Evidence map›Paper›PMID 21030981›Full record

ArticleLeukemia2011

PHF6 mutations in adult acute myeloid leukemia.

P Van Vlierberghe, J Patel, O Abdel-Wahab, C Lobry, C V Hedvat, M Balbin, C Nicolas, A R Payer, H F Fernandez, M S Tallman and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Leukemia, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

95 citing papers in PubMed, 171 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Article
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  6. Article
  7. Beyond XX and XY, Understanding Sex Differences in Leukemia.Medical sciences (Basel, Switzerland) · 2026
    Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Late-onsetHaematologica · 2024
    Article
  15. Article
  16. Review
  17. Annals of laboratory medicine · 2024
    Article
  18. Article
  19. PHF6 suppresses self-renewal of leukemic stem cells in AML.bioRxiv : the preprint server for biology · 2024
    Article
  20. Article

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

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

18 authors at 10 institutions in 3 countries.

P Van VlierbergheInstitute for Cancer Genetics, Columbia University Medical Center, New York, NY 10032, USA.
J Patel
O Abdel-Wahab
C Lobry
C V Hedvat
M Balbin
C Nicolas
A R Payer
H F Fernandez
M S Tallman
E Paietta
A Melnick
P Vandenberghe
F Speleman
I Aifantis
J Cools
R Levine
A Ferrando
Memorial Sloan Kettering Cancer Center · USCancer Genetics (United States) · USHospital Universitario Central de Asturias · ESHoward Hughes Medical Institute · USKU Leuven · BECornell University · USGhent University Hospital · BEInstituto de Investigación Sanitaria del Principado de Asturias · ESMoffitt Cancer Center · USMontefiore Medical Center · US

Funding

Mechanisms of T-Cell Leukemogenesis Induced by Notch1R01CA120196 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI FERRANDO, ADOLFO A. · 2007 to 2011
$2.1M
Mechanisms of T cell leukemia induction and maintenanceR01CA149655 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AIFANTIS, IANNIS · 2010 to 2015
$2.0M
Genetic Dissection of Acute Myeloid Leukemia.R01CA169784 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI AIFANTIS, IANNIS, LEVINE, ROSS L · 2014 to 2018
$1.8M
The role of AKT signaling in NOTCH1 induced leukemiasR01CA129382 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI FERRANDO, ADOLFO A. · 2008 to 2012
$1.7M
The role of PHF6 in T-cell acute lymphoblastic leukemiaR01CA155743 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI FERRANDO, ADOLFO A. · 2011 to 2015
$1.6M
Howard Hughes Medical InstituteNCI NIH HHS R01 CA120196NCI NIH HHS R01CA120196NCI NIH HHS R01 CA129382NCI NIH HHS R01CA129382NCI NIH HHS R01 CA149655NCI NIH HHS R01 CA155743NCI NIH HHS R01 CA169784
6 · The paper itself

Abstract

Loss of function mutations and deletions encompassing the plant homeodomain finger 6 (PHF6) gene are present in about 20% of T-cell acute lymphoblastic leukemias (ALLs). Here, we report the identification of recurrent mutations in PHF6 in 10/353 adult acute myeloid leukemias (AMLs). Genetic lesions in PHF6 found in AMLs are frameshift and nonsense mutations distributed through the gene or point mutations involving the second plant homeodomain (PHD)-like domain of the protein. As in the case of T-ALL, where PHF6 alterations are found almost exclusively in males, mutations in PHF6 were seven times more prevalent in males than in females with AML. Overall, these results identify PHF6 as a tumor suppressor gene mutated in AML and extend the role of this X-linked tumor suppressor gene in the pathogenesis of hematologic tumors.

Indexed as

MutationAdultAgedAnimalsCarrier ProteinsFemaleGenes, Tumor SuppressorHematopoietic Stem CellsHumansLeukemia, Myeloid, AcuteMaleMiceMiddle AgedMyeloid CellsRepressor ProteinsSex CharacteristicsCarrier ProteinsPHF6 protein, humanRepressor Proteins

Identifiers

PMID21030981
PMCPMC3878659
OpenAlexW1996753824

What OpenQuestion holds

Textmetadata
LicenceTDM
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.