Evidence map›Paper›PMID 27581357›Full record

ArticleBlood2016

inv(16) and NPM1mut AMLs engraft human cytokine knock-in mice.

Jana M Ellegast, Philipp J Rauch, Larisa V Kovtonyuk, Rouven Müller, Ulrich Wagner, Yasuyuki Saito, Nicole Wildner-Verhey van Wijk, Christine Fritz, Anahita Rafiei, Veronika Lysenko and 6 more

Abstract read
In one paragraph

Article in Blood, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

  1. Trial
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  11. Review
  12. Humanized mouse models for immuno-oncology research.Nature reviews. Clinical oncology · 2023
    Review
  13. Article
  14. Murine Models of Acute Myeloid Leukemia.Frontiers in oncology · 2022
    Review
  15. Article
  16. Article
  17. Review
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  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Jana M EllegastHematology, University Hospital and University of Zurich, Zurich, Switzerland.
Philipp J RauchHematology, University Hospital and University of Zurich, Zurich, Switzerland; Department of Medicine, Boston University School of Medicine, Boston, MA.
Larisa V KovtonyukHematology, University Hospital and University of Zurich, Zurich, Switzerland.
Rouven MüllerHematology, University Hospital and University of Zurich, Zurich, Switzerland.
Ulrich WagnerInstitute of Surgical Pathology, University Hospital of Zurich, Zurich, Switzerland.
Yasuyuki SaitoHematology, University Hospital and University of Zurich, Zurich, Switzerland; Division of Molecular and Cellular Signaling, Department of Biochemistry and Molecular Biology, Kobe University Graduate School of Medicine, Kobe, Japan; and.
Nicole Wildner-Verhey van WijkHematology, University Hospital and University of Zurich, Zurich, Switzerland.
Christine FritzInstitute of Surgical Pathology, University Hospital of Zurich, Zurich, Switzerland.
Anahita RafieiHematology, University Hospital and University of Zurich, Zurich, Switzerland.
Veronika LysenkoHematology, University Hospital and University of Zurich, Zurich, Switzerland.
Ewa DudkiewiczHematology, University Hospital and University of Zurich, Zurich, Switzerland.
Alexandre P TheocharidesHematology, University Hospital and University of Zurich, Zurich, Switzerland.
Davide SoldiniInstitute of Surgical Pathology, University Hospital of Zurich, Zurich, Switzerland.
Jeroen S GoedeHematology, University Hospital and University of Zurich, Zurich, Switzerland.
Richard A FlavellDepartment of Immunobiology and Howard Hughes Medical Institute, Yale University, New Haven, CT.
Markus G ManzHematology, University Hospital and University of Zurich, Zurich, Switzerland.

Funding

Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI DAVID L RIMM · 1985 to 2026
$85.0M
Understanding Hemotopoietic Neoplasias using Humanized MiceR01CA156689 · NCI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V, FLAVELL, RICHARD A · 2010 to 2014
$5.0M
NCI NIH HHS P30 CA016359NCI NIH HHS R01 CA156689
6 · The paper itself

Abstract

Favorable-risk human acute myeloid leukemia (AML) engrafts poorly in currently used immunodeficient mice, possibly because of insufficient environmental support of these leukemic entities. To address this limitation, we here transplanted primary human AML with isolated nucleophosmin (NPM1) mutation and AML with inv(16) in mice in which human versions of genes encoding cytokines important for myelopoiesis (macrophage colony-stimulating factor [M-CSF], interleukin-3, granulocyte-macrophage colony-stimulating factor, and thrombopoietin) were knocked into their respective mouse loci. NPM1

Indexed as

Disease Models, AnimalLeukemia, Myeloid, AcuteAnimalsChromosome AberrationsChromosomes, Human, Pair 16CytokinesGene Knock-In TechniquesHeterograftsHumansMiceMutationNeoplasm TransplantationNuclear ProteinsNucleophosminTransplantation, HeterologousCytokinesNPM1 protein, humanNpm1 protein, mouseNuclear ProteinsNucleophosmin

Identifiers

PMID27581357
PMCPMC5084606

What OpenQuestion holds

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Registered trials

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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.