Evidence map›Paper›PMID 24955371›Full record

ArticleBioMed research international2014

Prospective evaluation of whole genome microRNA expression profiling in childhood acute lymphoblastic leukemia.

Muhterem Duyu, Burak Durmaz, Cumhur Gunduz, Canan Vergin, Deniz Yilmaz Karapinar, Serap Aksoylar, Kaan Kavakli, Nazan Cetingul, Gulersu Irken, Yontem Yaman and 2 more

Open access · hybridAbstract readEvaluation Study
In one paragraph

Article in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

  1. Association Between theFrontiers in genetics · 2020
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  9. microRNA-155-5p initiates childhood acute lymphoblastic leukemia by regulating the IRF4/CDK6/CBL axis.Laboratory investigation; a journal of technical methods and pathology · 2022
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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

12 authors at 3 institutions in 1 country.

Muhterem DuyuDepartment of Pediatrics, Faculty of Medicine, Ege University, 35100 Izmir, Turkey.
Burak DurmazDepartment of Medical Genetics, Faculty of Medicine, Ege University, Bornova, 35100 Izmir, Turkey.
Cumhur GunduzDepartment of Medical Biology, Faculty of Medicine, Ege University, 35100 Izmir, Turkey.
Canan VerginDepartment of Pediatric Hematology, Behcet Uz Children's Hospital, 35210 Izmir, Turkey.
Deniz Yilmaz KarapinarDepartment of Pediatrics, Faculty of Medicine, Ege University, 35100 Izmir, Turkey.
Serap AksoylarDepartment of Pediatrics, Faculty of Medicine, Ege University, 35100 Izmir, Turkey.
Kaan KavakliDepartment of Pediatrics, Faculty of Medicine, Ege University, 35100 Izmir, Turkey.
Nazan CetingulDepartment of Pediatrics, Faculty of Medicine, Ege University, 35100 Izmir, Turkey.
Gulersu IrkenDepartment of Pediatrics, Faculty of Medicine, Dokuz Eylul University, 35340 Izmir, Turkey.
Yontem YamanDepartment of Pediatric Hematology, Behcet Uz Children's Hospital, 35210 Izmir, Turkey.
Ferda OzkinayDepartment of Pediatrics, Faculty of Medicine, Ege University, 35100 Izmir, Turkey.
Ozgur CoguluDepartment of Pediatrics, Faculty of Medicine, Ege University, 35100 Izmir, Turkey.
Ege University · TRDr. Behçet Uz Çocuk Hastalıkları Hastanesi · TRDokuz Eylül University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dysregulation of microRNA (miRNA) expression contributes to the pathogenesis of several clinical conditions. The aim of this study is to evaluate the associations between miRNAs and childhood acute lymphoblastic leukemia (ALL) to discover their role in the course of the disease. Forty-three children with ALL and 14 age-matched healthy controls were included in the study. MicroRNA microarray expression profiling was used for peripheral blood and bone marrow samples. Aberrant miRNA expressions associated with the diagnosis and outcome were prospectively evaluated. Confirmation analysis was performed by real time RT-PCR. miR-128, miR-146a, miR-155, miR-181a, and miR-195 were significantly dysregulated in ALL patients at day 0. Following a six-month treatment period, the change in miRNA levels was determined by real time RT-PCR and expression of miR-146a, miR-155, miR-181a, and miR-195 significantly decreased. To conclude, these miRNAs not only may be used as biomarkers in diagnosis of ALL and monitoring the disease but also provide new insights into the potential roles of them in leukemogenesis.

Indexed as

AdolescentCarcinogenesisChildChild, PreschoolFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGenome, HumanHumansMaleMicroRNAsPrecursor Cell Lymphoblastic Leukemia-LymphomaMicroRNAs

Identifiers

PMID24955371
PMCPMC4053274
OpenAlexW2144588259

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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.