Evidence map›Paper›PMID 25550847›Full record

ArticleInternational journal of clinical and experimental pathology2014

Increased expression of miR-24 is associated with acute myeloid leukemia with t(8;21).

Jia-Yu Yin, Qin Tang, Wei Qian, Jun Qian, Jiang Lin, Xiang-Mei Wen, Jing-Dong Zhou, Ying-Ying Zhang, Xiao-Wen Zhu, Zhao-Qun Deng

Abstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Association Between theFrontiers in genetics · 2020
    Pooled it
  3. Review
  4. Review
  5. Review
  6. Article
  7. Expression of the miR-148/152 Family in Acute Myeloid Leukemia and its Clinical Significance.Medical science monitor : international medical journal of experimental and clinical research · 2017
    Article
  8. Article
  9. Article
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

10 authors.

Jia-Yu YinAffiliated People's Hospital of Jiangsu University Zhenjiang, Jiangsu, China.
Qin TangAffiliated People's Hospital of Jiangsu University Zhenjiang, Jiangsu, China.
Wei QianAffiliated People's Hospital of Jiangsu University Zhenjiang, Jiangsu, China.
Jun QianAffiliated People's Hospital of Jiangsu University Zhenjiang, Jiangsu, China.
Jiang LinAffiliated People's Hospital of Jiangsu University Zhenjiang, Jiangsu, China.
Xiang-Mei WenAffiliated People's Hospital of Jiangsu University Zhenjiang, Jiangsu, China.
Jing-Dong ZhouAffiliated People's Hospital of Jiangsu University Zhenjiang, Jiangsu, China.
Ying-Ying ZhangAffiliated People's Hospital of Jiangsu University Zhenjiang, Jiangsu, China.
Xiao-Wen ZhuAffiliated People's Hospital of Jiangsu University Zhenjiang, Jiangsu, China.
Zhao-Qun DengAffiliated People's Hospital of Jiangsu University Zhenjiang, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study was designed to learn the expression status of miR-24 and its clinical relevance in patients with acute myeloid leukemia (AML). We detected the miR-24 expression levels using real-time quantitative PCR in 84 AML patients and investigated the clinical significance of miR-24 expression in AML. There was no difference in clinical parameters between cases with miR-24 high expression and with miR-24 low expression. The frequency of miR-24 high expression was higher in patients with t(8;21) than in others (82% (9/11) versus 44% (32/72), P=0.026). The levels of miR-24 expression had no correlation with the mutations of nine genes (FLT3-ITD, NPM1, C-KIT, IDH1/IDH2, DNMT3A, N/K-RAS and C/EBPA). Meanwhile, among the group who obtained CR, the cases with miR-24 high expression had no difference in overall survival (OS) and relapse-free survival (RFS) than those with miR-24 low expression (P=0.612 and 0.665, respectively). These findings implicated that miR-24 high regulation is a common event in AML with t(8;21), and it might serve as a novel and selective therapeutic target for the treatment of AML with t(8;21).

Indexed as

Chromosomes, Human, Pair 21Chromosomes, Human, Pair 8Gene Expression Regulation, LeukemicTranslocation, GeneticAdolescentAdultAgedAged, 80 and overChildFemaleHumansLeukemia, Myeloid, AcuteMaleMicroRNAsMiddle AgedMutationMicroRNAsMIRN24 microRNA, humanNPM1 protein, humanNucleophosminacute myeloid leukemiamicroRNAmiR-24

Identifiers

PMID25550847
PMCPMC4270540

What OpenQuestion holds

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Read underepoch 390

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.