Evidence map›Paper›PMID 34130686›Full record

ArticleBMC endocrine disorders2021

The role of FDX1 in granulosa cell of Polycystic ovary syndrome (PCOS).

Zhi Wang, Hui Dong, Li Yang, Ping Yi, Qing Wang, Dongmei Huang

Open access · goldAbstract read
In one paragraph

Article in BMC endocrine disorders, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
11.2field-weighted citation impact, top 1% 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, 60 citations in OpenAlex.

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  6. Liraglutide Improves PCOS Symptoms in Rats by Targeting FDX1.Reproductive sciences (Thousand Oaks, Calif.) · 2024
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  11. FDX1 enhances endometriosis cell cuproptosis via G6PD-mediated redox homeostasis.Apoptosis : an international journal on programmed cell death · 2023
    Article
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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

6 authors at 2 institutions in 1 country.

Zhi WangDepartment of Integrated Traditional Chinese and Western Medicine, Tongji hospital, Huazhong University of Science and Technology, Jiefang Road 1095#, 430030, Wuhan, China.
Hui DongInstitute of Integrated Traditional Chinese and Western Medicine, Tongji hospital, Huazhong University of Science and Technology, Jiefang Road 1095 #, 430030, Wuhan, China.
Li YangDepartment of Integrated Traditional Chinese and Western Medicine, Tongji hospital, Huazhong University of Science and Technology, Jiefang Road 1095#, 430030, Wuhan, China.
Ping YiInstitute of Integrated Traditional Chinese and Western Medicine, Tongji hospital, Huazhong University of Science and Technology, Jiefang Road 1095 #, 430030, Wuhan, China.
Qing WangDepartment of Rehabilitation Center of Wuhan Puren Hospital, Affiliated Hospital of Wuhan, University of Science and Techn ology, Benxi Street 1#, Qingshan District, 430081, Wuhan, China.
Dongmei HuangInstitute of Integrated Traditional Chinese and Western Medicine, Tongji hospital, Huazhong University of Science and Technology, Jiefang Road 1095 #, 430030, Wuhan, China. hdmjcr@163.com.
Huazhong University of Science and Technology · CNWuhan University of Science and Technology · CN

Funding

National Natural Science Foundation of China 81573787National Natural Science Foundation of China 81673757National Natural Science Foundation of China 81874382
6 · The paper itself

Abstract

backgroundTo explore the development mechanism of PCOS and Transcriptomics was applied to seek the key gene.

methodsTranscriptomics marked by UID (unique identifier) technique of granulosa cell in PCOS and control women was carried out and key gene was picked up. Then the key gene in granulosa cell was measured by RT-PCR. Two PCOS models modeling with Letrozole and Testosterone Propionate were implemented and the key gene in granulosa cell of ovary was measured by immunohistochemistry to verify the relation with PCOS.

resultsGO-enrich of transcriptomics concentrated in domain steroid metabolism and domain mitochondria. Different genes were sought from coexisting in both domain steroid metabolism and domain mitochondria. Finally, five different genes including CYP11A1、CYB5R1、STAR、FDX1 and AMACR were obtained. RT-PCR was implemented to furtherly verify the downregulating mRNA of FDX1 in PCOS, which showed the consistent outcome with the transcriptomics. Level of FDX1 protein in granulosa cell of antral follicle in two PCOS models was measured and decreased.

conclusionsFDX1 was related with steroid metabolism and mitochondrial and may participate in the development of PCOS.

Indexed as

AdultBiomarkersCase-Control StudiesFemaleFerredoxinsFollow-Up StudiesGene Expression RegulationGranulosa CellsHumansPolycystic Ovary SyndromePrognosisRNA, MessengerTranscriptomeBiomarkersFerredoxinsRNA, MessengerFDX1PCOS

Identifiers

PMID34130686
PMCPMC8207664
OpenAlexW3172334485

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.