Abstract 6676: Spatial proteomics and AI-driven analysis uncover therapeutic landscapes within the glioblastoma microenvironment

Abstract Glioblastoma (GBM) is a highly aggressive and spatially heterogeneous brain tumor with limited treatment options and poor prognosis. Effective therapeutic targeting requires a deeper understanding of the tumor microenvironment (TME), particularly the spatial relationships between malignant, immune, and stromal compartments. To address this, we employed the Cell DIVE™ multiplex immunofluorescence platform to perform high-plex spatial proteomic profiling of FFPE glioblastoma tissue section. A customized panel of directly conjugated recombinant antibodies from Abcam was optimized to interrogate markers relevant to tumor biology, immune modulation, and stromal architecture. Following iterative staining and imaging cycles, multi-channel, high-resolution images were analyzed using Aivia, an AI-powered image analysis platform. The workflow enabled accurate segmentation of tissue regions and quantification of spatial protein expression patterns across distinct anatomical zones within GBM. Spatial relationships among protein expression patterns revealed region-specific immune infiltration and phenotypic transitions at tumor-stromal interfaces. Co-localization and proximity analysis further identified potential immune evasion signatures and microenvironmental structures associated with resistance phenotypes. This integrative approach provides a scalable and clinically compatible method for spatially resolved proteomic analysis of complex tumor tissues. The combination of Cell DIVE™ multiplex imaging, Abcam direct-conjugate antibodies, and Aivia-based analysis offers a powerful platform for dissecting the spatial biology of glioblastoma. The translational relevance of this study lies in its potential to inform biomarker development, guide spatially targeted therapies, and support precision medicine strategies in GBM. This methodology is well positioned for integration into clinical research workflows and large-scale translational studies, with potential to inform personalized treatment strategies across neuro-oncology and other solid tumors. Citation Format: Nadine Nelson, Hoyin Lai, Sophie Struble, Richard A. Heil-Chapdelaine, Natasha F. Diaz Granados, Arindam Bose. Spatial proteomics and AI-driven analysis uncover therapeutic landscapes within the glioblastoma 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 6676.

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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-6676
Primary Topic
Single-cell and spatial transcriptomics
Type
article
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article

Abstract 6676: Spatial proteomics and AI-driven analysis uncover therapeutic landscapes within the glioblastoma microenvironment

Hoyin Lai, Sophie Struble, Natasha F. Diaz Granados, Nadine Nelson et al.
Cancer Research
Single-cell and spatial transcriptomics
article

Abstract 6676: Spatial proteomics and AI-driven analysis uncover therapeutic landscapes within the glioblastoma microenvironment

Hoyin Lai, Sophie Struble, Natasha F. Diaz Granados, Nadine Nelson, Arindam Bose, Richard A. Heil-Chapdelaine
article en

Abstract

Abstract Glioblastoma (GBM) is a highly aggressive and spatially heterogeneous brain tumor with limited treatment options and poor prognosis. Effective therapeutic targeting requires a deeper understanding of the tumor microenvironment (TME), particularly the spatial relationships between malignant, immune, and stromal compartments. To address this, we employed the Cell DIVE™ multiplex immunofluorescence platform to perform high-plex spatial proteomic profiling of FFPE glioblastoma tissue section. A customized panel of directly conjugated recombinant antibodies from Abcam was optimized to interrogate markers relevant to tumor biology, immune modulation, and stromal architecture. Following iterative staining and imaging cycles, multi-channel, high-resolution images were analyzed using Aivia, an AI-powered image analysis platform. The workflow enabled accurate segmentation of tissue regions and quantification of spatial protein expression patterns across distinct anatomical zones within GBM. Spatial relationships among protein expression patterns revealed region-specific immune infiltration and phenotypic transitions at tumor-stromal interfaces. Co-localization and proximity analysis further identified potential immune evasion signatures and microenvironmental structures associated with resistance phenotypes. This integrative approach provides a scalable and clinically compatible method for spatially resolved proteomic analysis of complex tumor tissues. The combination of Cell DIVE™ multiplex imaging, Abcam direct-conjugate antibodies, and Aivia-based analysis offers a powerful platform for dissecting the spatial biology of glioblastoma. The translational relevance of this study lies in its potential to inform biomarker development, guide spatially targeted therapies, and support precision medicine strategies in GBM. This methodology is well positioned for integration into clinical research workflows and large-scale translational studies, with potential to inform personalized treatment strategies across neuro-oncology and other solid tumors. Citation Format: Nadine Nelson, Hoyin Lai, Sophie Struble, Richard A. Heil-Chapdelaine, Natasha F. Diaz Granados, Arindam Bose. Spatial proteomics and AI-driven analysis uncover therapeutic landscapes within the glioblastoma 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 6676.

Cancer ResearchVol. 86(7_Supplement)
Oracle (United States) (US), Abcam (United Kingdom) (GB)
No poverty
Openalex Percentile: Top 8%
Single-cell and spatial transcriptomics
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