From single-cell snapshots to spatial panoramas – a holistic multiomics map of glioblastoma.

Single-cell studies have replaced bulk TCGA "subtypes" with a dynamic model in which multiple malignant programs interconvert in glioblastoma, and the balance among these programs is shaped by genetic lesions and local ecological cues. These programmes mirror distorted developmental gene programmes,...

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Publicado en:Visualized Cancer Medicine Vol. 6; pp. 1 - 11
Autores principales: Yan, Rui, Song, Xiaowei, Hu, Yishan, Wang, Yi, Lv, Yanju, Jiang, Kaiteng, Li, Li, Hu, Yizhou
Formato: pictorial review tables/charts Journal Article
Publicado: EDP Sciences 2025
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 2025
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      pub: EDP Sciences
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        191728812
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        atl: From single-cell snapshots to spatial panoramas – a holistic multiomics map of glioblastoma.
      aug:
        au:
          Yan, Rui
          Song, Xiaowei
          Hu, Yishan
          Wang, Yi
          Lv, Yanju
          Jiang, Kaiteng
          Li, Li
          Hu, Yizhou
        affil: Department of Oncology, the Second Affiliated Hospital of Harbin Medical University, Harbin, 150080, China
      sug:
        subj:
          Glioma Physiopathology
          Multiomics
          Genomics
          Transcriptomes
          Gene Expression Profiling
          Hypoxia, Brain
          Neoplastic Processes
          RNA Analysis
          Sequence Analysis
          Epidermal Growth Factor Receptors
          Cytokines
          Proteomics
          Mass Spectrometry
          Glial Cells
          Macrophages
      ab: Single-cell studies have replaced bulk TCGA "subtypes" with a dynamic model in which multiple malignant programs interconvert in glioblastoma, and the balance among these programs is shaped by genetic lesions and local ecological cues. These programmes mirror distorted developmental gene programmes, and their intrinsic developmental plasticity fuels state switching and therapeutic escape. Spatial multi-omics now anchors these programs to anatomy, revealing a reproducible, hypoxia-graded five-layer architecture from necrotic core to infiltrative rim and identifying hypoxia as a long-range organizer. Whole-tumour 3D sampling links clonal evolution to territory, showing that early driver events can span the lesion, while later changes remain regionally restricted. This geography-aware view helps explain why single agents often fail and points to niche-targeted combinations and delivery strategies tailored to the blood-tumour barrier states. We outline how an integrated, spatially resolved multi-omics atlas can guide compartment-specific therapy and prospective monitoring in precision neuro-oncology.
      pubtype: Academic Journal
      doctype:
        pictorial
        review
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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