Evidence map›Paper›PMID 30700251›Full record

ArticleBMC cancer2019

Selection of three miRNA signatures with prognostic value in non-M3 acute myeloid leukemia.

Yao Xue, Yuqiu Ge, Meiyun Kang, Cong Wu, Yaping Wang, Liucheng Rong, Yongjun Fang

Abstract read
In one paragraph

Article in BMC cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

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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

5 citing papers in PubMed.

  1. MircoRNAs predict and modulate responses to chemotherapy in leukemic patients.Naunyn-Schmiedeberg's archives of pharmacology · 2025
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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

7 authors.

Yao XueDepartment of Hematology and Oncology, Children's Hospital of Nanjing Medical University, Nanjing, China.
Yuqiu GeDepartment of Public Health and Preventive Medicine, Wuxi School of Medicine, Jiangnan University, Wuxi, China.
Meiyun KangDepartment of Hematology and Oncology, Children's Hospital of Nanjing Medical University, Nanjing, China.
Cong WuEngineering Research Center of Wideband Wireless Communication Technology, Ministry of Education, Nanjing University of Posts and Telecommunications, Nanjing, China.
Yaping WangDepartment of Hematology and Oncology, Children's Hospital of Nanjing Medical University, Nanjing, China.
Liucheng RongDepartment of Hematology and Oncology, Children's Hospital of Nanjing Medical University, Nanjing, China.
Yongjun FangDepartment of Hematology and Oncology, Children's Hospital of Nanjing Medical University, Nanjing, China. fyjpaper@163.com.ORCID http://orcid.org/0000-0002-6170-6950

Funding

Nanjing Medical Science and Technology Development Foundation QRX17164Nanjing Medical Science and Technology Development Project YKK15140Nanjing Science and Technology Development Foundation 201503043National Natural Science Foundation of China 81602913National Natural Science Foundation of China 81670155Natural Science Foundation of Jiangsu Province BK20150085Technology Development Foundation of Nanjing Medical University 2014NJMUZD079
6 · The paper itself

Abstract

backgroundMiRNAs that are potential biomarkers for predicting prognosis for acute myeloid leukemia (AML) have been identified. However, comprehensive analyses investigating the association between miRNA expression profiles and AML survival remain relatively deficient.

methodIn the present study, we performed multivariate Cox's analysis and principal component analysis (PCA) using data from The Cancer Genome Atlas (TCGA) to identify potential molecular signatures for predicting non-M3 AML prognosis.

resultWe found that patients who were still living were significantly younger at diagnosis than those who had died (P = 0.001). In addition, there was a marked difference in living status among different risk category groups (P = 0.022). A multivariate Cox model suggested that three miRNAs were potential biomarkers of non-M3 AML prognosis, including miR-181a-2, miR-25 and miR-362. Subsequently, PCA analyses were conducted to comprehensively represent the expression levels of these three miRNAs in each patient with a PCA value. According to the log-rank test, AML outcome for patients with lower PCA values was significantly different from those with higher PCA values (P < 0.001). Further bioinformatic analysis revealed the biological functions of the selected miRNAs.

conclusionWe conducted a comprehensive analysis of TCGA non-M3 AML data, identifying three miRNAs that are significantly correlated with AML survival. PCA values for the identified miRNAs are valuable for predicting AML prognosis.

Indexed as

AdultAgedBiomarkers, TumorDatabases, GeneticFemaleGene ExpressionHumansLeukemia, Myeloid, AcuteMaleMicroRNAsMiddle AgedModels, StatisticalPrincipal Component AnalysisPrognosisRisk FactorsSurvival AnalysisBiomarkers, TumorMicroRNAsAcute myeloid leukemiamiRNAsPrognosisTCGA data

Identifiers

PMID30700251
PMCPMC6483142

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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.