Evidence map›Paper›PMID 33477420›Full record

ArticleCancers2021

Assessment of Cannabidiol and Δ9-Tetrahydrocannabiol in Mouse Models of Medulloblastoma and Ependymoma.

Clara Andradas, Jacob Byrne, Mani Kuchibhotla, Mathew Ancliffe, Anya C Jones, Brooke Carline, Hilary Hii, Alexandra Truong, Lisa C D Storer, Timothy A Ritzmann and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.6field-weighted citation impact, top 8% of its field
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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Medical Cannabis and the Hallmarks of Cancer: A Critical Narrative Review.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Review
  4. Gene replacement therapy in a schwannoma mouse model of neurofibromatosis type 2.Molecular therapy. Methods & clinical development · 2022
    Article
  5. Review
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  7. Review
  8. Article
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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

13 authors at 2 institutions in 2 countries.

Clara AndradasBrain Tumour Research Program, Telethon Kids Institute, Nedlands, WA 6009, Australia.ORCID 0000-0003-4655-0932
Jacob ByrneBrain Tumour Research Program, Telethon Kids Institute, Nedlands, WA 6009, Australia.
Mani KuchibhotlaBrain Tumour Research Program, Telethon Kids Institute, Nedlands, WA 6009, Australia.
Mathew AncliffeBrain Tumour Research Program, Telethon Kids Institute, Nedlands, WA 6009, Australia.
Anya C JonesTelethon Kids Cancer Centre, Telethon Kids Institute, Nedlands, WA 6009, Australia.
Brooke CarlineBrain Tumour Research Program, Telethon Kids Institute, Nedlands, WA 6009, Australia.ORCID 0000-0002-8061-4170
Hilary HiiBrain Tumour Research Program, Telethon Kids Institute, Nedlands, WA 6009, Australia.
Alexandra TruongBrain Tumour Research Program, Telethon Kids Institute, Nedlands, WA 6009, Australia.ORCID 0000-0002-9233-8273
Lisa C D StorerChildren's Brain Tumour Research Centre, University of Nottingham, Nottingham NG7 2RD, UK.
Timothy A RitzmannChildren's Brain Tumour Research Centre, University of Nottingham, Nottingham NG7 2RD, UK.ORCID 0000-0002-4438-6588
Richard G GrundyChildren's Brain Tumour Research Centre, University of Nottingham, Nottingham NG7 2RD, UK.
Nicholas G GottardoBrain Tumour Research Program, Telethon Kids Institute, Nedlands, WA 6009, Australia.
Raelene EndersbyBrain Tumour Research Program, Telethon Kids Institute, Nedlands, WA 6009, Australia.ORCID 0000-0003-3554-2769
The Kids Research Institute Australia · AUUniversity of Nottingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Children with medulloblastoma and ependymoma are treated with a multidisciplinary approach that incorporates surgery, radiotherapy, and chemotherapy; however, overall survival rates for patients with high-risk disease remain unsatisfactory. Data indicate that plant-derived cannabinoids are effective against adult glioblastoma; however, preclinical evidence supporting their use in pediatric brain cancers is lacking. Here we investigated the potential role for Δ9-tetrahydrocannabinol (THC) and cannabidiol (CBD) in medulloblastoma and ependymoma. Dose-dependent cytotoxicity of medulloblastoma and ependymoma cells was induced by THC and CBD in vitro, and a synergistic reduction in viability was observed when both drugs were combined. Mechanistically, cannabinoids induced cell cycle arrest, in part by the production of reactive oxygen species, autophagy, and apoptosis; however, this did not translate to increased survival in orthotopic transplant models despite being well tolerated. We also tested the combination of cannabinoids with the medulloblastoma drug cyclophosphamide, and despite some in vitro synergism, no survival advantage was observed in vivo. Consequently, clinical benefit from the use of cannabinoids in the treatment of high-grade medulloblastoma and ependymoma is expected to be limited. This study emphasizes the importance of preclinical models in validating therapeutic agent efficacy prior to clinical trials, ensuring that enrolled patients are afforded the most promising therapies available.

Indexed as

cannabidiolcannabinoidCBDchildhood cancerependymomamedical cannabismedulloblastomapediatric oncologyTHCΔ9-tetrahydrocannabinol

Identifiers

PMID33477420
PMCPMC7829707
OpenAlexW3121789320

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.