Evidence map›Paper›PMID 24348050›Full record

ArticleOncoTargets and therapy2013

Signal transduction molecule patterns indicating potential glioblastoma therapy approaches.

Maria Linda Cruceru, Ana-Maria Enciu, Adrian Claudiu Popa, Radu Albulescu, Monica Neagu, Cristiana Pistol Tanase, Stefan N Constantinescu

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

18 citing papers in PubMed, 27 citations in OpenAlex.

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  13. LncRNA MALAT1/miR-129 axis promotes glioma tumorigenesis by targeting SOX2.Journal of cellular and molecular medicine · 2018
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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

7 authors at 4 institutions in 2 countries.

Maria Linda CruceruCarol Davila University of Medicine and Pharmacy, Department of Cellular and Molecular Medicine, Bucharest, Romania.
Ana-Maria EnciuCarol Davila University of Medicine and Pharmacy, Department of Cellular and Molecular Medicine, Bucharest, Romania ; Victor Babes National Institute of Pathology, Bucharest, Romania ; Operational Sectorial Programme for Competitive Economic Growth Canbioprot at Victor Babes National Institute of Pathology, Bucharest, Romania.
Adrian Claudiu PopaCarol Davila University of Medicine and Pharmacy, Department of Cellular and Molecular Medicine, Bucharest, Romania ; Army Centre for Medical Research, Bucharest, Romania.
Radu AlbulescuVictor Babes National Institute of Pathology, Bucharest, Romania ; National Institute for Chemical Pharmaceutical R&D, Bucharest, Romania ; Operational Sectorial Programme for Competitive Economic Growth Canbioprot at Victor Babes National Institute of Pathology, Bucharest, Romania.
Monica NeaguVictor Babes National Institute of Pathology, Bucharest, Romania ; Operational Sectorial Programme for Competitive Economic Growth Canbioprot at Victor Babes National Institute of Pathology, Bucharest, Romania.
Cristiana Pistol TanaseVictor Babes National Institute of Pathology, Bucharest, Romania ; Operational Sectorial Programme for Competitive Economic Growth Canbioprot at Victor Babes National Institute of Pathology, Bucharest, Romania.
Stefan N Constantinescude Duve Institute, Université Catholique de Louvain, Brussels, Belgium ; Ludwig Institute for Cancer Research, Brussels, Belgium ; Operational Sectorial Programme for Competitive Economic Growth Canbioprot at Victor Babes National Institute of Pathology, Bucharest, Romania.
Institutul National Victor Babes · ROCarol Davila University of Medicine and Pharmacy · ROLudwig Cancer Research · BENational Institute For Chemical Pharmaceutical Research and Development · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe expression of an array of signaling molecules, along with the assessment of real-time cell proliferation, has been performed in U87 glioma cell line and in patients' glioblastoma established cell cultures in order to provide a better understanding of cellular and molecular events involved in glioblastoma pathogenesis. Experimental therapy was performed using a phosphatidylinositol-3'-kinase (PI3K) inhibitor. PATIENTS AND

methodsxMAP technology was employed to assess expression levels of several signal transduction molecules and real-time xCELLigence platform for cell behavior.

resultsPI3K inhibition induced the most significant effects on global signaling pathways in patient-derived cell cultures, especially on members of the mitogen-activated protein-kinase family, P70S6 serine-threonine kinase, and cAMP response element-binding protein expression and further prevented tumor cell proliferation.

conclusionThe PI3K pathway might be a prime target for glioblastoma treatment.

Indexed as

personalized medicinePI3K inhibitortargeted therapyxCELLigencexMAP analysis

Identifiers

PMID24348050
PMCPMC3848931
OpenAlexW1979420536

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.