Evidence map›Paper›PMID 30565681›Full record

ArticleThe Journal of pathology2019

shRNA-mediated PPARα knockdown in human glioma stem cells reduces in vitro proliferation and inhibits orthotopic xenograft tumour growth.

Harry R Haynes, Helen L Scott, Clare L Killick-Cole, Gary Shaw, Tim Brend, Kelly M Hares, Juliana Redondo, Kevin C Kemp, Lorena S Ballesteros, Andrew Herman and 11 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Modeling pediatric brain tumors with human stem cells.Frontiers in cellular neuroscience · 2026
    Review
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  14. A Shifty Target: Tumor-Initiating Cells and Their Metabolism.International journal of molecular sciences · 2019
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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

21 authors at 4 institutions in 1 country.

Harry R HaynesBrain Tumour Research Group, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.ORCID 0000-0001-6468-7671
Helen L ScottTranslational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Clare L Killick-ColeFunctional Neurosurgery Research Group, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Gary ShawLeeds Institute of Cancer and Pathology, University of Leeds, Leeds, UK.
Tim BrendLeeds Institute of Cancer and Pathology, University of Leeds, Leeds, UK.
Kelly M HaresMultiple Sclerosis and Stem Cell Group, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Juliana RedondoMultiple Sclerosis and Stem Cell Group, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Kevin C KempMultiple Sclerosis and Stem Cell Group, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Lorena S BallesterosFlow Cytometry Facility, School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Andrew HermanFlow Cytometry Facility, School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.
Oscar Cordero-LlanaTranslational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
William G SingletonFunctional Neurosurgery Research Group, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Francesca MillsDepartment of Clinical Biochemistry, North Bristol NHS Trust, Bristol, UK.
Tom BatstoneBioinformatics Facility, School of Biological Sciences, University of Bristol, Bristol, UK.
Harry BulstrodeDepartment of Clinical Neuroscience and Stem Cell Institute, University of Cambridge, Cambridge, UK.
Risto A KauppinenClinical Research and Imaging Centre, University of Bristol, Bristol, UK.
Heiko WurdakStem Cells and Brain Tumour Group, Leeds Institute of Cancer and Pathology, University of Leeds, Leeds, UK.
James B UneyTranslational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Susan C ShortLeeds Institute of Cancer and Pathology, University of Leeds, Leeds, UK.
Alastair WilkinsMultiple Sclerosis and Stem Cell Group, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Kathreena M KurianBrain Tumour Research Group, Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
University of Bristol · GBUniversity of Leeds · GBNorth Bristol NHS Trust · GBWellcome/MRC Cambridge Stem Cell Institute · GB

Funding

Biotechnology and Biological Sciences Research Council (BBSRC) BB/M017532Cancer Research UK 10065Medical Research Council G0701018Medical Research Council G1100578Medical Research Council MR/N001370/1Medical Research Council MR/N004272/1
6 · The paper itself

Abstract

The overall survival for patients with primary glioblastoma is very poor. Glioblastoma contains a subpopulation of glioma stem cells (GSC) that are responsible for tumour initiation, treatment resistance and recurrence. PPARα is a transcription factor involved in the control of lipid, carbohydrate and amino acid metabolism. We have recently shown that PPARα gene and protein expression is increased in glioblastoma and has independent clinical prognostic significance in multivariate analyses. In this work, we report that PPARα is overexpressed in GSC compared to foetal neural stem cells. To investigate the role of PPARα in GSC, we knocked down its expression using lentiviral transduction with short hairpin RNA (shRNA). Transduced GSC were tagged with luciferase and stereotactically xenografted into the striatum of NOD-SCID mice. Bioluminescent and magnetic resonance imaging showed that knockdown (KD) of PPARα reduced the tumourigenicity of GSC in vivo. PPARα-expressing control GSC xenografts formed invasive histological phenocopies of human glioblastoma, whereas PPARα KD GSC xenografts failed to establish viable intracranial tumours. PPARα KD GSC showed significantly reduced proliferative capacity and clonogenic potential in vitro with an increase in cellular senescence. In addition, PPARα KD resulted in significant downregulation of the stem cell factors c-Myc, nestin and SOX2. This was accompanied by downregulation of the PPARα-target genes and key regulators of fatty acid oxygenation ACOX1 and CPT1A, with no compensatory increase in glycolytic flux. These data establish the aberrant overexpression of PPARα in GSC and demonstrate that this expression functions as an important regulator of tumourigenesis, linking self-renewal and the malignant phenotype in this aggressive cancer stem cell subpopulation. We conclude that targeting GSC PPARα expression may be a therapeutically beneficial strategy with translational potential as an adjuvant treatment. © 2018 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

Indexed as

AnimalsBiomarkers, TumorBrain NeoplasmsCell Transformation, NeoplasticDown-RegulationFemaleGene Expression Regulation, NeoplasticGene Knockdown TechniquesGlioblastomaHumansLentivirusMice, Inbred NODMice, SCIDNeoplastic Stem CellsPhenotypePPAR alphaBiomarkers, TumorPPAR alphaRNA, Small Interferingglioma stem cellPPARαshRNA

Identifiers

PMID30565681
PMCPMC6462812
OpenAlexW2904338396

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.