Evidence map›Paper›PMID 40021920›Full record

ArticleScientific reports2025

Identification of FZD7 as a potential ferroptosis-related diagnostic gene in endometriosis by bioinformatics analysis.

Jianyun Huang, Jinbo Li, Xiao Li, Hongling Guo, Shuqin Chen

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

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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

3 citing papers in PubMed.

  1. Review
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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

5 authors.

Jianyun Huang *Department of Gynecology, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Jinbo Li *Department of Gynecology, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xiao LiDepartment of Gynecology, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Hongling GuoDepartment of Gynecology, The Seventh Affiliated Hospital, Sun Yat-sen University, Shenzhen, China. kwokhling3@mail.sysu.edu.cn.
Shuqin ChenDepartment of Gynecology, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, China. chshqin@mail.sysu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An increasing number of research have suggested that ferroptosis plays an important role in endometriosis (EMS). This study was to identify a ferroptosis-related diagnosis gene in EMS by using bioinformatics. R Bioconductor package limma was used to analyzed the differentially expressed genes (DEGs) between the EMS groups and control groups. CIBERSORT was used to analyze the differences between the EMS group and control group of 22 immune cells. Quantitative real-time PCR (RT-qPCR) and Western blot (WB) were used to validate the expression level of FZD7 in tissue samples. The study found that FZD7 was upregulated and showed good diagnostic value in five EMS transcriptome databases. RT-qPCR and WB experiments also verified that FZD7 was upregulated in EMS. Moreover, we found that macrophages, especially M2 macrophages, were significantly infiltrated in EMS. FZD7 was positively correlated with M2 macrophage infiltration, and was up-regulated in the endometrial stromal cells co-cultured with macrophages. The study identified an ferroptosis repressor gene, FZD7, validated in five EMS transcriptome datasets, which is significantly up-regulated in ectopic lesions of EMS and is a potential target for the treatment of EMS.

Indexed as

EndometriosisFerroptosisFrizzled ReceptorsAdultAnimalsBiomarkersComputational BiologyDisease Models, AnimalFemaleGene Expression ProfilingHumansMiceMice, Inbred BALB CUp-RegulationYoung AdultBiomarkersFrizzled ReceptorsFZD7 protein, humanFzd7 protein, mouseBioinformatics analysisEndometriosisFerroptosisFZD7

Identifiers

PMID40021920
PMCPMC11871347

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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.