Evidence map›Paper›PMID 32170852›Full record

ArticleCancer medicine2020

Identification of aberrantly methylated differentially expressed genes and associated pathways in endometrial cancer using integrated bioinformatic analysis.

JinHui Liu, YiCong Wan, Siyue Li, HuaiDe Qiu, Yi Jiang, Xiaoling Ma, ShuLin Zhou, WenJun Cheng

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

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  14. HypermethylatedFrontiers in oncology · 2022
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  20. The New Paradigm of Network Medicine to Analyze Breast Cancer Phenotypes.International journal of molecular sciences · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

JinHui LiuDepartment of Gynecology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
YiCong WanDepartment of Gynecology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Siyue LiDepartment of Gynecology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
HuaiDe QiuCenter of Rehabilitation Medicine, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Yi JiangDepartment of Gynecology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Xiaoling MaDepartment of Gynecology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
ShuLin ZhouDepartment of Gynecology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
WenJun ChengDepartment of Gynecology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.ORCID 0000-0002-3872-4384
Jiangsu Province Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endometrial cancer (EC) is a fatal female reproductive tumor. Bioinformatic tools are increasingly developed to screen out molecular targets related to EC. In this study, GSE17025 and GSE40032 were obtained from Gene Expression Omnibus (GEO). "limma" package and Venn diagram tool were used to identify hub genes. FunRich was used for functional analysis. Retrieval of Interacting Genes Database (STRING) was used to analyze protein-protein interaction (PPI) complex. Cancer Genome Atlas (TCGA), GEPIA, immunohistochemistry staining, and ROC curve analysis were carried out for validation. Univariate and multivariate regression analyses were performed to predict the risk score. Compound muscle action potential (CMap) was used to find potential drugs. GSEA was also done. We retrieved seven oncogenes which were upregulated and hypomethylated and 12 tumor suppressor genes (TSGs) which were downregulated and hypermethylated. The upregulated and hypomethylated genes were strikingly enriched in term "immune response" while the downregulated and hypermethylated genes were mainly focused on term "aromatic compound catabolic process." TCGA and GEPIA were used to screen out EDNRB, CDO1, NDN, PLCD1, ROR2, ESPL1, PRAME, and PTTG1. Among them, ESPL1 and ROR2 were identified by Cox regression analysis and were used to construct prognostic risk model. The result showed that ESPL1 was a negative independent prognostic factor. Cmap identified aminoglutethimide, luteolin, sulfadimethoxine, and maprotiline had correlation with EC. GSEA results showed that "hedgehog signaling pathway" was enriched. This research inferred potential aberrantly methylated DEGs and dysregulated pathways may participate in EC development and firstly reported eight hub genes, including EDNRB, CDO1, NDN, PLCD1, ROR2, ESPL1, PRAME, and PTTG1 that could be used to predict EC prognosis. Aminoglutethimide and luteolin may be used to fight against EC.

Indexed as

DNA MethylationComputational BiologyDatabases, GeneticEndometrial NeoplasmsFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHedgehog ProteinsHumansPrognosisProportional Hazards ModelsProtein Interaction MapsReceptor Tyrosine Kinase-like Orphan ReceptorsReproducibility of ResultsSeparaseSmall Molecule LibrariesESPL1 protein, humanHedgehog ProteinsReceptor Tyrosine Kinase-like Orphan ReceptorsROR2 protein, humanSeparaseSmall Molecule Librariesbioinformatic analysisCMapendometrial cancergene expression omnibus (GEO)methylationPPIrisk model

Identifiers

PMID32170852
PMCPMC7221444
OpenAlexW3011141263

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.