Evidence map›Paper›PMID 32685486›Full record

ArticleBioMed research international2020

Yuping Zeng, He He, Yu Zhang, Xia Wang, Lidan Yang, Zhenmei An

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  4. ASPM promotes ATR-CHK1 activation and stabilizes stalled replication forks in response to replication stress.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  5. Oxidative medicine and cellular longevity · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. 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

6 authors at 1 institution in 1 country.

Yuping ZengDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, China.ORCID https://orcid.org/0000-0003-2837-2394
He HeDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, China.
Yu ZhangDepartment of Endocrine and Metabolism, West China Hospital, Sichuan University, Chengdu, China.
Xia WangDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, China.ORCID https://orcid.org/0000-0002-0881-3538
Lidan YangDepartment of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, China.
Zhenmei AnDepartment of Endocrine and Metabolism, West China Hospital, Sichuan University, Chengdu, China.ORCID https://orcid.org/0000-0001-5952-3701
Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is characterized by increased mortality and poor prognosis. We aimed to identify potential prognostic markers by weighted gene coexpression network analysis (WGCNA), to assist clinical outcome prediction and improve treatment decisions for HCC patients.

methodsPrognosis-related gene modules were first established by WGCNA. Venn diagrams obtained intersection genes of module genes and differentially expressed genes. The Kaplan-Meier overall survival curves and disease-free survival curves of intersection genes were further analyzed on the Gene Expression Profiling Interactive Analysis website. Chi-square tests were performed to explore the associations between prognostic gene expressions and clinicopathological features.

results

conclusionOverexpression of

Indexed as

Gene Expression Regulation, NeoplasticGene Regulatory NetworksCarcinoma, HepatocellularCyclin B2DNA Topoisomerases, Type IIFemaleGenes, NeoplasmHumansLiver NeoplasmsMaleMiddle AgedNerve Tissue ProteinsPoly-ADP-Ribose Binding ProteinsPrognosisReproducibility of ResultsSurvival AnalysisASPM protein, humanCCNB2 protein, humanCyclin B2DNA Topoisomerases, Type IINerve Tissue ProteinsPoly-ADP-Ribose Binding ProteinsTOP2A protein, human

Identifiers

PMID32685486
PMCPMC7333053
OpenAlexW3037341347

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.