Evidence map›Paper›PMID 33569005›Full record

ArticleFrontiers in pharmacology2020

miRNome profiling of LSC-enriched CD34

María Sol Ruiz, María Belén Sánchez, Simone Bonecker, Carolina Furtado, Daniel Koile, Patricio Yankilevich, Santiago Cranco, María Del Rosario Custidiano, Josefina Freitas, Beatriz Moiraghi and 10 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. 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

20 authors at 9 institutions in 3 countries.

María Sol RuizCentro de Investigaciones Oncológicas-Fundación Cáncer, Ciudad Autónoma de Buenos Aires, Argentina.
María Belén SánchezCentro de Investigaciones Oncológicas-Fundación Cáncer, Ciudad Autónoma de Buenos Aires, Argentina.
Simone BoneckerCentro de Transplante de Medula Óssea, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.
Carolina FurtadoPrograma de Genética, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.
Daniel KoileInstituto de Investigación en Biomedicina de Buenos Aires (IBioBA)-CONICET-Partner Institute of the Max Planck Society, Ciudad Autónoma de Buenos Aires, Argentina.
Patricio YankilevichInstituto de Investigación en Biomedicina de Buenos Aires (IBioBA)-CONICET-Partner Institute of the Max Planck Society, Ciudad Autónoma de Buenos Aires, Argentina.
Santiago CrancoInstituto Alexander Fleming, Ciudad Autónoma de Buenos Aires, Argentina.
María Del Rosario CustidianoInstituto Alexander Fleming, Ciudad Autónoma de Buenos Aires, Argentina.
Josefina FreitasHospital Nacional Posadas, Buenos Aires, Argentina.
Beatriz MoiraghiHospital J. M. Ramos Mejía, Ciudad Autónoma de Buenos Aires, Argentina.
Mariel Ana PérezHospital Interzonal General de Agudos, Buenos Aires, Argentina.
Carolina PavlovskyFundaleu, Ciudad Autónoma de Buenos Aires, Argentina.
Ana Inés VarelaHospital J. M. Ramos Mejía, Ciudad Autónoma de Buenos Aires, Argentina.
Verónica VentrigliaHospital Nacional Posadas, Buenos Aires, Argentina.
Julio César Sánchez ÁvalosInstituto Alexander Fleming, Ciudad Autónoma de Buenos Aires, Argentina.
Irene LarripaInstituto de Medicina Experimental, CONICET/Academia Nacional de Medicina, Ciudad Autónoma de Buenos Aires, Argentina.
Ilana ZalcbergCentro de Transplante de Medula Óssea, Instituto Nacional de Câncer, Rio de Janeiro, Brazil.
José MordohCentro de Investigaciones Oncológicas, Fundación Cáncer, Buenos, Aires, Argentina.
Peter ValentDivision of Hematology and Hemostaseology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria.
Michele BianchiniCentro de Investigaciones Oncológicas-Fundación Cáncer, Ciudad Autónoma de Buenos Aires, Argentina.
Fundación para la Investigación, Docencia y Prevención del Cáncer · ARInstituto Alexander Fleming · ARInstituto Nacional do Câncer · BRBiomedicine Research Institute of Buenos Aires - CONICET - Partner Institute of the Max Planck Society · ARHospital Posadas · ARHospital Ramos Mejía · ARConsejo Nacional de Investigaciones Científicas y Técnicas · ARFundación Instituto Leloir · ARMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic myeloid leukemia (CML) is a myeloid stem cell neoplasm characterized by an expansion of myeloid progenitor cells and the presence of BCR-ABL1 oncoprotein. Since the introduction of specific BCR-ABL1 tyrosine kinase inhibitors (TKI), overall survival has improved significantly. However, under long-term therapy patients may have residual disease that originates from TKI-resistant leukemic stem cells (LSC). In this work, we analyzed the miRNome of LSC-enriched CD34

Indexed as

CD26leukemialeukemic stem cellmetabolismmicroRNAs

Identifiers

PMID33569005
PMCPMC7869017
OpenAlexW3124262013

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.