Evidence map›Paper›PMID 31411110›Full record

ArticleBioengineered2019

Clinical significance of serum MicroRNA-203 in patients with acute myeloid leukemia.

Yingmeng Guo

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Bioengineered, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 40% 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, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. MicroRNAs in Vascular Eye Diseases.International journal of molecular sciences · 2020
    Review
  4. Article
  5. Review
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Yingmeng Guoa Department of Pediatric medicine, Linyi Central Hospital , Yishui , China.ORCID 0000-0002-7312-3664
Linyi People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to detect serum miR-203 expression levels in AML and explore its potential clinical significance. Quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) was performed to measure the serum miR-203 levels in 134 patients with AML and 70 healthy controls. The results demonstrated that serum miR-203 expression was significantly reduced in AML patients compared with healthy controls. Receiver operating characteristic curve (ROC) analysis revealed miR-203 could distinguish AML cases from normal controls. Low serum miR-203 levels were associated with worse clinical features, as well as poorer overall survival and relapse free survival of AML patients. Moreover, multivariate analysis confirmed low serum miR-203 expression to be an independent unfavorable prognostic predictor for AML. The bioinformatics analysis showed that the downstream genes and pathways of miR-203 was closely associated with tumorigenesis. Downregulation of miR-203 in AML cell lines upregulated the expression levels of oncogenic promoters such as CREB1, SRC and HDAC1. Thus, these findings demonstrated that serum miR-203 might be a promising biomarker for the diagnosis and prognosis of AML.

Indexed as

Gene Expression Regulation, LeukemicAntagomirsBiomarkers, TumorCarcinogenesisCase-Control StudiesCell Line, TumorComputational BiologyCyclic AMP Response Element-Binding ProteinGene Expression ProfilingGene OntologyHistone Deacetylase 1HumansLeukemia, Myeloid, AcuteMicroRNAsMolecular Sequence AnnotationMultivariate AnalysisAntagomirsBiomarkers, TumorCREB1 protein, humanCyclic AMP Response Element-Binding ProteinHDAC1 protein, humanHistone Deacetylase 1MicroRNAsMIRN203 microRNA, humanNeoplasm Proteinssrc-Family Kinasesacute myeloid leukemiadiagnosisprognosisserum miR-203

Identifiers

PMID31411110
PMCPMC6738448
OpenAlexW2969041506

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.