background

Glioblastoma (GBM) remains a lethal brain tumor with limited therapeutic options. Metabolic reprogramming, particularly lactate metabolism, plays a critical role in tumor progression and immune evasion.

Methods

Here, we integrated single-cell RNA sequencing (scRNA-seq), spatial transcriptomics, and machine learning to investigate the heterogeneity of lactate metabolism in GBM.

Results

Using scRNA-seq data (GSE138794), we classified neoplastic cells into high- and low-lactate subgroups and identified nuclear factor of activated T-cells cytoplasmic 4 (NFATc4) as a key transcription factor associated with elevated lactate metabolism. Pseudotime trajectory analysis revealed dynamic upregulation of NFATc4 during neoplastic cell differentiation, correlating with invasive phenotypes. Spatial transcriptomics (GSE194329) demonstrated colocalization of NFATc4⁺ tumor cells with SPP1⁺ macrophages, suggesting their microenvironmental crosstalk. A prognostic model constructed via 101 machine-learning algorithms (StepCox[forward] + RSF) achieved favorable performance across independent cohorts (TCGA, CGGA, GSE108474, GSE4412, and meta-cohort). Patients with different risk levels showed distinct immune infiltration, copy number alterations, and drug-sensitivity profiles. In vitro functional assays confirmed that NFATc4 knockdown in GBM cells suppressed tumor cell proliferation, migration, and cell cycle while promoting apoptosis. Besides, NFATc4 knockdown in GBM cells reduced SPP1 expression, migration, and M2-like polarization of co-cultured macrophages. Moreover, silencing SPP1 in macrophages attenuated the pro-tumorigenic effects on co-cultured GBM cells, validating the functional relevance of the NFATc4–SPP1 axis.

Conclusion

Our study reveals lactate metabolism-related NFATc4 as a promising therapeutic target in GBM, with implications for prognosis stratification and combination therapy.