Evidence map›Paper›PMID 27737961›Full record

ArticleGenes & development2016

Condensin II mutation causes T-cell lymphoma through tissue-specific genome instability.

Jessica Woodward, Gillian C Taylor, Dinesh C Soares, Shelagh Boyle, Daoud Sie, David Read, Keerthi Chathoth, Milica Vukovic, Nuria Tarrats, David Jamieson and 9 more

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
–field-weighted citation impact
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

35 citing papers in PubMed, 53 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Genome control by SMC complexes.Nature reviews. Molecular cell biology · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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

19 authors at 6 institutions in 2 countries.

Jessica WoodwardMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.
Gillian C TaylorMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.
Dinesh C SoaresMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.
Shelagh BoyleMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.
Daoud SieDepartment of Pathology, VU University Medical Center, 1007 MB Amsterdam, The Netherlands.
David ReadMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.
Keerthi ChathothMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.
Milica VukovicMRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh EH16 4UU, United Kingdom.
Nuria TarratsEdinburgh Cancer Research UK Centre, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.
David JamiesonNorthern Institute for Cancer Research, University of Newcastle upon Tyne, Newcastle upon Tyne NE2 4AD, United Kingdom.
Kirsteen J CampbellCancer Research UK Beatson Institute, Bearsden, Glasgow G61 1BD, United Kingdom.
Karen BlythCancer Research UK Beatson Institute, Bearsden, Glasgow G61 1BD, United Kingdom.
Juan Carlos AcostaEdinburgh Cancer Research UK Centre, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.
Bauke YlstraDepartment of Pathology, VU University Medical Center, 1007 MB Amsterdam, The Netherlands.
Mark J ArendsEdinburgh Cancer Research UK Centre, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.
Kamil R KrancMRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh EH16 4UU, United Kingdom.
Andrew P JacksonMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.
Wendy A BickmoreMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.
Andrew J WoodMRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, United Kingdom.ORCID http://orcid.org/0000-0002-0653-2070
Institute of Genetics and Cancer · GBEdinburgh Cancer Research · GBAmsterdam UMC Location Vrije Universiteit Amsterdam · NLCancer Research UK Scotland Institute · GBMRC Centre for Regenerative Medicine · GBNewcastle University · GB

Funding

Cancer Research UK 14633Cancer Research UK 16243Medical Research Council MC_PC_U127527202Medical Research Council MC_PC_U127580972Medical Research Council MR/K01563X/1Wellcome Trust
6 · The paper itself

Abstract

Chromosomal instability is a hallmark of cancer, but mitotic regulators are rarely mutated in tumors. Mutations in the condensin complexes, which restructure chromosomes to facilitate segregation during mitosis, are significantly enriched in cancer genomes, but experimental evidence implicating condensin dysfunction in tumorigenesis is lacking. We report that mice inheriting missense mutations in a condensin II subunit (Caph2

Indexed as

Adenosine TriphosphatasesAnaphaseAnimalsCells, CulturedChromosome StructuresDNA-Binding ProteinsFemaleGenomic InstabilityLymphoma, T-CellMaleMetaphaseMiceMultiprotein ComplexesMutation, MissenseThymocytesThymus NeoplasmsAdenosine Triphosphatasescondensin complexesDNA-Binding ProteinsMultiprotein Complexeschromosome structurecondensingenome instabilitylymphomamitosis

Identifiers

PMID27737961
PMCPMC5088566
OpenAlexW2529963138

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.