Evidence map›Paper›PMID 25686674›Full record

ReviewCancer genetics2015

The pathological role and prognostic impact of miR-181 in acute myeloid leukemia.

Hengyou Weng, Kumar Lal, Frank F Yang, Jianjun Chen

Open access · greenAbstract readReview
In one paragraph

Review in Cancer genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

44 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Constitutive systemic inflammation in Shwachman-Diamond Syndrome.Molecular medicine (Cambridge, Mass.) · 2025
    Article
  3. Article
  4. RNA mGenes & diseases · 2024
    Article
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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

4 authors at 3 institutions in 1 country.

Hengyou WengSection of Hematology/Oncology, Department of Medicine, University of Chicago, Chicago, IL, USA.
Kumar LalBiological Sciences Collegiate Division, University of Chicago, Chicago, IL, USA; Rush Medical College, Rush University Medical Center, Chicago, IL, USA.
Frank F YangBiological Sciences Collegiate Division, University of Chicago, Chicago, IL, USA; School of Medicine, Stanford University, Stanford, CA, USA.
Jianjun ChenSection of Hematology/Oncology, Department of Medicine, University of Chicago, Chicago, IL, USA. Electronic address: jchen@bsd.uchicago.edu.
University of Chicago · USRush University Medical Center · USStanford University · US

Funding

Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
Potential therapeutic implications of targeting miR-150 in acute myeloid leukemiaR01CA182528 · NCI · UNIVERSITY OF CINCINNATI · PI CHEN, JIANJUN · 2014 to 2018
$1.7M
The role and functional mechanism of TET1 in MLL-rearranged leukemiaR01CA178454 · NCI · UNIVERSITY OF CINCINNATI · PI CHEN, JIANJUN · 2014 to 2018
$1.7M
The role and functional mechanism of a miRNA cluster, mir-17-92 in leukemogenesisR01CA127277 · NCI · UNIVERSITY OF CHICAGO · PI CHEN, JIANJUN · 2008 to 2012
$1.4M
NCATS NIH HHS UL1 TR000430NCI NIH HHS R01 CA127277NCI NIH HHS R01CA127277NCI NIH HHS R01 CA178454NCI NIH HHS R01CA178454NCI NIH HHS R01 CA182528NCI NIH HHS R01CA182528
6 · The paper itself

Abstract

In addition to genetic abnormalities, such as chromosomal translocations and somatic mutations that have been widely acknowledged in the leukemogenesis of acute myeloid leukemia (AML), epigenetic modifications also play a vital role in this process. MicroRNA (miRNA) regulation is emerging as a new layer of epigenetic regulation besides DNA methylation and histone modifications. Among the miRNAs first identified to be specifically expressed in hematopoietic cells, the miR-181 family has been implicated in regulating the differentiation of B cells, T cells, and natural killer cells during normal hematopoiesis, and has been linked tightly to the pathogenesis and prognosis of AML. Accumulating evidence indicates that miR-181 acts as a tumor suppressor in the pathogenesis of AML and exhibits a significant impact on the survival of patients with AML. Herein, we review the role of miR-181 as a diagnostic marker and prognostic predictor in AML, and discuss the potential use of miR-181 as a therapeutic target for AML.

Indexed as

Biomarkers, TumorEpigenesis, GeneticGenes, Tumor SuppressorHematopoiesisHumansLeukemia, Myeloid, AcuteMicroRNAsPrognosisBiomarkers, TumorMicroRNAsMIrn181 microRNA, humanAcute myeloid leukemiadiagnostic markermiR-181prognostic predictortumor suppressor

Identifiers

PMID25686674
PMCPMC4466067
OpenAlexW2025826318

What OpenQuestion holds

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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.