Evidence map›Paper›PMID 17347684›Full record

ArticleThe Journal of clinical investigation2007

The homeobox gene CDX2 is aberrantly expressed in most cases of acute myeloid leukemia and promotes leukemogenesis.

Claudia Scholl, Dimple Bansal, Konstanze Döhner, Karina Eiwen, Brian J P Huntly, Benjamin H Lee, Frank G Rücker, Richard F Schlenk, Lars Bullinger, Hartmut Döhner and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
6.7field-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

64 citing papers in PubMed, 132 citations in OpenAlex.

  1. Review
  2. Regulation of HOX gene expression in AML.Blood cancer journal · 2024
    Review
  3. Aberrant stem cell and developmental programs in pediatric leukemia.Frontiers in cell and developmental biology · 2024
    Review
  4. Article
  5. Review
  6. Article
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  12. Neogenin-1 distinguishes between myeloid-biased and balancedProceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Survival regulation of leukemia stem cells.Cellular and molecular life sciences : CMLS · 2016
    Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 2 countries.

Claudia SchollDivision of Hematology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Dimple Bansal
Konstanze Döhner
Karina Eiwen
Brian J P Huntly
Benjamin H Lee
Frank G Rücker
Richard F Schlenk
Lars Bullinger
Hartmut Döhner
D Gary Gilliland
Stefan Fröhling
University Hospital Ulm · DEBrigham and Women's Hospital · USHarvard University · US

Funding

TYROSINE KINASE ONCOGENESIS IN MYELOID LEUKEMIAP01CA066996 · NCI · DANA-FARBER CANCER INSTITUTE · PI SCOTT A ARMSTRONG · 1996 to 2026
$52.5M
Systems Analysis of Cancer Pathways in Mouse ModelsU01CA105423 · NCI · DANA-FARBER CANCER INSTITUTE · PI ORKIN, STUART H · 2004 to 2013
$8.4M
Medical Research Council G116/187NCI NIH HHS CA105423NCI NIH HHS CA66996NCI NIH HHS P01 CA066996NCI NIH HHS U01 CA105423
6 · The paper itself

Abstract

The homeobox transcription factor CDX2 plays an important role in embryonic development and regulates the proliferation and differentiation of intestinal epithelial cells in the adult. We have found that CDX2 is expressed in leukemic cells of 90% of patients with acute myeloid leukemia (AML) but not in hematopoietic stem and progenitor cells derived from normal individuals. Stable knockdown of CDX2 expression by RNA interference inhibited the proliferation of various human AML cell lines and strongly reduced their clonogenic potential in vitro. Primary murine hematopoietic progenitor cells transduced with Cdx2 acquired serial replating activity, were able to be continuously propagated in liquid culture, generated fully penetrant and transplantable AML in BM transplant recipients, and displayed dysregulated expression of Hox family members in vitro and in vivo. These results demonstrate that aberrant expression of the developmental regulatory gene CDX2 in the adult hematopoietic compartment is a frequent event in the pathogenesis of AML; suggest a role for CDX2 as part of a common effector pathway that promotes the proliferative capacity and self-renewal potential of myeloid progenitor cells; and support the hypothesis that CDX2 is responsible, in part, for the altered HOX gene expression that is observed in most cases of AML.

Indexed as

Gene Expression Regulation, NeoplasticGenes, HomeoboxBone Marrow TransplantationCDX2 Transcription FactorChromosome MappingChromosomes, HumanHomeodomain ProteinsHumansKaryotypingLeukemia, Myeloid, AcuteRNA InterferenceTranslocation, GeneticCDX2 protein, humanCDX2 Transcription FactorHomeodomain Proteins

Identifiers

PMID17347684
PMCPMC1810574
OpenAlexW1965243787

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.