Evidence map›Paper›PMID 36303086›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2023

MELTF Might Regulate Ferroptosis, Pyroptosis, and Autophagy in Platelet-Rich Plasma-Mediated Endometrial Epithelium Regeneration.

Yanhong Mao, Mei Wang, Yao Xiong, Xue Wen, Ming Zhang, Ling Ma, Yuanzhen Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Reproductive sciences (Thousand Oaks, Calif.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
1.5field-weighted citation impact, top 17% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 19 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Yanhong MaoCenter for Reproductive Medicine, Zhongnan Hospital of Wuhan University, NO. 169, East Lake Road, Wuchang District, Wuhan City, 430071, Hubei Province, China.ORCID 0000-0001-9525-2291
Mei WangCenter for Reproductive Medicine, Zhongnan Hospital of Wuhan University, NO. 169, East Lake Road, Wuchang District, Wuhan City, 430071, Hubei Province, China.
Yao XiongCenter for Reproductive Medicine, Zhongnan Hospital of Wuhan University, NO. 169, East Lake Road, Wuchang District, Wuhan City, 430071, Hubei Province, China.
Xue WenCenter for Reproductive Medicine, Zhongnan Hospital of Wuhan University, NO. 169, East Lake Road, Wuchang District, Wuhan City, 430071, Hubei Province, China.
Ming ZhangCenter for Reproductive Medicine, Zhongnan Hospital of Wuhan University, NO. 169, East Lake Road, Wuchang District, Wuhan City, 430071, Hubei Province, China.
Ling Ma *Center for Reproductive Medicine, Zhongnan Hospital of Wuhan University, NO. 169, East Lake Road, Wuchang District, Wuhan City, 430071, Hubei Province, China. 810323923@qq.com.ORCID 0000-0002-4344-7027
Yuanzhen Zhang *Center for Reproductive Medicine, Zhongnan Hospital of Wuhan University, NO. 169, East Lake Road, Wuchang District, Wuhan City, 430071, Hubei Province, China. zhangyuanzhen@whu.edu.cn.ORCID 0000-0003-4832-7902
Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The endometrial basal layer is essential for endometrial regeneration, whose disruption leads to thin endometrium or intrauterine adhesion (IUA) with an unsatisfactory prognosis. Emerging data indicate that platelet-rich plasma (PRP) can promote endometrial proliferation, but the mechanism by which PRP regulates endometrial regeneration remains unclear. Herein, we investigated the therapeutic effects and possible mechanisms of PRP on endometrial regeneration. IUA animal model was generated by sham, mechanically damaging endometrium with or without PRP for 10 days. The uterine section in the model group showed degenerative changes with a narrow endometrial lumen, atrophic columnar epithelium, decreased number of endometrial glands, decreased endometrial thickness, and increased collagen deposition. The above disruption could be ameliorated by the PRP. Transcriptome sequencing analysis displayed that the retinol metabolism pathway and extracellular matrix (ECM) receptor interaction pathway were up-regulated and enriched in differential expression genes (DEGs). Melanotransferrin (MELTF) was the key up-regulated gene in PRP-induced endometrial regeneration, which was verified in vivo and in vitro. Ferroptosis, autophagy, and pyroptosis were down-regulated in PRP-treated Ishikawa cells. Conclusively, PRP promotes endometrium regeneration by up-regulating the retinol metabolism and ECM receptor interaction pathway with MELTF. Meanwhile, PRP could also inhibit endometrial epithelial cell death by regulating ferroptosis, autophagy, and pyroptosis.

Indexed as

FerroptosisPlatelet-Rich PlasmaUterine DiseasesAnimalsAutophagyDisease Models, AnimalEndometriumEpitheliumFemaleHumansMembrane GlycoproteinsPyroptosisRegenerationVitamin AMELTF protein, humanMembrane GlycoproteinsVitamin AEndometrial regenerationIntrauterine adhesionMELTFPRPTranscriptome sequencing analysis

Identifiers

PMID36303086
OpenAlexW4307407951

What OpenQuestion holds

Textmetadata
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.