Evidence map›Paper›PMID 30049824›Full record

ArticleHaematologica2018

BCR-ABL1 mediated miR-150 downregulation through MYC contributed to myeloid differentiation block and drug resistance in chronic myeloid leukemia.

Klara Srutova, Nikola Curik, Pavel Burda, Filipp Savvulidi, Giovannino Silvestri, Rossana Trotta, Hana Klamova, Pavla Pecherkova, Zofie Sovova, Jitka Koblihova and 3 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

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  14. Emerging role of MYB transcription factors in cancer drug resistance.Cancer drug resistance (Alhambra, Calif.) · 2024
    Review
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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

13 authors at 3 institutions in 2 countries.

Klara SrutovaInstitute of Hematology and Blood Transfusion, Prague, Czech Republic.
Nikola CurikInstitute of Hematology and Blood Transfusion, Prague, Czech Republic.
Pavel BurdaInstitute of Hematology and Blood Transfusion, Prague, Czech Republic.
Filipp SavvulidiInstitute of Pathological Physiology, First Medical Faculty, Charles University, Prague, Czech Republic.
Giovannino SilvestriDepartment of Medicine, Marlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland Baltimore, MD, USA.
Rossana TrottaDepartment of Microbiology and Immunology, Marlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland Baltimore, MD, USA.
Hana KlamovaInstitute of Hematology and Blood Transfusion, Prague, Czech Republic.
Pavla PecherkovaInstitute of Hematology and Blood Transfusion, Prague, Czech Republic.
Zofie SovovaInstitute of Hematology and Blood Transfusion, Prague, Czech Republic.
Jitka KoblihovaInstitute of Hematology and Blood Transfusion, Prague, Czech Republic.
Tomas StopkaBIOCEV, First Medical Faculty, Charles University, Vestec, Czech Republic.
Danilo PerrottiDepartment of Medicine, Marlene and Stewart Greenebaum Comprehensive Cancer Center, University of Maryland Baltimore, MD, USA.
Katerina Machova PolakovaInstitute of Hematology and Blood Transfusion, Prague, Czech Republic katerina.machova@uhkt.cz.
Institute of Haematology and Blood Transfusion · CZCharles University · CZUniversity of Maryland, Baltimore · US

Funding

Role of microRNAs in the regulation of CML stem cell survival and self renewalR01CA163800 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI PERROTTI, DANILO · 2012 to 2017
$1.6M
NCI NIH HHS R01 CA163800
6 · The paper itself

Abstract

The fusion oncoprotein BCR-ABL1 exhibits aberrant tyrosine kinase activity and it has been proposed that it deregulates signaling networks involving both transcription factors and non-coding microRNAs that result in chronic myeloid leukemia (CML). Previously, microRNA expression profiling showed deregulated expression of miR-150 and miR-155 in CML. In this study, we placed these findings into the broader context of the MYC/miR-150/MYB/miR-155/PU.1 oncogenic network. We propose that up-regulated MYC and miR-155 in CD34

Indexed as

AdultAgedCell DifferentiationCell Line, TumorCell ProliferationDown-RegulationDrug Resistance, NeoplasmFemaleFusion Proteins, bcr-ablGene Expression Regulation, LeukemicGenes, mycHL-60 CellsHumansK562 CellsLeukemia, Myelogenous, Chronic, BCR-ABL PositiveMaleFusion Proteins, bcr-ablMicroRNAsMIR150, humanProtein Kinase Inhibitors

Identifiers

PMID30049824
PMCPMC6269310
OpenAlexW2885006465

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.