Evidence map›Paper›PMID 38044324›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Excessive Lipid Peroxidation in Uterine Epithelium Causes Implantation Failure and Pregnancy Loss.

Yafang Lu, Yuhan Shao, Weiwei Cui, Zhaoyu Jia, Qian Zhang, Qing Zhao, Zi-Jiang Chen, Junhao Yan, Bo Chu, Jia Yuan

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 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

10 authors at 1 institution in 1 country.

Yafang LuAdvanced Medical Research Institute, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.
Yuhan ShaoCenter for Reproductive Medicine, Shandong University, Jinan, Shandong, 250021, China.
Weiwei CuiDepartment of Cell Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.
Zhaoyu JiaAdvanced Medical Research Institute, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.
Qian ZhangCenter for Reproductive Medicine, Shandong University, Jinan, Shandong, 250021, China.
Qing ZhaoCenter for Reproductive Medicine, Shandong University, Jinan, Shandong, 250021, China.
Zi-Jiang ChenCenter for Reproductive Medicine, Shandong University, Jinan, Shandong, 250021, China.
Junhao YanCenter for Reproductive Medicine, Shandong University, Jinan, Shandong, 250021, China.
Bo ChuDepartment of Cell Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.
Jia YuanAdvanced Medical Research Institute, Cheeloo College of Medicine, Shandong University, Jinan, Shandong, 250012, China.ORCID 0000-0002-4807-8646
Shandong University · CN

Funding

Cutting Edge Development Fund of Advanced Medical Research InstituteNational Key Research and Development Program of China 2021YFC2700604National Key Research and Development Program of China 2022YFA0912600National Key Research and Development Program of China 2022YFC2702400National Natural Science Foundation of China 32000515National Natural Science Foundation of China 32270906National Natural Science Foundation of China 82171648Natural Science Foundation of Shandong Province 2022HWYQ-054Natural Science Foundation of Shandong Province ZR2020QC074Taishan Scholars Program for Young Experts of Shandong Province tsqn202103023
6 · The paper itself

Abstract

The uterine epithelium undergoes a dramatic spatiotemporal transformation to enter a receptive state, involving a complex interaction between ovarian hormones and signals from stromal and epithelial cells. Redox homeostasis is critical for cellular physiological steady state; emerging evidence reveals that excessive lipid peroxides derail redox homeostasis, causing various diseases. However, the role of redox homeostasis in early pregnancy remains largely unknown. It is found that uterine deletion of Glutathione peroxidase 4 (GPX4), a key factor in repairing oxidative damage to lipids, confers defective implantation, leading to infertility. To further pinpoint Gpx4's role in different cell types, uterine epithelial-specific Gpx4 is deleted by a lactotransferrin (Ltf)-Cre driver; the resultant females are infertile, suggesting increased lipid peroxidation levels in uterine epithelium compromises receptivity and implantation. Lipid peroxidation inhibitor administration failed to rescue implantation due to carbonylation of major receptive-related proteins underlying high lipid reactive oxygen species. Intriguingly, superimposition of Acyl-CoA synthetase long-chain family member 4 (ACSL4), an enzyme that promotes biosynthesis of phospholipid hydroperoxides, along with uterine epithelial GPX4 deletion, preserves reproductive capacity. This study reveals the pernicious impact of unbalanced redox signaling on embryo implantation and suggests the obliteration of lipid peroxides as a possible therapeutic approach to prevent implantation defects.

Indexed as

Lipid PeroxidesUterusEmbryo ImplantationEpitheliumFemaleHumansLipid PeroxidationPregnancyLipid Peroxidesembryo implantationfemale fertilityGPX4lipid peroxidationuterine receptivity

Identifiers

PMID38044324
PMCPMC10811501
OpenAlexW4389290615

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.