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April 5, 2026Cancer Research0 citations

Abstract 7191: 6-thio-dG enhances standard-of-care radiation therapy by reprogramming the tumor microenvironment in glioblastoma multiforme

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AGAnthony Alexander GrichukMYMerve YilmazSBSummer Barron

Key Points

  • The research assesses the potential of 6-thio-dG to enhance the effects of radiation therapy in glioblastoma by modifying the tumor microenvironment.
  • Utilized glioblastoma models for treatment with 6-thio-dG and ionizing radiation (IR) combinations.
  • Assessed immune signaling and microglia/macrophage phenotypes through molecular and histological analyses.
  • Performed functional analyses to evaluate tumor responses to treatments.
  • Sequential treatment of 6-thio-dG followed by IR markedly increased type I interferon (IFN-I) activation.
  • The treatment shifted microglia/macrophages to a pro-inflammatory M1 phenotype.
  • Combination therapy demonstrated a significant anti-tumor effect compared to monotherapy.

Abstract

Abstract Background/Objectives- Glioblastoma multiforme (GBM) remains highly lethal, with a five-year survival rate of only 6.9%. Standard-of-care treatments such as ionizing radiation (IR) and temozolomide frequently fail to produce durable responses due to poor drug penetration across the blood-brain barrier (BBB) and the immunosuppressive tumor microenvironment (TME). 6-thio-2′-deoxyguanosine (6-thio-dG) is a telomerase-mediated telomere-targeting guanine analog that induces telomeric DNA damage selectively in telomerase-positive tumor cells. This process activates the cGAS-STING pathway, triggers innate and adaptive immune responses and has previously resensitized resistant tumors to immunotherapy in a Phase 2 NSCLC clinical trial. We hypothesized that 6-thio-dG penetrates the BBB and enhances the therapeutic efficacy of IR by reprogramming the GBM TME. Methods- GBM models were treated with 6-thio-dG alone, IR alone, or sequential 6-thio-dG followed by IR. Immune signaling, microglia/macrophage phenotypes, and tumor responses were assessed via molecular, histological, and functional analyses. Results- Sequential 6-thio-dG + IR treatment significantly increased type I interferon (IFN-I) activation and shifted microglia/macrophages toward a pro-inflammatory M1 phenotype. This TME reprogramming resulted in a statistically significant anti-tumor effect relative to monotherapy. Conclusions- 6-thio-dG enhances IR efficacy in GBM by inducing telomere-driven immune activation and promoting an anti-tumor TME. These findings support 6-thio-dG as a promising adjuvant to standard-of-care and justify further investigation of telomere-targeted combination strategies. Citation Format: Anthony Alexander Grichuk, Merve Yilmaz, Summer Barron, Priya Darbha, Shannon M. McCabe, Jerry W. Shay, Kristin Huntoon. 6-thio-dG enhances standard-of-care radiation therapy by reprogramming the tumor microenvironment in glioblastoma multiforme 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 7191.

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Grichuk et al. (2026) studied this question.

synapsesocial.com/papers/69d1fceba79560c99a0a2ac8https://doi.org/10.1158/1538-7445.am2026-7191
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Abstract 5108: Immunomodulatory and anti-tumor effect of radiation and induced telomere damage to treat pediatric high-grade gliomas2024
  2. 2DMG-22. Induced telomere damage and cell cycle checkpoint blockade: a novel approach for radiosensitization and immunomodulation to treat diffuse midline glioma2025
  3. 3Abstract B051: DNA damage signaling activates GTP synthesis to promote glioblastoma treatment resistance2024
  4. 4Abstract 2037: Enhanced chemosensitivity to DNA-damaging agents in human high-grade glioma through 2-DG treatment2024
  5. 5INB-200: Phase I study and characterization of gene-modified autologous gamma delta (γδ) T cells in newly diagnosed glioblastoma multiforme (GBM).2026