Evidence map›Paper›PMID 32862280›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2021

A three-gene signature and clinical outcome in pediatric acute myeloid leukemia.

Z Cai, Y Wu, F Zhang, H Wu

Abstract read
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In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. The multifaceted roles of ribosomal P complex in cancer.World journal of surgical oncology · 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

4 authors at 3 institutions in 1 country.

Z CaiDepartment of Pediatrics, The First Affiliated Hospital of University of South China, Hengyang, 421001, Hunan, China.
Y WuDepartment of Pathology, The First People's Hospital of Xiangtan City, No.100 Shuyuan Road, Yuetang District, Xiangtan, 421001, Hunan, China.
F ZhangDepartment of Pathology, The Rushan People's Hospital of Weihai City, Shandong, 264500, China.
H WuDepartment of Pathology, The First People's Hospital of Xiangtan City, No.100 Shuyuan Road, Yuetang District, Xiangtan, 421001, Hunan, China. w289244617@csu.edu.cn.ORCID http://orcid.org/0000-0002-8207-0736
Xiangshan County First People's Hospital · CNFirst Affiliated Hospital of University of South China · CNWeihai Municipal Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough the 5-year survival rates in pediatric acute myeloid leukemia (AML) have improved over the last decades, there is a high relapse rate for Pediatric AML patients.

methodsIn the present study, we mainly combine PCA with the LASSO technique to identify prognostic markers for Pediatric AML patients coming from the NCI TARGET database.

resultsThree key genes (EEF1A1, RPLP2, RPL19) associated with poor prognosis of pediatric AML has been screened by both PCA and LASSO Cox regression analysis. Simultaneously, we developed a risk score model to predict the prognosis of pediatric AML, according to risk scores, the patients were divided into high- and low-risk groups based on the median risk score. Kaplan-Meier survival analysis indicated that Pediatric AML patients with the high-risk group have a poorer survival rate than those with a low-risk group (p < 0.000). The receiver operating characteristic (ROC) analysis showed that the risk model has a good performance (AUC:0.669). Moreover, the clinicopathologic correlation showed that the expression levels of three genes were related to the central nervous system (CNS) disease and chloroma. GSEA identified that those pathways including oxidative phosphorylation, apoptosis and TGFB signaling pathway were differentially enriched.

conclusionTaken together, those studies suggested that a gene panel that consists of three genes (EEF1A1, RPLP2, RPL19) may act as a potential prognostic marker.

Indexed as

ApoptosisArea Under CurveBiomarkers, TumorCentral Nervous System NeoplasmsChildDatabases, FactualHomeodomain ProteinsHumansKaplan-Meier EstimateLeukemia, Myeloid, AcuteOxidative PhosphorylationPeptide Elongation Factor 1PhosphoproteinsPrognosisProportional Hazards ModelsRepressor ProteinsBiomarkers, TumorEEF1A1 protein, humanHomeodomain ProteinsPeptide Elongation Factor 1phosphoprotein P2, ribosomalPhosphoproteinsRepressor ProteinsRibosomal ProteinsRPL19 protein, humanTGIF1 protein, humanAMLGSEALASSOPediatricPrognosis

Identifiers

PMID32862280
OpenAlexW3081945993

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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.