Evidence map›Paper›PMID 25231743›Full record

ArticleLeukemia2015

MicroRNA-193b-3p acts as a tumor suppressor by targeting the MYB oncogene in T-cell acute lymphoblastic leukemia.

E Mets, J Van der Meulen, G Van Peer, M Boice, P Mestdagh, I Van de Walle, T Lammens, S Goossens, B De Moerloose, Y Benoit and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Leukemia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

62 citing papers in PubMed, 110 citations in OpenAlex.

  1. Review
  2. microRNA Profile of High-Grade B-Cell Lymphoma with 11q Aberration.International journal of molecular sciences · 2024
    Article
  3. HemaSphere · 2024
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. MicroRNAs and Heat Shock Proteins in Breast Cancer Biology.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Non-Coding RNAs in Hereditary Kidney Disorders.International journal of molecular sciences · 2021
    Review
  20. Article

2 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

20 authors at 4 institutions in 3 countries.

E MetsCenter for Medical Genetics, Ghent University, Ghent, Belgium.
J Van der MeulenCenter for Medical Genetics, Ghent University, Ghent, Belgium.
G Van PeerCenter for Medical Genetics, Ghent University, Ghent, Belgium.
M BoiceCancer Biology and Genetics, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
P MestdaghCenter for Medical Genetics, Ghent University, Ghent, Belgium.
I Van de WalleDepartment of Clinical Chemistry, Microbiology and Immunology, Ghent University Hospital, Ghent, Belgium.
T LammensDepartment of Pediatric Hematology-Oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent, Belgium.
S GoossensVIB/Department for Molecular Biomedical Research, Ghent University, Ghent, Belgium.
B De MoerlooseDepartment of Pediatric Hematology-Oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent, Belgium.
Y BenoitDepartment of Pediatric Hematology-Oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent, Belgium.
N Van RoyCenter for Medical Genetics, Ghent University, Ghent, Belgium.
E ClappierGenome Rearrangements and Cancer Laboratory, U462 INSERM, Laboratoire Central d'Hématologie and Institut Universitaire d'Hématologie, Hôpital Saint-Louis, Paris, France.
B PoppeCenter for Medical Genetics, Ghent University, Ghent, Belgium.
J VandesompeleCenter for Medical Genetics, Ghent University, Ghent, Belgium.
H-G WendelCancer Biology and Genetics, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
T TaghonDepartment of Clinical Chemistry, Microbiology and Immunology, Ghent University Hospital, Ghent, Belgium.
P RondouCenter for Medical Genetics, Ghent University, Ghent, Belgium.
J SoulierGenome Rearrangements and Cancer Laboratory, U462 INSERM, Laboratoire Central d'Hématologie and Institut Universitaire d'Hématologie, Hôpital Saint-Louis, Paris, France.
P Van VlierbergheCenter for Medical Genetics, Ghent University, Ghent, Belgium.
F SpelemanCenter for Medical Genetics, Ghent University, Ghent, Belgium.
Ghent University · BEGhent University Hospital · BEInserm · FRMemorial Sloan Kettering Cancer Center · US

Funding

Using mouse models to probe the relationship of oncogenesis to development and oU01CA105492 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI HOLLAND, ERIC C. · 2004 to 2013
$5.8M
Towards The Chemotherapy-Free Treatment of Follicular LymphomaR01CA183876 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI WENDEL, HANS-GUIDO · 2014 to 2018
$2.5M
The contribution of protein translation to tumorigenesisR01CA142798 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI WENDEL, HANS-GUIDO · 2010 to 2014
$1.9M
NCI NIH HHS R01 CA142798NCI NIH HHS R01-CA142798-01NCI NIH HHS R01 CA183876NCI NIH HHS U01 CA105492NCI NIH HHS U01CA105492-08
6 · The paper itself

Abstract

The MYB oncogene is a leucine zipper transcription factor essential for normal and malignant hematopoiesis. In T-cell acute lymphoblastic leukemia (T-ALL), elevated MYB levels can arise directly through T-cell receptor-mediated MYB translocations, genomic MYB duplications or enhanced TAL1 complex binding at the MYB locus or indirectly through the TAL1/miR-223/FBXW7 regulatory axis. In this study, we used an unbiased MYB 3'untranslated region-microRNA (miRNA) library screen and identified 33 putative MYB-targeting miRNAs. Subsequently, transcriptome data from two independent T-ALL cohorts and different subsets of normal T-cells were used to select miRNAs with relevance in the context of normal and malignant T-cell transformation. Hereby, miR-193b-3p was identified as a novel bona fide tumor-suppressor miRNA that targets MYB during malignant T-cell transformation thereby offering an entry point for efficient MYB targeting-oriented therapies for human T-ALL.

Indexed as

Gene Expression Regulation, Leukemic3' Untranslated RegionsAnimalsBasic Helix-Loop-Helix ProteinsCell Cycle ProteinsCell Transformation, NeoplasticF-Box ProteinsF-Box-WD Repeat-Containing Protein 7Gene Expression ProfilingGenomic LibraryHumansMiceMicroRNAsPrecursor T-Cell Lymphoblastic Leukemia-LymphomaPrimary Cell CultureProto-Oncogene Proteins3' Untranslated RegionsBasic Helix-Loop-Helix ProteinsCell Cycle ProteinsF-Box ProteinsF-Box-WD Repeat-Containing Protein 7FBXW7 protein, humanMicroRNAsMIR223, humanMIRN193 microRNA, humanProto-Oncogene ProteinsProto-Oncogene Proteins c-mybTAL1 protein, humanT-Cell Acute Lymphocytic Leukemia Protein 1Ubiquitin-Protein Ligases

Identifiers

PMID25231743
PMCPMC4890642
OpenAlexW2016818600

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.