Evidence map›Paper›PMID 29540187›Full record

ArticleJournal of translational medicine2018

MiR-362-5p as a novel prognostic predictor of cytogenetically normal acute myeloid leukemia.

Qiu-Ling Ma, Jing-Han Wang, Min Yang, Huan-Ping Wang, Jie Jin

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.3field-weighted citation impact, top 24% 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

21 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  4. Frontiers in cellular and infection microbiology · 2025
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  6. Review
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  8. Article
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  11. Plasma exosome-derived microRNA-532 as a novel predictor for acute myeloid leukemia.Cancer biomarkers : section A of Disease markers · 2020
    Article
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  14. Review
  15. Article
  16. Article
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  19. Article
  20. MicroRNAs in Autoimmunity and Hematological Malignancies.International journal of molecular sciences · 2018
    Review
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

5 authors at 2 institutions in 1 country.

Qiu-Ling MaDepartment of Hematology, The First Affiliated Hospital, Zhejiang University of Medicine, No. 79 Qingchun Road, 310003, Hangzhou, Zhejiang, People's Republic of China.
Jing-Han WangDepartment of Hematology, The First Affiliated Hospital, Zhejiang University of Medicine, No. 79 Qingchun Road, 310003, Hangzhou, Zhejiang, People's Republic of China.
Min YangDepartment of Hematology, The First Affiliated Hospital, Zhejiang University of Medicine, No. 79 Qingchun Road, 310003, Hangzhou, Zhejiang, People's Republic of China.
Huan-Ping WangKey Laboratory of Hematopoietic Malignancies, Hangzhou, Zhejiang Province, People's Republic of China.
Jie JinDepartment of Hematology, The First Affiliated Hospital, Zhejiang University of Medicine, No. 79 Qingchun Road, 310003, Hangzhou, Zhejiang, People's Republic of China. jiej0503@zju.edu.cn.
First Affiliated Hospital Zhejiang University · CNHenan University of Traditional Chinese Medicine · CN

Funding

National Natural Science Foundation of China grants 81370643National Natural Science Foundation of China grants 81470305National Natural Science Foundation of China grants U1404806National Public Health Grand Research Foundation 201202017University Science and Technology Innovation Talent Support Program of Henan Province 17HASTIT046Zhejiang natural fund Y16H160037
6 · The paper itself

Abstract

backgroundMicroRNAs are of special interest in cancer research and hold significant promise as diagnostic and prognostic biomarkers for malignant disease. MiR-362-5p have been found to exert both oncogenic and tumor suppressive effects depending highly on the cellular context. The aim of this study was to determine whether the expression of miR-362-5p can be served as a prognostic factor for patients with cytogentically normal acute myeloid leukemia (CN-AML).

methodsWe enrolled 224 patients with CN-AML and measured the expression of miR-362-5p by quantitative real time PCR analysis. We classified patients into high and low expression based on the median value. The Cox regression analyses were carried out to assess the prognostic significance of miR-362-5p expression in the context of the well-established predictors. Additionally, microRNA expression profiling were conducted to identify the biological insights between high and low group.

resultsHigh expressers had older age. High expressers obtained shorter overall survival in the univariate analysis. The independent prognostic value of miR-362-5p remained in the context of the well-established clinical and cytogenetic predictors. Moreover, the prognostic value of miR-362-5p was also validated in an independent cohort of CN-AML. Notably, numerous oncomiRs were also high expressed in high miR-362-5p group.

conclusionHigh miR-362-5p expression was associated with poorer overall survival implicating the oncogenic function in AML development.

Indexed as

Cytogenetic AnalysisFemaleGene Expression ProfilingGene Expression Regulation, LeukemicHumansKaplan-Meier EstimateLeukemia, Myeloid, AcuteMaleMicroRNAsMiddle AgedPrognosisMicroRNAsMIRN362 microRNA, humanAcute myeloid leukemiaGene expressionmiR-362-5pPrognosis

Identifiers

PMID29540187
PMCPMC5853092
OpenAlexW2800081056

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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.