Evidence map›Paper›PMID 33562819›Full record

ArticleCells2021

Cannabigerol Is a Potential Therapeutic Agent in a Novel Combined Therapy for Glioblastoma.

Tamara T Lah, Metka Novak, Milagros A Pena Almidon, Oliviero Marinelli, Barbara Žvar Baškovič, Bernarda Majc, Mateja Mlinar, Roman Bošnjak, Barbara Breznik, Roby Zomer and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 1 pooled it
11.6field-weighted citation impact, top 1% 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

58 citing papers in PubMed, 1 synthesis or guideline pooled it, 93 citations in OpenAlex.

  1. Pooled it
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  11. Review
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  13. Review
  14. Cannabigerol ExertsJournal of microbiology and biotechnology · 2025
    Article
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  17. 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

11 authors at 5 institutions in 2 countries.

Tamara T LahDepartment of Genetic Toxicology and Cancer Biology, National Institute of Biology, 1000 Ljubljana, Slovenia.
Metka NovakDepartment of Genetic Toxicology and Cancer Biology, National Institute of Biology, 1000 Ljubljana, Slovenia.
Milagros A Pena AlmidonSchool of Pharmacy, Experimental Medicine Section, University of Camerino, 62032 Camerino, Italy.
Oliviero MarinelliSchool of Pharmacy, Experimental Medicine Section, University of Camerino, 62032 Camerino, Italy.ORCID 0000-0001-5518-5303
Barbara Žvar BaškovičDepartment of Genetic Toxicology and Cancer Biology, National Institute of Biology, 1000 Ljubljana, Slovenia.
Bernarda MajcDepartment of Genetic Toxicology and Cancer Biology, National Institute of Biology, 1000 Ljubljana, Slovenia.
Mateja MlinarDepartment of Genetic Toxicology and Cancer Biology, National Institute of Biology, 1000 Ljubljana, Slovenia.
Roman BošnjakDepartment of Neurosurgery, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.
Barbara BreznikDepartment of Genetic Toxicology and Cancer Biology, National Institute of Biology, 1000 Ljubljana, Slovenia.ORCID 0000-0003-0247-5811
Roby ZomerMGC Pharmaceuticals d.o.o., 1000 Ljubljana, Slovenia.
Massimo NabissiSchool of Pharmacy, Experimental Medicine Section, University of Camerino, 62032 Camerino, Italy.ORCID 0000-0003-0165-1385
National Institute of Biology · SIUniversità di Camerino · ITJožef Stefan International Postgraduate School · SILjubljana University Medical Centre · SIUniversity of Ljubljana · SI

Funding

European Program of Cross-Border Cooperation for Slovenia-Italy Interreg TRANS-GLIOMA to T.T.L.MGC Pharmaceuticals to T.T.L.Slovenian Research Agency Grant Program P1-0245 to T.T.L.Slovenian Research Agency post-doctoral project Z3-1870 to B.B.
6 · The paper itself

Abstract

Glioblastoma is the most aggressive cancer among primary brain tumours. As with other cancers, the incidence of glioblastoma is increasing; despite modern therapies, the overall mean survival of patients post-diagnosis averages around 16 months, a figure that has not changed in many years. Cannabigerol (CBG) has only recently been reported to prevent the progression of certain carcinomas and has not yet been studied in glioblastoma. Here, we have compared the cytotoxic, apoptotic, and anti-invasive effects of the purified natural cannabinoid CBG together with CBD and THC on established differentiated glioblastoma tumour cells and glioblastoma stem cells. CBG and THC reduced the viability of both types of cells to a similar extent, whereas combining CBD with CBG was more efficient than with THC. CBD and CBG, both alone and in combination, induced caspase-dependent cell apoptosis, and there was no additive THC effect. Of note, CBG inhibited glioblastoma invasion in a similar manner to CBD and the chemotherapeutic temozolomide. We have demonstrated that THC has little added value in combined-cannabinoid glioblastoma treatment, suggesting that this psychotropic cannabinoid should be replaced with CBG in future clinical studies of glioblastoma therapy.

Indexed as

ApoptosisBrain NeoplasmsCannabinoidsFemaleGlioblastomaHumanscannabigerolCannabinoidsapoptosiscannabidiolcannabigerolcannabinoidsdelta-9-tetrahydrocannabinolglioblastomainvasiontemozolomide

Identifiers

PMID33562819
PMCPMC7914500
OpenAlexW3127904902

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.