Evidence map›Paper›PMID 29720585›Full record

ArticleNature communications2018

De novo activating mutations drive clonal evolution and enhance clonal fitness in KMT2A-rearranged leukemia.

Axel Hyrenius-Wittsten, Mattias Pilheden, Helena Sturesson, Jenny Hansson, Michael P Walsh, Guangchun Song, Julhash U Kazi, Jian Liu, Ramprasad Ramakrishan, Cristian Garcia-Ruiz and 12 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

30 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. CharacterizingCancers · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. International journal of molecular sciences · 2024
    Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  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

22 authors at 2 institutions in 2 countries.

Axel Hyrenius-WittstenDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, 221 84, Lund, Sweden.ORCID http://orcid.org/0000-0002-1239-4954
Mattias PilhedenDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, 221 84, Lund, Sweden.
Helena SturessonDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, 221 84, Lund, Sweden.
Jenny HanssonDivision of Molecular Hematology, Department of Laboratory Medicine, Lund University, 221 84, Lund, Sweden.ORCID http://orcid.org/0000-0001-9174-8089
Michael P WalshDepartment of Pathology, St. Jude Children´s Research Hospital, Memphis, TN, 38105, USA.
Guangchun SongDepartment of Pathology, St. Jude Children´s Research Hospital, Memphis, TN, 38105, USA.
Julhash U KaziDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, 223 63, Lund, Sweden.ORCID http://orcid.org/0000-0002-0719-5336
Jian LiuDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, 221 84, Lund, Sweden.
Ramprasad RamakrishanDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, 221 84, Lund, Sweden.
Cristian Garcia-RuizDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, 221 84, Lund, Sweden.
Stephanie NanceDepartment of Oncology, St. Jude Children´s Research Hospital, Memphis, TN, 38105, USA.
Pankaj GuptaDepartment of Computational Biology, St. Jude Children´s Research Hospital, Memphis, TN, 38105, USA.
Jinghui ZhangDepartment of Computational Biology, St. Jude Children´s Research Hospital, Memphis, TN, 38105, USA.
Lars RönnstrandDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, 223 63, Lund, Sweden.ORCID http://orcid.org/0000-0003-1275-5809
Anne HultquistDepartment of Pathology, Skane University Hospital, Lund University, 221 85, Lund, Sweden.
James R DowningDepartment of Pathology, St. Jude Children´s Research Hospital, Memphis, TN, 38105, USA.
Karin Lindkvist-PeterssonMedical Structural Biology, Department of Experimental Medical Science, 221 84 Lund University, Lund, Sweden.ORCID http://orcid.org/0000-0002-5209-3160
Kajsa PaulssonDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, 221 84, Lund, Sweden.ORCID http://orcid.org/0000-0001-7950-222X
Marcus JäråsDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, 221 84, Lund, Sweden.
Tanja A GruberDepartment of Pathology, St. Jude Children´s Research Hospital, Memphis, TN, 38105, USA.
Jing MaDepartment of Pathology, St. Jude Children´s Research Hospital, Memphis, TN, 38105, USA.
Anna K Hagström-AnderssonDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, 221 84, Lund, Sweden. Anna.Hagstrom@med.lu.se.ORCID http://orcid.org/0000-0002-2904-1311
Lund University · SESt. Jude Children's Research Hospital · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
NCI NIH HHS P30 CA021765
6 · The paper itself

Abstract

Activating signaling mutations are common in acute leukemia with KMT2A (previously MLL) rearrangements (KMT2A-R). These mutations are often subclonal and their biological impact remains unclear. Using a retroviral acute myeloid mouse leukemia model, we demonstrate that FLT3

Indexed as

Clonal EvolutionGene RearrangementMutationAcute DiseaseAnimalsCell Line, TumorCells, CulturedGene Expression Regulation, LeukemicHistone-Lysine N-MethyltransferaseLeukemia, MyeloidMice, Inbred C57BLMice, TransgenicMyeloid-Lymphoid Leukemia ProteinOncogene Proteins, FusionProto-Oncogene Proteins p21(ras)Histone-Lysine N-MethyltransferaseHras protein, mouseKmt2a protein, mouseMyeloid-Lymphoid Leukemia ProteinOncogene Proteins, FusionProto-Oncogene Proteins p21(ras)

Identifiers

PMID29720585
PMCPMC5932012
OpenAlexW2800596816

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.