Evidence map›Paper›PMID 41979168›Full record

ArticleOncoimmunology2026

PARP7 inhibition and a STING agonist potentiate radiation-induced immunogenicity in glioblastoma.

Luca Lippert, Ava Kleinwächter, Anna Ohradanova-Repic, Filip Horvat, Lisa-Marie Appel, Lena Walch, Niccolò Bragato, Jakob Wimmer, Hanna Wopfner, Anna Röhrer and 5 more

Abstract read
In one paragraph

Article in Oncoimmunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Luca LippertDepartment of Radiation Oncology, Medical University of Vienna, Vienna, Austria.
Ava KleinwächterDepartment of Radiation Oncology, Medical University of Vienna, Vienna, Austria.
Anna Ohradanova-RepicMedical University of Vienna, Center for Pathophysiology, Infectiology and Immunology, Institute for Hygiene and Applied Immunology, Vienna, Austria.
Filip HorvatDepartment of Radiation Oncology, Medical University of Vienna, Vienna, Austria.
Lisa-Marie AppelDepartment of Radiation Oncology, Medical University of Vienna, Vienna, Austria.
Lena WalchDepartment of Radiation Oncology, Medical University of Vienna, Vienna, Austria.
Niccolò BragatoDepartment of Radiation Oncology, Medical University of Vienna, Vienna, Austria.
Jakob WimmerDepartment of Radiation Oncology, Medical University of Vienna, Vienna, Austria.
Hanna WopfnerDepartment of Radiation Oncology, Medical University of Vienna, Vienna, Austria.
Anna RöhrerDepartment of Radiation Oncology, Medical University of Vienna, Vienna, Austria.
Magdalena EnglDepartment of Radiation Oncology, Medical University of Vienna, Vienna, Austria.
Kapil UpadhyayaDepartment of Chemical Physiology and Biochemistry, Oregon Health and Science University, Portland, OR, USA.
Joachim WidderDepartment of Radiation Oncology, Medical University of Vienna, Vienna, Austria.
Michael S CohenDepartment of Chemical Physiology and Biochemistry, Oregon Health and Science University, Portland, OR, USA.
Dea SladeDepartment of Radiation Oncology, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-0052-5910

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is the most lethal form of brain cancer with an immunosuppressive tumor microenvironment (TME). Radio- and chemotherapy can modify the TME and elicit anti-tumor immunity through the STING and type I interferon (IFN-I) pathways. STING agonists or DNA damage response inhibitors can potentiate the effects of radiation by targeting the IFN-I pathway. Here, we examined the immunogenic response of GBM cells to hypofractionated or single-dose radiation combined with a STING agonist or inhibitors targeting immune signaling (PARP7), the DNA damage response, cell cycle checkpoints or autophagy. We found that hypofractionated radiation elicited a ferroptosis-dependent IFN-I response and that the PARP7 inhibitor KMR-206 and the STING agonist diABZI enhanced the effects of radiation by activating immune cells. In patient-derived GBM cancer stem cells with low STING levels, the PARP7 inhibitor was more effective at inducing immunogenic signaling compared to the STING agonist. Our results highlight the potential of PARP7 inhibitors as a new treatment to boost anti-tumor immunity in GBM, which may be more advantageous compared to STING agonists given that STING is often downregulated in GBM.

Indexed as

Brain NeoplasmsGlioblastomaMembrane ProteinsPoly(ADP-ribose) Polymerase InhibitorsAnimalsCell Line, TumorcGAS-STING Signaling PathwayHumansInterferon Type IMiceNeoplastic Stem CellsSignal TransductionSTING ProteinTumor MicroenvironmentInterferon Type IMembrane ProteinsPoly(ADP-ribose) Polymerase InhibitorsSTING1 protein, humanSTING ProteinGlioblastomaIFN-I responsePARP7radiationSTING agonist

Identifiers

PMID41979168
PMCPMC13081750

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.