Evidence map›Paper›PMID 38656738›Full record

ArticleJournal of assisted reproduction and genetics2024

Follicular fluid-derived exosomal LncRNA LIPE-AS1 modulates steroid metabolism and survival of granulosa cells leading to oocyte maturation arrest in polycystic ovary syndrome.

Li Yu, Chen Wang, Miao Liu, Lingjin Xia, Te Liu, Qi Che, Wei Cai, Xi Dong, Baishen Pan, Beili Wang and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
7.0field-weighted citation impact, top 3% 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

12 citing papers in PubMed, 13 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

12 authors at 5 institutions in 1 country.

Li YuDepartment of Laboratory Medicine, Zhongshan Hospital, Fudan University, No. 111 Yi Xue Yuan Road, Shanghai, 200032, People's Republic of China.
Chen WangDepartment of Laboratory Medicine, Zhongshan Hospital, Fudan University, No. 111 Yi Xue Yuan Road, Shanghai, 200032, People's Republic of China.
Miao LiuReproductive Medicine Center, Zhongshan Hospital, Fudan University, No. 250 Xiao Mu Qiao Road, Shanghai, 200032, People's Republic of China.
Lingjin XiaShanghai Institute for Biomedical and Pharmaceutical Technologies, No. 2140 Xietu Road, Shanghai, 200000, People's Republic of China.
Te LiuShanghai Geriatric Institute of Chinese Medicine, Shanghai University of Traditional Chinese Medicine, No.725 South Wan Ping Road, Shanghai, 200031, People's Republic of China.
Qi CheReproductive Medicine Center, Zhongshan Hospital, Fudan University, No. 250 Xiao Mu Qiao Road, Shanghai, 200032, People's Republic of China.
Wei CaiReproductive Medicine Center, Zhongshan Hospital, Fudan University, No. 250 Xiao Mu Qiao Road, Shanghai, 200032, People's Republic of China.
Xi DongReproductive Medicine Center, Zhongshan Hospital, Fudan University, No. 250 Xiao Mu Qiao Road, Shanghai, 200032, People's Republic of China.
Baishen PanDepartment of Laboratory Medicine, Zhongshan Hospital, Fudan University, No. 111 Yi Xue Yuan Road, Shanghai, 200032, People's Republic of China.
Beili WangDepartment of Laboratory Medicine, Zhongshan Hospital, Fudan University, No. 111 Yi Xue Yuan Road, Shanghai, 200032, People's Republic of China. Wang.beili1@zs-hospital.sh.cn.
Suying LiuReproductive Medicine Center, Zhongshan Hospital, Fudan University, No. 250 Xiao Mu Qiao Road, Shanghai, 200032, People's Republic of China. Liu.suying@zs-hospital.sh.cn.
Wei GuoDepartment of Laboratory Medicine, Zhongshan Hospital, Fudan University, No. 111 Yi Xue Yuan Road, Shanghai, 200032, People's Republic of China. Guo.Wei@zs-hospital.sh.cn.ORCID http://orcid.org/0000-0003-4406-1094
Fudan University · CNShanghai Institute of Pharmaceutical Industry · CNShanghai Medical College of Fudan University · CNShanghai University of Traditional Chinese Medicine · CNZhongshan Hospital · CN

Funding

Constructing project of clinical key disciplines in Shanghai shslczdzk03302Excellent backbone of Zhongshan Hospital affiliated Fudan University 2021ZSGG08Key medical and health projects of Xiamen YDZX20193502000002National Natural Science Foundation of China 81902139National Natural Science Foundation of China 81971345National Natural Science Foundation of China 81972000National Natural Science Foundation of China 82001545National Natural Science Foundation of China 82071643National Natural Science Foundation of China 82172348National Natural Science Foundation of China 82202607Shanghai Baoshan Medical Key Specialty BSZK2023A18Specialized Fund for the clinical researches of Zhongshan Hospital affiliated Fudan University 2020ZSLC54Specialized Fund for the clinical researches of Zhongshan Hospital affiliated Fudan University ZSLCYJ202346
6 · The paper itself

Abstract

objectiveWomen who are of reproductive age can suffer from polycystic ovary syndrome (PCOS), an endocrine disorder. Anovulatory infertility is mostly caused by aberrant follicular development, which is seen in PCOS patients. Due to the dysfunction of reproductive and endocrine function in PCOS patients, assisted reproduction treatment is one of the main means to obtain clinical pregnancy for PCOS patients. Long non-coding RNA (lncRNA) as a group of functional RNA molecules have been found to participate in the regulation of oocyte function, hormone metabolism, and proliferation and apoptosis of granulosa cells. In this study, we investigated the role of lncRNAs in follicular fluid-derived exosomes and the underlying mechanism of lncRNA LIPE-AS1.

methodsWe used RNA sequencing to analyze the lncRNA profiles of follicular fluid-derived exosomes in PCOS patients and controls. RT-qPCR was performed to detect the expression levels of these lncRNAs in control (n = 30) and PCOS (n = 30) FF exosome samples. Furthermore, we validated the performance of lncRNA LIPE-AS1 in oocyte maturation by in vitro maturation (IVM) experiments in mouse and steroid metabolism in granulosa cells.

resultsWe found 501 lncRNAs were exclusively expressed in the control group and another 273 lncRNAs were found to be specifically expressed in the PCOS group. LncRNA LIPE-AS1, highly expressed in PCOS exosomes, was related to a poor oocyte maturation and embryo development in PCOS patients. Reduced number of MII oocytes were observed in the LIPE-AS1 group by in vitro maturation (IVM) experiments in mouse. LIPE-AS1 was also shown to modulate steroid metabolism and granulosa cell proliferation and apoptosis by LIPE-AS1/miR-4306/LHCGR axis.

conclusionThese findings suggested that the increased expression of LIPE-AS1, facilitated by follicular fluid exosomes, had a significant impact on both oocyte maturation and embryo development. We demonstrated the ceRNA mechanism involving LIPE-AS1, miR-4306, and LHCGR as a regulator of hormone production and metabolism. These findings indicate that LIPE-AS1 is essential in PCOS oocyte maturation and revealed a ceRNA network of LIPE-AS1 and provided new information on abnormal steroid metabolism and oocyte development in PCOS.

Indexed as

ExosomesFollicular FluidGranulosa CellsOocytesPolycystic Ovary SyndromeRNA, Long NoncodingAdultAnimalsApoptosisCell ProliferationFemaleHumansIn Vitro Oocyte Maturation TechniquesMiceOogenesisSteroidsRNA, Long NoncodingSteroidsLHCGRLncRNA-LIPE-AS1Oocyte maturationPolycystic ovary syndrome

Identifiers

PMID38656738
PMCPMC11143127
OpenAlexW4395466569

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Registered trials

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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.