Evidence map›Paper›PMID 32251294›Full record

ArticleNature communications2020

Low rates of mutation in clinical grade human pluripotent stem cells under different culture conditions.

Oliver Thompson, Ferdinand von Meyenn, Zoe Hewitt, John Alexander, Andrew Wood, Richard Weightman, Sian Gregory, Felix Krueger, Simon Andrews, Ivana Barbaric and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
6.9field-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

79 citing papers in PubMed, 136 citations in OpenAlex.

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  14. Unveiling genomic rearrangements in engineered iPSC lines by optical genome mapping.Molecular therapy. Methods & clinical development · 2025
    Article
  15. Genes · 2025
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  17. Review
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19 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

17 authors at 5 institutions in 3 countries.

Oliver ThompsonThe Centre for Stem Cell Biology, Department of Biomedical Science, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.
Ferdinand von MeyennEpigenetics Programme, Babraham Institute, Cambridge, CB22 3AT, UK.ORCID http://orcid.org/0000-0001-9920-3075
Zoe HewittThe Centre for Stem Cell Biology, Department of Biomedical Science, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.ORCID http://orcid.org/0000-0001-7519-7029
John AlexanderThe Centre for Stem Cell Biology, Department of Biomedical Science, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.ORCID http://orcid.org/0000-0003-3973-6501
Andrew WoodThe Centre for Stem Cell Biology, Department of Biomedical Science, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.ORCID http://orcid.org/0000-0002-5973-2092
Richard WeightmanThe Centre for Stem Cell Biology, Department of Biomedical Science, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.ORCID http://orcid.org/0000-0002-2593-8631
Sian GregoryThe Centre for Stem Cell Biology, Department of Biomedical Science, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.ORCID http://orcid.org/0000-0002-3014-2603
Felix KruegerBioinformatics Group, Babraham Institute, Cambridge, CB22 3AT, UK.ORCID http://orcid.org/0000-0002-5513-3324
Simon AndrewsBioinformatics Group, Babraham Institute, Cambridge, CB22 3AT, UK.
Ivana BarbaricThe Centre for Stem Cell Biology, Department of Biomedical Science, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.
Paul J GokhaleThe Centre for Stem Cell Biology, Department of Biomedical Science, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.ORCID http://orcid.org/0000-0001-7225-4403
Harry D MooreThe Centre for Stem Cell Biology, Department of Biomedical Science, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.
Wolf ReikEpigenetics Programme, Babraham Institute, Cambridge, CB22 3AT, UK.
Marta MiloThe Centre for Stem Cell Biology, Department of Biomedical Science, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK.ORCID http://orcid.org/0000-0002-6996-6431
Serena Nik-ZainalWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SA, UK.ORCID http://orcid.org/0000-0001-5054-1727
Kosuke YusaWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SA, UK. k.yusa@infront.kyoto-u.ac.jp.ORCID http://orcid.org/0000-0002-3442-021X
Peter W AndrewsThe Centre for Stem Cell Biology, Department of Biomedical Science, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK. p.w.andrews@sheffield.ac.uk.ORCID http://orcid.org/0000-0001-7215-4410
University of Sheffield · GBBabraham Institute · GBCambridge University Hospitals NHS Foundation Trust · GBInstitute of Cancer Research · GBKyoto University · JP

Funding

Cancer Research UK 22932Cancer Research UK 23433Cancer Research UK 23916Cancer Research UK 27815Cancer Research UK A23916Medical Research Council MR/L012537/1Wellcome Trust 206194Wellcome Trust WT206194
6 · The paper itself

Abstract

The occurrence of repetitive genomic changes that provide a selective growth advantage in pluripotent stem cells is of concern for their clinical application. However, the effect of different culture conditions on the underlying mutation rate is unknown. Here we show that the mutation rate in two human embryonic stem cell lines derived and banked for clinical application is low and not substantially affected by culture with Rho Kinase inhibitor, commonly used in their routine maintenance. However, the mutation rate is reduced by >50% in cells cultured under 5% oxygen, when we also found alterations in imprint methylation and reversible DNA hypomethylation. Mutations are evenly distributed across the chromosomes, except for a slight increase on the X-chromosome, and an elevation in intergenic regions suggesting that chromatin structure may affect mutation rate. Overall the results suggest that pluripotent stem cells are not subject to unusually high rates of genetic or epigenetic alterations.

Indexed as

Mutation RateCell Culture TechniquesCell LineChromosomes, Human, XCulture MediaDNA, IntergenicDNA MethylationDNA Mutational AnalysisEpigenesis, GeneticHumansOxidative StressOxygenPluripotent Stem CellsSequence Analysis, RNAWhole Genome SequencingCulture MediaDNA, IntergenicOxygen

Identifiers

PMID32251294
PMCPMC7089967
OpenAlexW3012580414

What OpenQuestion holds

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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.