Evidence map›Paper›PMID 25400117›Full record

ArticleOncotarget2014

Proscillaridin A is cytotoxic for glioblastoma cell lines and controls tumor xenograft growth in vivo.

Emilie Denicolaï, Nathalie Baeza-Kallee, Aurélie Tchoghandjian, Manon Carré, Carole Colin, Carine Jiguet Jiglaire, Sandy Mercurio, Christophe Beclin, Dominique Figarella-Branger

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

28 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. PBI-05204, a supercritical CONeoplasia (New York, N.Y.) · 2024
    Article
  3. Article
  4. Deciphering the Action of Neuraminidase in Glioblastoma Models.International journal of molecular sciences · 2023
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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

9 authors at 3 institutions in 1 country.

Emilie DenicolaïInserm, Aix-Marseille Université, CRO2 UMR_S 911, Marseille, 13385, France.
Nathalie Baeza-KalleeInserm, Aix-Marseille Université, CRO2 UMR_S 911, Marseille, 13385, France.
Aurélie TchoghandjianInserm, Aix-Marseille Université, CRO2 UMR_S 911, Marseille, 13385, France.
Manon CarréInserm, Aix-Marseille Université, CRO2 UMR_S 911, Marseille, 13385, France.
Carole ColinInserm, Aix-Marseille Université, CRO2 UMR_S 911, Marseille, 13385, France.
Carine Jiguet JiglaireInserm, Aix-Marseille Université, CRO2 UMR_S 911, Marseille, 13385, France.
Sandy MercurioInserm, Aix-Marseille Université, CRO2 UMR_S 911, Marseille, 13385, France.
Christophe BeclinCNRS, IBDML, Aix Marseille Université, UMR_S 6216, Marseille, 13288, France.
Dominique Figarella-BrangerInserm, Aix-Marseille Université, CRO2 UMR_S 911, Marseille, 13385, France. APHM, Hôpital de la Timone, Service d'Anatomie Pathologique et de Neuropathologie, Marseille, 13385, France.
Aix-Marseille Université · FRInserm · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma is the most frequent primary brain tumor in adults. Because of molecular and cellular heterogeneity, high proliferation rate and significant invasive ability, prognosis of patients is poor. Recent therapeutic advances increased median overall survival but tumor recurrence remains inevitable. In this context, we used a high throughput screening approach to bring out novel compounds with anti-proliferative and anti-migratory properties for glioblastoma treatment. Screening of the Prestwick chemical library® of 1120 molecules identified proscillaridin A, a cardiac glycoside inhibitor of the Na(+)/K(+) ATPase pump, with most significant effects on glioblastoma cell lines. In vitro effects of proscillaridin A were evaluated on GBM6 and GBM9 stem-like cell lines and on U87-MG and U251-MG cell lines. We showed that proscillaridin A displayed cytotoxic properties, triggered cell death, induced G2/M phase blockade in all the glioblastoma cell lines and impaired GBM stem self-renewal capacity even at low concentrations. Heterotopic and orthotopic xenotransplantations were used to confirm in vivo anticancer effects of proscillaridin A that both controls xenograft growth and improves mice survival. Altogether, results suggest that proscillaridin A is a promising candidate as cancer therapies in glioblastoma. This sustains previous reports showing that cardiac glycosides act as anticancer drugs in other cancers.

Indexed as

AdultAnimalsApoptosisBlotting, WesternBrain NeoplasmsCell CycleCell MovementCell ProliferationEnzyme InhibitorsFemaleGene Expression ProfilingGlioblastomaHigh-Throughput Screening AssaysHumansImmunoenzyme TechniquesMiceEnzyme InhibitorsProscillaridinRNA, Messenger

Identifiers

PMID25400117
PMCPMC4279420
OpenAlexW1945903691

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.