Evidence map›Paper›PMID 32180907›Full record

ArticleMediterranean journal of hematology and infectious diseases2020

MicroRNA-181a-3p as a Diagnostic and Prognostic Biomarker for Acute Myeloid Leukemia.

Ping Qiang, Qing Pan, Chao Fang, Claudio Fozza, Kaidi Song, Yuanyuan Dai, Wenjiao Chang, Wei Chen, Wan Yao, Weibo Zhu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Mediterranean journal of hematology and infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

6 citing papers in PubMed, 16 citations in OpenAlex.

  1. miR-330-3p Inhibits the Development of Acute Myeloid Leukemia by Targeting SYTL4.APMIS : acta pathologica, microbiologica, et immunologica Scandinavica · 2026
    Article
  2. Constitutive systemic inflammation in Shwachman-Diamond Syndrome.Molecular medicine (Cambridge, Mass.) · 2025
    Article
  3. Expert opinion on therapeutic targets · 2024
    Review
  4. Article
  5. Gga-miR-181a modulates ANP32A expression and inhibits MDCC-MSB-1 cell.In vitro cellular & developmental biology. Animal · 2021
    Article
  6. 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

12 authors at 1 institution in 1 country.

Ping QiangSchool of Medicine, Shandong University, Jinan, 250100, China.
Qing PanThe First Hospital Affiliated to Anhui University of Traditional Chinese Medicine, Hefei, 230001, China.
Chao FangDepartment of Laboratory Medicine, The First Affiliated Hospital of University of Science and Technology of China, Hefei, 230001, China.
Claudio FozzaUniversity of Sassari, Sassari, Italy.
Kaidi SongDepartment of Hematology, The First Affiliated Hospital of University of Science and Technology of China, Hefei, 230001, China.
Yuanyuan DaiDepartment of Laboratory Medicine, The First Affiliated Hospital of University of Science and Technology of China, Hefei, 230001, China.
Wenjiao ChangDepartment of Laboratory Medicine, The First Affiliated Hospital of University of Science and Technology of China, Hefei, 230001, China.
Wei ChenSchool of Computer Science, University of Science and Technology of China, Hefei, 230001, China.
Wan YaoSchool of clinical medical, University of medical of Anhui, Hefei, 230001, China.
Weibo ZhuDepartment of Hematology, The First Affiliated Hospital of University of Science and Technology of China, Hefei, 230001, China.
Xin LiuDepartment of Hematology, The First Affiliated Hospital of University of Science and Technology of China, Hefei, 230001, China.
Xiaoling MaSchool of Medicine, Shandong University, Jinan, 250100, China.
Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicro (mi) RNAs play an important role in the pathogenesis and development of acute myeloid leukemia (AML), and their abnormal expression may be sufficient to predict the prognosis and outcomes in AML patients. We evaluated the clinical diagnostic value of miRNA-181a-3p in predicting prognosis and outcomes in patients with AML.

methodsA total of 119 newly diagnosed adult patients with AML and 60 healthy controls were recruited. Blood specimens were obtained from all AML patients at diagnosis, and 10 blood specimens were obtained on day 28 after induction chemotherapy. The controls also provided blood samples. Relative gene expression was quantified by PCR and determined using the comparative Ct method. Publicly available clinical data and gene expressions for 188 patients with AML were downloaded from TCGA data portal.

resultsCompared with healthy controls, the expression of miRNA-181a-3p was significantly increased in patients with AML. MiR-181a-3p expression could be used to discriminate AML patients from controls, with up-regulated expression correlating with favorable prognosis. Moreover, miRNA-181a-3p expression was significantly decreased in patients who achieved a complete response after induction chemotherapy. The multivariate Cox analysis highlighted the prognostic value of miR-181a-3p for patients with AML. Finally, we found that miR-181a-3p expression was negatively correlated with the expression of the NF-κB essential modulator (NEMO/IKBKG).

conclusionsMiR-181a-3p may be clinically useful as a disease marker for AML, and enhanced the prediction of patient outcomes to chemotherapy.

Indexed as

AcuteBiomarkersLeukemiaMicroRNAsMiR-181a-3pMyeloidTreatment outcome

Identifiers

PMID32180907
PMCPMC7059742
OpenAlexW3008893670

What OpenQuestion holds

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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.