Evidence map›Paper›PMID 27447965›Full record

ArticleOncotarget2016

MicroRNA fingerprints in juvenile myelomonocytic leukemia (JMML) identified miR-150-5p as a tumor suppressor and potential target for treatment.

Pier Paolo Leoncini, Alice Bertaina, Dimitrios Papaioannou, Christian Flotho, Riccardo Masetti, Silvia Bresolin, Giuseppe Menna, Nicola Santoro, Marco Zecca, Giuseppe Basso and 10 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Current Treatment of Juvenile Myelomonocytic Leukemia.Journal of clinical medicine · 2021
    Review
  9. Observational
  10. Article
  11. Article
  12. Observational
  13. Article
  14. [Advances in the treatment of juvenile myelomonocytic leukemia].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2018
    Review
  15. Article
  16. MiRNA Dysregulation in Childhood Hematological Cancer.International journal of molecular sciences · 2018
    Review
  17. MiR-150 Inhibits Cell Growth In Vitro and In Vivo by Restraining the RAB11A/WNT/β-Catenin Pathway in Thyroid Cancer.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  18. Article
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

20 authors at 10 institutions in 3 countries.

Pier Paolo LeonciniDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Bambino Gesù Children's Hospital, Rome, Italy.
Alice BertainaDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Bambino Gesù Children's Hospital, Rome, Italy.
Dimitrios PapaioannouDivision of Hematology, Arthur G. James Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.
Christian FlothoDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, University of Freiburg, Freiburg, Germany.
Riccardo MasettiDepartment of Pediatrics, "Lalla Seràgnoli" Hematology-Oncology Unit, University of Bologna, Bologna, Italy.
Silvia BresolinDepartment of Woman and Child Health, Haemato-Oncology Division, University of Padova, Azienda Ospedaliera di Padova, Padova, Italy.
Giuseppe MennaDepartment of Paediatric Haemato-Oncology, Santobono-Pausilipon Hospital, Napoli, Italy.
Nicola SantoroDepartment of Paediatrics, Paediatric Unit 'F. Vecchio', University of Bari, Bari, Italy.
Marco ZeccaDepartment of Paediatric Haematology and Oncology, Fondazione IRCCS Policlinico S. Matteo, University of Pavia, Pavia, Italy.
Giuseppe BassoDepartment of Woman and Child Health, Haemato-Oncology Division, University of Padova, Azienda Ospedaliera di Padova, Padova, Italy.
Giovanni NigitaDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH, USA.
Dario VenezianoDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH, USA.
Sara PagottoUnit of General Pathology, Center of Excellence on Aging and Translational Medicine (CeSI-MeT), G. d'Annunzio University, Chieti, Italy.
Katia D'OvidioDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Bambino Gesù Children's Hospital, Rome, Italy.
Rossella RotaDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Bambino Gesù Children's Hospital, Rome, Italy.
Adrienne DorranceDivision of Hematology, Arthur G. James Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.
Carlo M CroceDepartment of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH, USA.
Charlotte NiemeyerDepartment of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, University of Freiburg, Freiburg, Germany.
Franco LocatelliDepartment of Pediatric Hematology and Oncology, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Bambino Gesù Children's Hospital, Rome, Italy.
Ramiro GarzonDivision of Hematology, Arthur G. James Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.
Istituti di Ricovero e Cura a Carattere Scientifico · ITThe Ohio State University · USThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USAzienda Ospedaliera di Padova · ITUniversity of Chieti-Pescara · ITUniversity of Freiburg · DESantobono Children's Hospital · ITUniversity of Bari Aldo Moro · ITUniversity of Bologna · ITUniversity of Pavia · IT

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
Cancer Gene Discovery to Identify Targetable TargetsR35CA197706 · NCI · OHIO STATE UNIVERSITY · PI CROCE, CARLO M · 2015 to 2021
$6.4M
NCI NIH HHS P30 CA016058NCI NIH HHS R35 CA197706
6 · The paper itself

Abstract

Juvenile myelomonocytic leukemia (JMML) is an aggressive leukemia of early childhood characterized by aberrant proliferation of myelomonocytic cells and hypersensitivity to GM-CSF stimulation. Mutually exclusive mutations in the RAS/ERK pathway genes such as PTPN11, NRAS, KRAS, CBL, or NF1 are found in ~90% of the cases. These mutations give rise to disease at least in part by activating STAT5 through phosphorylation and by promoting cell growth. MicroRNAs (miRs) are small non-coding RNAs that regulate gene expression, which are often deregulated in leukemia. However, little is known about their role in JMML. Here, we report distinctive miR expression signatures associated with the molecular subgroups of JMML. Among the downregulated miRs in JMML, miR-150-5p was found to target STAT5b, a gene which is often over-activated in JMML, and contributes to the characteristic aberrant signaling of this disorder. Moreover, loss of miR-150-5p and upregulation of STAT5b expression were also identified in a murine model of JMML. Ectopic overexpression of miR-150-5p in mononuclear cells from three JMML patients significantly decreased cell proliferation. Altogether, our data indicate that miR expression is deregulated in JMML and may play a role in the pathogenesis of this disorder by modulating key effectors of cytokine receptor pathways.

Indexed as

AnimalsChildChild, PreschoolFemaleGene Expression Regulation, NeoplasticGenes, Tumor SuppressorGranulocyte-Macrophage Colony-Stimulating FactorHumansInfantInfant, NewbornLeukemia, Myelomonocytic, JuvenileMaleMiceMicroRNAsMutationSTAT5 Transcription FactorGranulocyte-Macrophage Colony-Stimulating FactorMicroRNAsMIR150, humanSTAT5B protein, humanSTAT5 Transcription FactorGM-CSFJMMLmicroRNAmiR-150STAT5b

Identifiers

PMID27447965
PMCPMC5342425
OpenAlexW2465069143

What OpenQuestion holds

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LicenceCC BY
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.