Evidence map›Paper›PMID 17039236›Full record

ArticleLeukemia2007

Clinical, cytogenetic and molecular characteristics of 14 T-ALL patients carrying the TCRbeta-HOXA rearrangement: a study of the Groupe Francophone de Cytogénétique Hématologique.

B Cauwelier, H Cavé, C Gervais, M Lessard, C Barin, C Perot, J Van den Akker, F Mugneret, C Charrin, M P Pagès and 31 more

Abstract read
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In one paragraph

Article in Leukemia, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.2field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Review
  3. MonoallelicFrontiers in immunology · 2022
    Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. T-cell Acute Lymphoblastic Leukemia with del (7) (q11.2q22) and Aberrant Expression of Myeloid Markers.International journal of hematology-oncology and stem cell research · 2013
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. 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

41 authors at 18 institutions in 2 countries.

B CauwelierCentre for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
H Cavé
C Gervais
M Lessard
C Barin
C Perot
J Van den Akker
F Mugneret
C Charrin
M P Pagès
M-J Grégoire
P Jonveaux
M Lafage-Pochitaloff
M J Mozzicconacci
C Terré
I Luquet
P Cornillet-Lefebvre
B Laurence
G Plessis
C Lefebvre
D Leroux
H Antoine-Poirel
C Graux
L Mauvieux
P Heimann
C Chalas
E Clappier
B Verhasselt
Y Benoit
B D Moerloose
B Poppe
N Van Roy
K D Keersmaecker
J Cools
F Sigaux
J Soulier
A Hagemeijer
A D Paepe
N Dastugue
R Berger
F Speleman
Ghent University Hospital · BEInserm · FRCentre Hospitalier Régional et Universitaire de Nancy · FRCentre Hospitalier Universitaire de Reims · FRCentre Hospitalier Universitaire de Tours · FRHôpital Edouard Herriot · FRInstitut Paoli-Calmettes · FRLaboratoire de Biologie Structurale de la Cellule · FRSorbonne Université · FRVlaams Instituut voor Biotechnologie · BECentre Hospitalier de Versailles · FRCHU Dijon Bourgogne · FRErasmus Hospital · BEHôpital Georges-Clemenceau · FRHôpital Necker-Enfants Malades · FRHôpital Purpan · FRHôpital Robert-Debré · FRKU Leuven · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, we and others described a new chromosomal rearrangement, that is, inv(7)(p15q34) and t(7;7)(p15;q34) involving the T-cell receptor beta (TCRbeta) (7q34) and the HOXA gene locus (7p15) in 5% of T-cell acute lymphoblastic leukemia (T-ALL) patients leading to transcriptional activation of especially HOXA10. To further address the clinical, immunophenotypical and molecular genetic findings of this chromosomal aberration, we studied 330 additional T-ALLs. This revealed TCRbeta-HOXA rearrangements in five additional patients, which brings the total to 14 cases in 424 patients (3.3%). Real-time quantitative PCR analysis for HOXA10 gene expression was performed in 170 T-ALL patients and detected HOXA10 overexpression in 25.2% of cases including all the cases with a TCRbeta-HOXA rearrangement (8.2%). In contrast, expression of the short HOXA10 transcript, HOXA10b, was almost exclusively found in the TCRbeta-HOXA rearranged cases, suggesting a specific role for the HOXA10b short transcript in TCRbeta-HOXA-mediated oncogenesis. Other molecular and/or cytogenetic aberrations frequently found in subtypes of T-ALL (SIL-TAL1, CALM-AF10, HOX11, HOX11L2) were not detected in the TCRbeta-HOXA rearranged cases except for deletion 9p21 and NOTCH1 activating mutations, which were present in 64 and 67%, respectively. In conclusion, this study defines TCRbeta-HOXA rearranged T-ALLs as a distinct cytogenetic subgroup by clinical, immunophenotypical and molecular genetic characteristics.

Indexed as

AdolescentAdultChildChromosome DeletionChromosome InversionFemaleGene Rearrangement, T-LymphocyteHomeobox A10 ProteinsHomeodomain ProteinsHumansImmunophenotypingLeukemia-Lymphoma, Adult T-CellMaleMiddle AgedReceptor, Notch1Receptors, Antigen, T-Cell, alpha-betaHomeobox A10 ProteinsHomeodomain ProteinsHOXA10 protein, humanNOTCH1 protein, humanReceptor, Notch1Receptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID17039236
OpenAlexW1996088639

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.