Evidence map›Paper›PMID 35213227›Full record

ArticleScience advances2022

Metabolic profiling of prostate cancer in skeletal microenvironments identifies G6PD as a key mediator of growth and survival.

Jessica Whitburn, Srinivasa R Rao, Emma V Morris, Sho Tabata, Akiyoshi Hirayama, Tomoyoshi Soga, James R Edwards, Zeynep Kaya, Charlotte Palmer, Freddie C Hamdy and 1 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

32 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
  3. Metabolism in Tumour-Induced Bone Disease.Current osteoporosis reports · 2026
    Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Metabolic adaptations in prostate cancer.British journal of cancer · 2024
    Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Review
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

11 authors at 3 institutions in 2 countries.

Jessica WhitburnNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.ORCID 0000-0001-8320-7725
Srinivasa R RaoNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.ORCID 0000-0003-1889-6530
Emma V MorrisNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.
Sho TabataInstitute for Advanced Biosciences, Keio University, Yamagata, Japan.ORCID 0000-0001-8956-9241
Akiyoshi HirayamaInstitute for Advanced Biosciences, Keio University, Yamagata, Japan.ORCID 0000-0002-0440-6820
Tomoyoshi SogaInstitute for Advanced Biosciences, Keio University, Yamagata, Japan.ORCID 0000-0001-9502-2509
James R EdwardsNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.
Zeynep KayaNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.ORCID 0000-0002-5626-262X
Charlotte PalmerNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.
Freddie C HamdyNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.ORCID 0000-0003-2627-2154
Claire M EdwardsNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.ORCID 0000-0002-1257-5659
University of Oxford · GBKeio University · JPNuffield Orthopaedic Centre · GB

Funding

Versus Arthritis 20631
6 · The paper itself

Abstract

The spread of cancer to bone is invariably fatal, with complex cross-talk between tumor cells and the bone microenvironment responsible for driving disease progression. By combining in silico analysis of patient datasets with metabolomic profiling of prostate cancer cells cultured with bone cells, we demonstrate the changing energy requirements of prostate cancer cells in the bone microenvironment, identifying the pentose phosphate pathway (PPP) as elevated in prostate cancer bone metastasis, with increased expression of the PPP rate-limiting enzyme glucose-6-phosphate dehydrogenase (G6PD) associated with a reduction in progression-free survival. Genetic and pharmacologic manipulation demonstrates that G6PD inhibition reduces prostate cancer growth and migration, associated with changes in cellular redox state and increased chemosensitivity. Genetic blockade of G6PD in vivo results in reduction of tumor growth within bone. In summary, we demonstrate the metabolic plasticity of prostate cancer cells in the bone microenvironment, identifying the PPP and G6PD as metabolic targets for the treatment of prostate cancer bone metastasis.

Indexed as

Glucosephosphate DehydrogenaseProstatic NeoplasmsCell Line, TumorHumansMaleMetabolomicsPentose Phosphate PathwayTumor MicroenvironmentG6PD protein, humanGlucosephosphate Dehydrogenase

Identifiers

PMID35213227
PMCPMC8880772
OpenAlexW4214704642

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.