Evidence map›Paper›PMID 36047377›Full record

ArticleJournal of gynecologic oncology2022

Prognostication of early-onset endometrioid endometrial cancer based on genome-wide DNA methylation profiles.

Takuro Hirano, Eri Arai, Mao Fujimoto, Yuji Nakayama, Ying Tian, Nanako Ito, Takeshi Makabe, Wataru Yamagami, Nobuyuki Susumu, Daisuke Aoki and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of gynecologic oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
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  4. Analysis ofInternational journal of molecular sciences · 2024
    Observational
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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

11 authors at 1 institution in 1 country.

Takuro HiranoDepartment of Pathology, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-1175-1614
Eri AraiDepartment of Pathology, Keio University School of Medicine, Tokyo, Japan. earai@keio.jp.ORCID 0000-0002-0076-4823
Mao FujimotoDepartment of Pathology, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-2020-935X
Yuji NakayamaDepartment of Pathology, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-9069-6333
Ying TianDepartment of Pathology, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-7683-5261
Nanako ItoDepartment of Pathology, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-4704-4137
Takeshi MakabeDepartment of Pathology, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-0443-2527
Wataru YamagamiDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0003-3925-6057
Nobuyuki SusumuDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-3537-7161
Daisuke AokiDepartment of Obstetrics and Gynecology, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-9596-8326
Yae KanaiDepartment of Pathology, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-7904-9506
Keio University · JP

Funding

Japan Agency for Medical Research and Development 20ae0101020h0005
6 · The paper itself

Abstract

objectiveThe aim of this study was to establish criteria that would indicate whether fertility preservation therapy would likely be safe for patients aged 40 years or less with endometrioid endometrial cancer based on their DNA methylation profile.

methodsForty-nine fresh-frozen tissue samples from patients with endometrial cancer from an initial cohort and 31 formalin-fixed paraffin-embedded tissue samples from a second cohort were subjected to genome-wide DNA methylation analysis using the Infinium MethylationEPIC BeadChip.

resultsEpigenomic clustering of early-onset endometrial cancer was correlated with the widely used recurrence risk classification. Genes showing differences in DNA methylation levels between the low-recurrence-risk category and intermediate- and high-risk categories were accumulated in pathways related to fibroblast growth factor and nuclear factor-κB signaling. DNA hypomethylation and overexpression of

conclusionsDNA methylation diagnostics criteria using up to 6 of 8 CpG sites for

Indexed as

Carcinoma, EndometrioidDNA MethylationEndometrial NeoplasmsCpG IslandsFemaleHumansParaffin EmbeddingDNA MethylationEarly OnsetEndometrioid CarcinomaFertility PreservationInfinium ArrayZBTB38

Identifiers

PMID36047377
PMCPMC9634101
OpenAlexW4293082977

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.