Evidence map›Paper›PMID 39044215›Full record

ArticleReproductive biology and endocrinology : RB&E2024

Nur77 improves ovarian function in reproductive aging mice by activating mitophagy and inhibiting apoptosis.

Ying Yao, Bin Wang, Kaihua Yu, Ji Song, Liyan Wang, Xuehong Zhang, Yulan Li

Abstract read
In one paragraph

Article in Reproductive biology and endocrinology : RB&E, 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
–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

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.

  1. Review
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  7. A decline in follicle cell function is a major driver ofbioRxiv : the preprint server for biology · 2026
    Article
  8. Article
  9. Review
  10. Review
  11. Review
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  14. Mechanistic study on the role of multi-pathway autophagy in ovarian aging: literature review.Apoptosis : an international journal on programmed cell death · 2025
    Review
  15. Review
  16. Review
  17. Functional and Genetic Insights into the Role of theAnimals : an open access journal from MDPI · 2025
    Article
  18. Review
  19. 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

7 authors.

Ying Yao *The First School of Clinical Medicine, Lanzhou University, Lanzhou, China.
Bin Wang *Reproductive Medicine Center, The First Hospital of Lanzhou University, Lanzhou, China.
Kaihua YuThe First School of Clinical Medicine, Lanzhou University, Lanzhou, China.
Ji SongReproductive Medicine Center, The First Hospital of Lanzhou University, Lanzhou, China.
Liyan WangReproductive Medicine Center, The First Hospital of Lanzhou University, Lanzhou, China.
Xuehong ZhangReproductive Medicine Center, The First Hospital of Lanzhou University, Lanzhou, China. zhangxueh@lzu.edu.cn.
Yulan LiDepartment of Anesthesiology, The First Hospital of Lanzhou University, No. 1, Donggang West Road, Chengguan District, Lanzhou, Gansu Province, China. liyul@lzu.edu.cn.

Funding

Fund of the First Hospital of Lanzhou University ldyyyn2021-67Lanzhou Chengguan District Science and Technology Plan Project 2023-11-3
6 · The paper itself

Abstract

Reproductive aging not only affects the fertility and physical and mental health of women but also accelerates the aging process of other organs. There is an urgent need newfor novel mechanisms, targets, and drugs to break the vicious cycle of mitochondrial dysfunction, redox imbalance, and germ cell apoptosis associated with ovarian aging. Autophagy, recognized as a longevity mechanism, has recently become a focal point in anti-aging research. Although mitophagy is a type of autophagy, its role and regulatory mechanisms in ovarian aging, particularly in age-related ovarian function decline, remain unclear. Nerve growth factor inducible gene B (Nur77) is an early response gene that can be stimulated by oxidative stress, DNA damage, metabolism, and inflammation. Recent evidence recommends that decreased expression of Nur77 is associated with age-related myocardial fibrosis, renal dysfunction, and Parkinson's disease; however, its association with ovarian aging has not been studied yet. We herein identified Nur77 as a regulator of germ cell senescence, apoptosis, and mitophagy and found that overexpression of Nur77 can activate mitophagy, improve oxidative stress, reduce apoptosis, and ultimately enhance ovarian reserve in aged mice ovaries. Furthermore, we discovered an association between Nur77 and the AKT pathway through String and molecular docking analyses. Experimental confirmation revealed that the AKT/mTOR signaling pathway is involved in the regulation of Nur77 in ovarian function. In conclusion, our results suggest Nur77 as a promising target for preventing and treating ovarian function decline related to reproductive aging.

Indexed as

AgingApoptosisMitophagyNuclear Receptor Subfamily 4, Group A, Member 1OvaryAnimalsFemaleMiceMice, Inbred C57BLOvarian ReserveOxidative StressProto-Oncogene Proteins c-aktReproductionSignal TransductionNr4a1 protein, mouseNuclear Receptor Subfamily 4, Group A, Member 1Proto-Oncogene Proteins c-aktAgingApoptosisGranulosa cellsMitophagyNur77PINK1/Parkin

Identifiers

PMID39044215
PMCPMC11265396

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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.