Evidence map›Paper›PMID 40594881›Full record

ArticleNPJ precision oncology2025

Dual treatment with Val-083 and AZD1775 shows potent anti-tumor activity in diffuse midline glioma models.

Bavani Subramaniam, Debasish Roy, Ayda Woldegerima, Wai Chin Chong, Justyna M Przystal, Jie Zhang, Sandra Laternser, Bettina Kritzer, Suraj Rangnath, Truman Knowles and 4 more

Abstract read
In one paragraph

Article in NPJ precision oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

14 authors.

Bavani SubramaniamBrain Tumor Institute, Center for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Debasish RoyBrain Tumor Institute, Center for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Ayda WoldegerimaBrain Tumor Institute, Center for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Wai Chin ChongBrain Tumor Institute, Center for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Justyna M PrzystalChildren's Research Center, University Children's Hospital Zurich, Zurich, Switzerland.
Jie ZhangDepartment of Neurology, University of California San Francisco, San Francisco, CA, USA.
Sandra LaternserChildren's Research Center, University Children's Hospital Zurich, Zurich, Switzerland.
Bettina KritzerChildren's Research Center, University Children's Hospital Zurich, Zurich, Switzerland.
Suraj RangnathUniversity of Michigan, Ann Arbor, MI, USA.
Truman KnowlesDepartment of Neurology, University of California San Francisco, San Francisco, CA, USA.
Sridevi YadavilliBrain Tumor Institute, Center for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Roger PackerBrain Tumor Institute, Center for Cancer and Immunology Research, Children's National Hospital, Washington, DC, USA.
Sabine MuellerChildren's Research Center, University Children's Hospital Zurich, Zurich, Switzerland.
Javad NazarianChildren's Research Center, University Children's Hospital Zurich, Zurich, Switzerland. javad.nazarian@kispi.uzh.ch.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

H3K27M diffuse midline gliomas (DMG) are characterized by p53 mutations and hypomethylation of MGMT, a DNA-repair enzyme, leading to resistance towards chemotherapeutic agents such as temozolomide (TMZ). As an alternative, we investigated the efficacy of a functionally different DNA-damaging agent, Val-083, on our DMG models. Val-083 is a blood-brain barrier penetrant DNA targeting agent that induces DNA N7-guanine interstrand crosslinks, which is unrepairable by MGMT. As Val-083 also triggers S/G2 phase cell cycle arrest for DNA repair, we evaluated its combined efficacy with Wee1 inhibitor, AZD1775. AZD1775 functions by inhibiting Wee1, at G2/M checkpoint to prevent phosphorylation of CDK1 and propel cells into the M phase. This subsequently overrides cell cycle arrest and drives cells with DNA damage into premature mitosis and apoptosis. Our results showed that Val-083 and AZD1775 work additively on a range of p53 mutant and p53 wildtype DMG models to inhibit cell growth, induce DNA damage and alter cell cycle. In addition, the combination drugs led to significant increase in the number of cells undergoing apoptosis, and a decrease in the migration and invasion activity of the cells. In vivo, the combination of both drugs led to significant reduction in tumor growth in zebrafish xenograft models and prolongation of survival in mice xenograft models. Our findings indicate that Val-083 and AZD1775 in combination demonstrate promising efficacy in DMGs, providing a clinical rationale for positioning these arms in future therapies.

Identifiers

PMID40594881
PMCPMC12215462

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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.