Evidence map›Paper›PMID 15674412›Full record

ArticleLeukemia2005

A new recurrent inversion, inv(7)(p15q34), leads to transcriptional activation of HOXA10 and HOXA11 in a subset of T-cell acute lymphoblastic leukemias.

F Speleman, B Cauwelier, N Dastugue, J Cools, B Verhasselt, B Poppe, N Van Roy, J Vandesompele, C Graux, A Uyttebroeck and 11 more

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In one paragraph

Article in Leukemia, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

50 citing papers in PubMed, 118 citations in OpenAlex.

  1. Review
  2. Article
  3. Acute lymphoblastic leukaemia.Nature reviews. Disease primers · 2024
    Review
  4. Review
  5. Article
  6. Article
  7. The Genetics and Mechanisms of T-Cell Acute Lymphoblastic Leukemia.Cold Spring Harbor perspectives in medicine · 2020
    Review
  8. A higher-order configuration of the heterodimeric DOT1L-AF10 coiled-coil domains potentiates their leukemogenenic activity.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Deregulation of the HOXA9/MEIS1 axis in acute leukemia.Current opinion in hematology · 2016
    Review
  14. Article
  15. Review
  16. Article
  17. Prognostification of ALL by Cytogenetics.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2015
    Review
  18. Article
  19. Oncology letters · 2014
    Article
  20. Genomic characterization of acute leukemias.Medical principles and practice : international journal of the Kuwait University, Health Science Centre · 2014
    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

21 authors at 3 institutions in 2 countries.

F SpelemanCentre for Medical Genetics, Ghent University Hospital, Ghent, Belgium. franki.speleman@ugent.be
B Cauwelier
N Dastugue
J Cools
B Verhasselt
B Poppe
N Van Roy
J Vandesompele
C Graux
A Uyttebroeck
M Boogaerts
B De Moerloose
Y Benoit
D Selleslag
J Billiet
A Robert
F Huguet
P Vandenberghe
A De Paepe
P Marynen
A Hagemeijer
Ghent University Hospital · BEKU Leuven · BEHôpital Purpan · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chromosomal translocations with breakpoints in T-cell receptor (TCR) genes are recurrent in T-cell malignancies. These translocations involve the TCRalphadelta gene (14q11), the TCRbeta gene (7q34) and to a lesser extent the TCRgamma gene at chromosomal band 7p14 and juxtapose T-cell oncogenes next to TCR regulatory sequences leading to deregulated expression of those oncogenes. Here, we describe a new recurrent chromosomal inversion of chromosome 7, inv(7)(p15q34), in a subset of patients with T-cell acute lymphoblastic leukemia characterized by CD2 negative and CD4 positive, CD8 negative blasts. This rearrangement juxtaposes the distal part of the HOXA gene cluster on 7p15 to the TCRbeta locus on 7q34. Real time quantitative PCR analysis for all HOXA genes revealed high levels of HOXA10 and HOXA11 expression in all inv(7) positive cases. This is the first report of a recurrent chromosome rearrangement targeting the HOXA gene cluster in T-cell malignancies resulting in deregulated HOXA gene expression (particularly HOXA10 and HOXA11) and is in keeping with a previous report suggesting HOXA deregulation in MLL-rearranged T- and B cell lymphoblastic leukemia as the key factor in leukaemic transformation. Finally, our observation also supports the previous suggested role of HOXA10 and HOXA11 in normal thymocyte development.

Indexed as

Chromosome InversionAdolescentAdultChildChild, PreschoolChromosomes, Human, Pair 7Cytogenetic AnalysisDNA-Binding ProteinsFemaleGene Expression Regulation, NeoplasticGene Rearrangement, T-LymphocyteHomeobox A10 ProteinsHomeodomain ProteinsHumansImmunophenotypingLeukemia-Lymphoma, Adult T-CellDNA-Binding ProteinsHomeobox A10 ProteinsHomeodomain ProteinsHOXA10 protein, humanHOXA11 protein, human

Identifiers

PMID15674412
OpenAlexW2088175344

What OpenQuestion holds

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Read underepoch 390

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.