Evidence map›Paper›PMID 32107471›Full record

ArticleLeukemia2020

miR-146a rs2431697 identifies myeloproliferative neoplasm patients with higher secondary myelofibrosis progression risk.

F Ferrer-Marín, A B Arroyo, B Bellosillo, E J Cuenca, L Zamora, J M Hernández-Rivas, J C Hernández-Boluda, C Fernandez-Rodriguez, E Luño, C García Hernandez and 19 more

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PubMed Publisher
In one paragraph

Article in Leukemia, 2020. 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
2.3field-weighted citation impact, top 11% 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, 22 citations in OpenAlex.

  1. Trial
  2. miR-146a mimic therapy protects against platelet-mediated thrombosis.Molecular therapy : the journal of the American Society of Gene Therapy · 2026
    Article
  3. Review
  4. Article
  5. Exploring the molecular mechanisms between lymphoma and myelofibrosis.American journal of translational research · 2024
    Review
  6. Review
  7. Diagnosis- and Prognosis-Related Gene Alterations inInternational journal of molecular sciences · 2023
    Review
  8. Article
  9. Review
  10. Review
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  13. 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

29 authors at 15 institutions in 1 country.

F Ferrer-Marín *Hospital Morales Meseguer, Centro Regional de Hemodonación, IMIB-Arrixaca, Murcia, Spain. fferrermarin@gmail.com.
A B Arroyo *Hospital Morales Meseguer, Centro Regional de Hemodonación, IMIB-Arrixaca, Murcia, Spain.
B BellosilloHospital del Mar (IMIM), Barcelona, Spain.
E J CuencaHospital Morales Meseguer, Centro Regional de Hemodonación, IMIB-Arrixaca, Murcia, Spain.
L ZamoraICO-Badalona, Institut d'Investigació contra la Leucèmia Josep Carreras, Badalona, Spain.
J M Hernández-RivasHospital Universitario de Salamanca, Salamanca, Spain.
J C Hernández-BoludaHospital Clínico, Valencia, Spain.ORCID http://orcid.org/0000-0002-4289-3113
C Fernandez-RodriguezHospital del Mar (IMIM), Barcelona, Spain.
E LuñoHospital Central de Asturias, Oviedo, Spain.
C García HernandezHospital General de Alicante, Alicante, Spain.
A KerguelenHospital La Paz, Madrid, Spain.
D V Fiallo-SuárezHospital Universitario Dr Negrín, Las Palmas de Gran Canaria, Spain.
M T Gómez-CasaresHospital Universitario Dr Negrín, Las Palmas de Gran Canaria, Spain.
R AyalaHospital Doce de Octubre, UCM, CNIO, CIBERONC, Madrid, Spain.
P VélezICO-Hospital Duran y Reynals, Barcelona, Spain.
C BoquéICO-Hospital Duran y Reynals, Barcelona, Spain.
V García-GutierrezHospital Universitario Ramón y Cajal, Madrid, Spain.
B ArrizabalagaHospital Universitario de Cruces, Bilbao, Spain.
N EstradaICO-Badalona, Institut d'Investigació contra la Leucèmia Josep Carreras, Badalona, Spain.
R CifuentesHospital Morales Meseguer, Centro Regional de Hemodonación, IMIB-Arrixaca, Murcia, Spain.
I ArcasServicio de Anatomía Patológica, Hospital General Universitario Reina Sofía, Murcia, Spain.
A M de Los Reyes-GarcíaHospital Morales Meseguer, Centro Regional de Hemodonación, IMIB-Arrixaca, Murcia, Spain.
C BessesHospital del Mar (IMIM), Barcelona, Spain.
V VicenteHospital Morales Meseguer, Centro Regional de Hemodonación, IMIB-Arrixaca, Murcia, Spain.
A Alvarez-LarránHospital del Mar (IMIM), Barcelona, Spain.
R Teruel-MontoyaHospital Morales Meseguer, Centro Regional de Hemodonación, IMIB-Arrixaca, Murcia, Spain.
R González-ConejeroHospital Morales Meseguer, Centro Regional de Hemodonación, IMIB-Arrixaca, Murcia, Spain.
C MartínezHospital Morales Meseguer, Centro Regional de Hemodonación, IMIB-Arrixaca, Murcia, Spain.
GEMFIN Group
Centro Regional de Hemodonación · ESHospital Del Mar · ESCentre for Biomedical Network Research on Rare Diseases · ESDuran i Reynals Hospital · ESFundación Josep Carreras Contra la Leucemia · ESHospital Universitario de Gran Canaria Doctor Negrín · ESComplejo Hospitalario de Salamanca · ESHospital Clínico Universitario de Valencia · ESHospital de Cruces · ESHospital General Universitario de Alicante Doctor Balmis · ESHospital Reina Sofía de Murcia · ESHospital Universitario 12 De Octubre · ESHospital Universitario Central de Asturias · ESHospital Universitario La Paz · ESHospital Universitario Ramón y Cajal · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myelofibrosis (MF) occurs as part of the natural history of polycythemia vera (PV) and essential thrombocythemia (ET), and remarkably shortens survival. Although JAK2V617F and CALR allele burden are the main transformation risk factors, inflammation plays a critical role by driving clonal expansion toward end-stage disease. NF-κB is a key mediator of inflammation-induced carcinogenesis. Here, we explored the involvement of miR-146a, a brake in NF-κB signaling, in MPN susceptibility and progression. rs2910164 and rs2431697, that affect miR-146a expression, were analyzed in 967 MPN (320 PV/333 ET/314 MF) patients and 600 controls. We found that rs2431697 TT genotype was associated with MF, particularly with post-PV/ET MF (HR = 1.5; p < 0.05). Among 232 PV/ET patients (follow-up time=8.5 years), 18 (7.8%) progressed to MF, being MF-free-survival shorter for rs2431697 TT than CC + CT patients (p = 0.01). Multivariate analysis identified TT genotype as independent predictor of MF progression. In addition, TT (vs. CC + CT) patients showed increased plasma inflammatory cytokines. Finally, miR-146a

Indexed as

AgedAllelesAnimalsCytokinesDisease ProgressionFemaleGenotypeHumansInflammationMaleMiceMice, Inbred C57BLMicroRNAsMiddle AgedMutationMyeloproliferative DisordersCytokinesMicroRNAsMIRN146 microRNA, humanNF-kappa B

Identifiers

PMID32107471
OpenAlexW3007570521

What OpenQuestion holds

Textmetadata
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.