Evidence map›Paper›PMID 32946518›Full record

ArticlePloS one2020

Transcriptomics predicts compound synergy in drug and natural product treated glioblastoma cells.

Lavinia-Lorena Pruteanu, Liliya Kopanitsa, Dezső Módos, Edgars Kletnieks, Elena Samarova, Andreas Bender, Leonardo Dario Gomez, David Stanley Bailey

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Lavinia-Lorena PruteanuIOTA Pharmaceuticals Ltd, St Johns Innovation Centre, Cambridge, United Kingdom.ORCID 0000-0001-8277-1113
Liliya KopanitsaIOTA Pharmaceuticals Ltd, St Johns Innovation Centre, Cambridge, United Kingdom.ORCID 0000-0002-3752-2887
Dezső MódosDepartment of Chemistry, Centre for Molecular Informatics, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0001-9412-6867
Edgars KletnieksDepartment of Chemistry, Centre for Molecular Informatics, University of Cambridge, Cambridge, United Kingdom.ORCID 0000-0002-3735-7623
Elena SamarovaIOTA Pharmaceuticals Ltd, St Johns Innovation Centre, Cambridge, United Kingdom.ORCID 0000-0002-1443-6919
Andreas BenderDepartment of Chemistry, Centre for Molecular Informatics, University of Cambridge, Cambridge, United Kingdom.
Leonardo Dario GomezDepartment of Biology, Centre for Novel Agricultural Products, University of York, York, United Kingdom.ORCID 0000-0001-6382-9447
David Stanley BaileyIOTA Pharmaceuticals Ltd, St Johns Innovation Centre, Cambridge, United Kingdom.ORCID 0000-0002-9343-3408
University of Cambridge · GBUniversity of York · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathway analysis is an informative method for comparing and contrasting drug-induced gene expression in cellular systems. Here, we define the effects of the marine natural product fucoxanthin, separately and in combination with the prototypic phosphatidylinositol 3-kinase (PI3K) inhibitor LY-294002, on gene expression in a well-established human glioblastoma cell system, U87MG. Under conditions which inhibit cell proliferation, LY-294002 and fucoxanthin modulate many pathways in common, including the retinoblastoma, DNA damage, DNA replication and cell cycle pathways. In sharp contrast, we see profound differences in the expression of genes characteristic of pathways such as apoptosis and lipid metabolism, contributing to the development of a differentiated and distinctive drug-induced gene expression signature for each compound. Furthermore, in combination, fucoxanthin synergizes with LY-294002 in inhibiting the growth of U87MG cells, suggesting complementarity in their molecular modes of action and pointing to further treatment combinations. The synergy we observe between the dietary nutraceutical fucoxanthin and the synthetic chemical LY-294002 in producing growth arrest in glioblastoma, illustrates the potential of nutri-pharmaceutical combinations in targeting this challenging disease.

Indexed as

ApoptosisBiological ProductsCell Line, TumorCell ProliferationChromonesCombined Modality TherapyDietary SupplementsDrug SynergismGene Expression ProfilingGene Expression Regulation, NeoplasticGene Regulatory NetworksGlioblastomaHumansMorpholinesPhosphoinositide-3 Kinase InhibitorsXanthophylls2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-oneBiological ProductsChromonesfucoxanthinMorpholinesPhosphoinositide-3 Kinase InhibitorsXanthophylls

Identifiers

PMID32946518
PMCPMC7500592
OpenAlexW3087222131

What OpenQuestion holds

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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.