Evidence map›Paper›PMID 38794334›Full record

ArticlePharmaceutics2024

The Proteasome Inhibitor CEP-18770 Induces Cell Death in Medulloblastoma.

Swastina Nath Varma, Shany Ye, Sara Ferlin, Charley Comer, Kian Cotton, Maria Victoria Niklison-Chirou

Abstract read
In one paragraph

Article in Pharmaceutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

6 authors.

Swastina Nath VarmaBlizard Institute, Queen Mary University of London, London E1 4NS, UK.ORCID 0000-0002-9449-8772
Shany YeLife Sciences Department, University of Bath, Claverton Down, Bath BA2 7AY, UK.ORCID 0009-0006-5584-1845
Sara FerlinLife Sciences Department, University of Bath, Claverton Down, Bath BA2 7AY, UK.
Charley ComerLife Sciences Department, University of Bath, Claverton Down, Bath BA2 7AY, UK.ORCID 0009-0002-9699-9498
Kian CottonLife Sciences Department, University of Bath, Claverton Down, Bath BA2 7AY, UK.ORCID 0009-0008-5551-9412
Maria Victoria Niklison-ChirouBlizard Institute, Queen Mary University of London, London E1 4NS, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Medulloblastomas (MBs) represent the most prevalent malignant solid tumors in kids. The conventional treatment regimen for MBs includes surgical removal of the tumor, followed by radiation and chemotherapy. However, this approach is associated with significant morbidity and detrimental side effects. Consequently, there is a critical demand for more precise and less harmful treatments to enhance the quality of life for survivors. CEP-18770, a novel proteasome inhibitor that targets the 20S subunit, has emerged as a promising candidate, due to its anticancer activity in metastatic solid tumors and multiple myeloma, coupled with an acceptable safety profile. In this study, we aimed to assess the anticancer efficacy of CEP-18770 by employing a variety of MB patient-derived cells and cell lines. Our preclinical investigations revealed that CEP-18770 effectively inhibits proteasome activity and induces apoptosis in MBs cells. Furthermore, we discovered that CEP-18770 and cisplatin, a current component of MB therapy, exhibit a synergistic apoptotic effect. This paper shows that CEP-18770 holds potential as an adjunctive treatment for MB tumors, thereby paving the way for more targeted and less toxic therapeutic strategies.

Indexed as

brain tumorscancerCEP-18770medulloblastomaproteasome inhibitors

Identifiers

PMID38794334
PMCPMC11124782

What OpenQuestion holds

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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.