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

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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Journal
Cancer Research
Published
2026-04-03
DOI
https://doi.org/10.1158/1538-7445.am2026-7191
Primary Topic
interferon and immune responses
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article
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article

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

J. W. Shay, Summer Barron, Kristin Michelle Huntoon, Priya Darbha et al.
Cancer Research
interferon and immune responses
article

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

J. W. Shay, Summer Barron, Kristin Michelle Huntoon, Priya Darbha, Shannon M. McCabe, Merve Yilmaz, Anthony Alexander Grichuk
article en

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.

Cancer ResearchVol. 86(7_Supplement)
University of Arizona (US), Dallas County (US), Southwestern Medical Center (US), The University of Texas Southwestern Medical Center (US)
Openalex Percentile: Top 8%
interferon and immune responses
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