Evidence map›Paper›PMID 20889924›Full record

ArticleBlood2010

C/EBPα regulated microRNA-34a targets E2F3 during granulopoiesis and is down-regulated in AML with CEBPA mutations.

John A Pulikkan, Philomina S Peramangalam, Viola Dengler, Phoenix A Ho, Claude Preudhomme, Soheil Meshinchi, Maximilian Christopeit, Oliver Nibourel, Carsten Müller-Tidow, Stefan K Bohlander and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 1 pooled it
4.6field-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

77 citing papers in PubMed, 1 synthesis or guideline pooled it, 124 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. MicroRNA-34a: the bad guy in age-related vascular diseases.Cellular and molecular life sciences : CMLS · 2021
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

17 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

12 authors at 6 institutions in 4 countries.

John A PulikkanDepartment of Internal Medicine IV-Oncology and Hematology, Martin Luther University Halle-Wittenberg, Halle, Germany
Philomina S Peramangalam
Viola Dengler
Phoenix A Ho
Claude Preudhomme
Soheil Meshinchi
Maximilian Christopeit
Oliver Nibourel
Carsten Müller-Tidow
Stefan K Bohlander
Daniel G Tenen
Gerhard Behre
Martin Luther University Halle-Wittenberg · DEFred Hutch Cancer Center · USUniversité de Lille · FRHarvard Stem Cell Institute · USHelmholtz Zentrum München · DEUniversity of Münster · DE

Funding

COG FOREIGN ACCRUALU10CA098543 · NCI · NATIONAL CHILDHOOD CANCER FOUNDATION · PI ADAMSON, PETER C. · 2003 to 2013
$335.5M
Children's Oncology Group Statistics &Data Center GrantU10CA098413 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI DEVIDAS, MEENAKSHI · 2003 to 2013
$67.5M
ROLE OF C/EBPalpha AND MYELOPOIESISR01HL056745 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI TENEN, DANIEL G · 1996 to 2010
$3.7M
NCI NIH HHS U10 CA098413NCI NIH HHS U10 CA098543NCI NIH HHS U10 CA98413NCI NIH HHS U10 CA98543NHLBI NIH HHS R01 HL056745NHLBI NIH HHS R01 HL56745
6 · The paper itself

Abstract

The transcription factor, CCAAT enhancer binding protein alpha (C/EBPα), is crucial for granulopoiesis and is deregulated by various mechanisms in acute myeloid leukemia (AML). Mutations in the CEBPA gene are reported in 10% of human patients with AML. Even though the C/EBPα mutants are known to display distinct biologic function during leukemogenesis, the molecular basis for this subtype of AML remains elusive. We have recently showed the significance of deregulation of C/EBPα-regulated microRNA (miR) in AML. In this study, we report that miR-34a is a novel target of C/EBPα in granulopoiesis. During granulopoiesis, miR-34a targets E2F3 and blocks myeloid cell proliferation. Analysis of AML samples with CEBPA mutations revealed a lower expression of miR-34a and elevated levels of E2F3 as well as E2F1, a transcriptional target of E2F3. Manipulation of miR-34a reprograms granulocytic differentiation of AML blast cells with CEBPA mutations. These results define miR-34a as a novel therapeutic target in AML with CEBPA mutations.

Indexed as

LeukopoiesisBlotting, WesternCCAAT-Enhancer-Binding ProteinsCell CycleCell DifferentiationChromatin ImmunoprecipitationE2F1 Transcription FactorE2F3 Transcription FactorFlow CytometryGene Expression Regulation, NeoplasticGranulocytesHematopoietic Stem CellsHumansLeukemia, Myeloid, AcuteLuciferasesMicroRNAsCCAAT-Enhancer-Binding ProteinsCEBPA protein, humanE2F1 protein, humanE2F1 Transcription FactorE2F3 protein, humanE2F3 Transcription FactorLuciferasesMicroRNAsMIRN34 microRNA, humanRNA, Messenger

Identifiers

PMID20889924
PMCPMC3031410
OpenAlexW1964118535

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.