Evidence map›Paper›PMID 21160474›Full record

ArticleNature2011

Genetic variegation of clonal architecture and propagating cells in leukaemia.

Kristina Anderson, Christoph Lutz, Frederik W van Delft, Caroline M Bateman, Yanping Guo, Susan M Colman, Helena Kempski, Anthony V Moorman, Ian Titley, John Swansbury and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 437 papers.

0numbers the graph read from it
0cells of the map it votes in
437citing 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

437 citing papers in PubMed.

  1. Genomic Classification and Prognosis in Acute Myeloid Leukemia.The New England journal of medicine · 2016
    Trial
  2. Article
  3. Review
  4. Article
  5. Seq2Karyotype (S2K): A Method forbioRxiv : the preprint server for biology · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Resolving tumor evolution: a phylogenetic approach.Journal of the National Cancer Center · 2024
    Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Kristina AndersonSection of Haemato-Oncology, The Institute of Cancer Research, Sutton SM2 5NG, UK.
Christoph Lutz
Frederik W van Delft
Caroline M Bateman
Yanping Guo
Susan M Colman
Helena Kempski
Anthony V Moorman
Ian Titley
John Swansbury
Lyndal Kearney
Tariq Enver
Mel Greaves

Funding

Medical Research Council MC_U137973817
6 · The paper itself

Abstract

Little is known of the genetic architecture of cancer at the subclonal and single-cell level or in the cells responsible for cancer clone maintenance and propagation. Here we have examined this issue in childhood acute lymphoblastic leukaemia in which the ETV6-RUNX1 gene fusion is an early or initiating genetic lesion followed by a modest number of recurrent or 'driver' copy number alterations. By multiplexing fluorescence in situ hybridization probes for these mutations, up to eight genetic abnormalities can be detected in single cells, a genetic signature of subclones identified and a composite picture of subclonal architecture and putative ancestral trees assembled. Subclones in acute lymphoblastic leukaemia have variegated genetics and complex, nonlinear or branching evolutionary histories. Copy number alterations are independently and reiteratively acquired in subclones of individual patients, and in no preferential order. Clonal architecture is dynamic and is subject to change in the lead-up to a diagnosis and in relapse. Leukaemia propagating cells, assayed by serial transplantation in NOD/SCID IL2Rγ(null) mice, are also genetically variegated, mirroring subclonal patterns, and vary in competitive regenerative capacity in vivo. These data have implications for cancer genomics and for the targeted therapy of cancer.

Indexed as

AnimalsClone CellsCore Binding Factor Alpha 2 SubunitDisease ProgressionDNA Copy Number VariationsDNA Mutational AnalysisETS Translocation Variant 6 ProteinGenetic VariationGenotypeHumansImmunophenotypingIn Situ Hybridization, FluorescenceInterleukin Receptor Common gamma SubunitMiceMice, Inbred NODMice, SCIDCore Binding Factor Alpha 2 SubunitETS Translocation Variant 6 ProteinIl2rg protein, mouseInterleukin Receptor Common gamma SubunitOncogene Proteins, FusionTEL-AML1 fusion protein

Identifiers

PMID21160474

What OpenQuestion holds

Textmetadata
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.