Evidence map›Paper›PMID 39576014›Full record

ArticleJCI insight2024

CRISPR/CasRx suppresses KRAS-induced brain arteriovenous malformation developed in postnatal brain endothelial cells in mice.

Shoji Saito, Yuka Nakamura, Satoshi Miyashita, Tokiharu Sato, Kana Hoshina, Masayasu Okada, Hitoshi Hasegawa, Makoto Oishi, Yukihiko Fujii, Jakob Körbelin and 4 more

Abstract read
In one paragraph

Article in JCI insight, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Towards precision medicine for brain arteriovenous malformations.The Journal of clinical investigation · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. 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.

Shoji SaitoDepartment of Neurosurgery and.
Yuka NakamuraDepartment of System Pathology for Neurological Disorders, Brain Research Institute, Niigata University, Niigata, Japan.
Satoshi MiyashitaDepartment of System Pathology for Neurological Disorders, Brain Research Institute, Niigata University, Niigata, Japan.
Tokiharu SatoDepartment of System Pathology for Neurological Disorders, Brain Research Institute, Niigata University, Niigata, Japan.
Kana HoshinaDepartment of System Pathology for Neurological Disorders, Brain Research Institute, Niigata University, Niigata, Japan.
Masayasu OkadaDepartment of Neurosurgery and.
Hitoshi HasegawaDepartment of Neurosurgery and.
Makoto OishiDepartment of Neurosurgery and.
Yukihiko FujiiDepartment of Neurosurgery and.
Jakob KörbelinDepartment of Oncology, Hematology and Bone Marrow Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Yoshiaki KubotaDepartment of Anatomy, Keio University School of Medicine, Tokyo, Japan.
Kazuki TainakaDepartment of System Pathology for Neurological Disorders, Brain Research Institute, Niigata University, Niigata, Japan.
Manabu NatsumedaDepartment of Neurosurgery and.
Masaki UenoDepartment of System Pathology for Neurological Disorders, Brain Research Institute, Niigata University, Niigata, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain arteriovenous malformations (bAVMs) are anomalies forming vascular tangles connecting the arteries and veins, which cause hemorrhagic stroke in young adults. Current surgical approaches are highly invasive, and alternative therapeutic methods are warranted. Recent genetic studies identified KRAS mutations in endothelial cells of bAVMs; however, the underlying process leading to malformation in the postnatal stage remains unknown. Here we established a mouse model of bAVM developing during the early postnatal stage. Among 4 methods tested, mutant KRAS specifically introduced in brain endothelial cells by brain endothelial cell-directed adeno-associated virus (AAV) and endothelial cell-specific Cdh5-CreERT2 mice successfully induced bAVMs in the postnatal period. Mutant KRAS led to the development of multiple vascular tangles and hemorrhage in the brain with increased MAPK/ERK signaling and growth in endothelial cells. Three-dimensional analyses in cleared tissue revealed dilated vascular networks connecting arteries and veins, similar to human bAVMs. Single-cell RNA-Seq revealed dysregulated gene expressions in endothelial cells and multiple cell types involved in the pathological process. Finally, we employed CRISPR/CasRx to knock down mutant KRAS expression, which efficiently suppressed bAVM development. The present model reveals pathological processes that lead to postnatal bAVMs and demonstrates the efficacy of therapeutic strategies with CRISPR/CasRx.

Indexed as

CRISPR-Cas SystemsDisease Models, AnimalEndothelial CellsIntracranial Arteriovenous MalformationsProto-Oncogene Proteins p21(ras)AnimalsBrainHumansMiceMutationHras protein, mouseProto-Oncogene Proteins p21(ras)Molecular pathologyMouse modelsNeurological disordersNeuroscience

Identifiers

PMID39576014
PMCPMC11601911

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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.