Evidence map›Paper›PMID 38760945›Full record

ArticleBioFactors (Oxford, England)

Anticancer effect of minor phytocannabinoids in preclinical models of multiple myeloma.

Cristina Aguzzi, Laura Zeppa, Maria Beatrice Morelli, Oliviero Marinelli, Martina Giangrossi, Consuelo Amantini, Giorgio Santoni, Hossain Sazzad, Massimo Nabissi

Abstract read
In one paragraph

Article in BioFactors (Oxford, England). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. 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

9 authors.

Cristina AguzziSchool of Pharmacy, University of Camerino, Camerino, MC, Italy.
Laura ZeppaSchool of Pharmacy, University of Camerino, Camerino, MC, Italy.
Maria Beatrice MorelliSchool of Pharmacy, University of Camerino, Camerino, MC, Italy.
Oliviero MarinelliSchool of Pharmacy, University of Camerino, Camerino, MC, Italy.
Martina GiangrossiSchool of Pharmacy, University of Camerino, Camerino, MC, Italy.
Consuelo AmantiniSchool of Bioscience and Veterinary Medicine, University of Camerino, Camerino, MC, Italy.
Giorgio SantoniSchool of Pharmacy, University of Camerino, Camerino, MC, Italy.
Hossain SazzadEntourage Biosciences Inc., Vancouver, Canada.
Massimo NabissiSchool of Pharmacy, University of Camerino, Camerino, MC, Italy.ORCID https://orcid.org/0000-0003-0165-1385

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a blood cancer caused by uncontrolled growth of clonal plasmacells. Bone disease is responsible for the severe complications of MM and is caused by myeloma cells infiltrating the bone marrow and inducing osteoclast activation. To date, no treatment for MM is truly curative since patients relapse and become refractory to all drug classes. Cannabinoids are already used as palliative in cancer patients. Furthermore, their proper anticancer effect was demonstrated in many cancer models in vitro, in vivo, and in clinical trials. Anyway, few information was reported on the effect of cannabinoids on MM and no data has been provided on minor phytocannabinoids such as cannabigerol (CBG), cannabichromene (CBC), cannabinol (CBN), and cannabidivarin (CBDV). Scientific literature also reported cannabinoids beneficial effect against bone disease. Here, we examined the cytotoxic activity of CBG, CBC, CBN, and CBDV in vitro in MM cell lines, their effect in modulating MM cells invasion toward bone cells and the bone resorption. Subsequently, according to the in vitro results, we selected CBN for in vivo study in a MM xenograft mice model. Results showed that the phytocannabinoids inhibited MM cell growth and induced necrotic cell death. Moreover, the phytocannabinoids reduced the invasion of MM cells toward osteoblast cells and bone resorption in vitro. Lastly, CBN reduced in vivo tumor mass. Together, our results suggest that CBG, CBC, CBN, and CBDV can be promising anticancer agents for MM.

Indexed as

CannabinoidsMultiple MyelomaXenograft Model Antitumor AssaysAnimalsAntineoplastic Agents, PhytogenicBone ResorptionCell Line, TumorCell ProliferationHumansMiceAntineoplastic Agents, PhytogenicCannabinoidsbone lesioncell invasionmultiple myelomaphytocannabinoids

Identifiers

PMID38760945
PMCPMC11627469

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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.