Evidence map›Paper›PMID 25619842›Full record

ArticleOncogene2015

SREBP maintains lipid biosynthesis and viability of cancer cells under lipid- and oxygen-deprived conditions and defines a gene signature associated with poor survival in glioblastoma multiforme.

C A Lewis, C Brault, B Peck, K Bensaad, B Griffiths, R Mitter, P Chakravarty, P East, B Dankworth, D Alibhai and 2 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 156 papers.

0numbers the graph read from it
0cells of the map it votes in
156citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

156 citing papers in PubMed, 237 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Article
  5. Article
  6. Accumulation of Siglec10European journal of immunology · 2026
    Article
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  8. Review
  9. Article
  10. Article
  11. Article
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  13. RUNX2 cooperates with SREBP1 to rewire cancer metabolism and promote aggressiveness.Journal of experimental & clinical cancer research : CR · 2025
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article

96 more citing papers are in PubMed but not listed here.

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

12 authors at 4 institutions in 2 countries.

C A LewisGene Expression Analysis Laboratory, Cancer Research UK London Research Institute, London, UK.
C BraultTheodor-Boveri-Institute, Biocenter, Am Hubland, Würzburg, Germany.
B PeckGene Expression Analysis Laboratory, Cancer Research UK London Research Institute, London, UK.
K BensaadCRUK Growth Factor Group, The Weatherall Institute of Molecular Medicine, University of Oxford, Headington, Oxford, UK.
B GriffithsGene Expression Analysis Laboratory, Cancer Research UK London Research Institute, London, UK.
R MitterBioinformatics and Biostatistics Service, Cancer Research UK London Research Institute, London, UK.
P ChakravartyBioinformatics and Biostatistics Service, Cancer Research UK London Research Institute, London, UK.
P EastBioinformatics and Biostatistics Service, Cancer Research UK London Research Institute, London, UK.
B DankworthTheodor-Boveri-Institute, Biocenter, Am Hubland, Würzburg, Germany.
D AlibhaiLight Microscopy Core, Cancer Research UK London Research Institute, London, UK.
A L HarrisCRUK Growth Factor Group, The Weatherall Institute of Molecular Medicine, University of Oxford, Headington, Oxford, UK.
A SchulzeGene Expression Analysis Laboratory, Cancer Research UK London Research Institute, London, UK.
Cancer Research UK · GBComprehensive Cancer Center Mainfranken · DEMRC Weatherall Institute of Molecular Medicine · GBUniversity of Oxford · GB

Funding

Cancer Research UK 11359Cancer Research UK 16466Cancer Research UK 18974
6 · The paper itself

Abstract

Oxygen and nutrient limitation are common features of the tumor microenvironment and are associated with cancer progression and induction of metastasis. The inefficient vascularization of tumor tissue also limits the penetration of other serum-derived factors, such as lipids and lipoproteins, which can be rate limiting for cell proliferation and survival. Here we have investigated the effect of hypoxia and serum deprivation on sterol regulatory element-binding protein (SREBP) activity and the expression of lipid metabolism genes in human glioblastoma multiforme (GBM) cancer cells. We found that SREBP transcriptional activity was induced by serum depletion both in normoxic and hypoxic cells and that activation of SREBP was required to maintain the expression of fatty acid and cholesterol metabolism genes under hypoxic conditions. Moreover, expression of stearoyl-CoA desaturase, the enzyme required for the generation of mono-unsaturated fatty acids, and fatty acid-binding protein 7, a regulator of glioma stem cell function, was strongly dependent on SREBP function. Inhibition of SREBP function blocked lipid biosynthesis in hypoxic cancer cells and impaired cell survival under hypoxia and in a three-dimensional spheroid model. Finally, gene expression analysis revealed that SREBP defines a gene signature that is associated with poor survival in glioblastoma.

Indexed as

Brain NeoplasmsCell HypoxiaCell LineCell SurvivalGlioblastomaHumansImmunohistochemistryLipid MetabolismOligonucleotide Array Sequence AnalysisPolymerase Chain ReactionProportional Hazards ModelsRNA, Small InterferingSterol Regulatory Element Binding Protein 1TranscriptomeTransfectionRNA, Small InterferingSREBF1 protein, humanSterol Regulatory Element Binding Protein 1

Identifiers

PMID25619842
OpenAlexW2022853846

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.