Evidence map›Paper›PMID 39966422›Full record

ArticleCell death discovery2025

Decreased miR-128-3p in serum exosomes from polycystic ovary syndrome induces ferroptosis in granulosa cells via the p38/JNK/SLC7A11 axis through targeting CSF1.

Yanqiu Lv, Shengzhong Han, Fuliang Sun, Yuyang Zhang, Xinglin Qu, Hao Li, Weiyu Gu, Qinglong Xu, Shunfa Yao, Xuan Chen and 1 more

Abstract read
In one paragraph

Article in Cell death discovery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 3 pooled it
–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

12 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. MicroRNA Crossroads in PCOS and Endometriosis.Reproductive sciences (Thousand Oaks, Calif.) · 2026
    Review
  11. Review
  12. Article
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

11 authors.

Yanqiu Lv *Department of Animal Science, College of Agriculture, Yanbian University, Jilin, China.
Shengzhong Han *Department of Animal Science, College of Agriculture, Yanbian University, Jilin, China.
Fuliang SunDepartment of Animal Science, College of Agriculture, Yanbian University, Jilin, China.
Yuyang ZhangDepartment of Animal Science, College of Agriculture, Yanbian University, Jilin, China.
Xinglin QuDepartment of Animal Science, College of Agriculture, Yanbian University, Jilin, China.
Hao LiDepartment of Animal Science, College of Agriculture, Yanbian University, Jilin, China.
Weiyu GuDepartment of Animal Science, College of Agriculture, Yanbian University, Jilin, China.
Qinglong XuDepartment of Animal Science, College of Agriculture, Yanbian University, Jilin, China.
Shunfa YaoDepartment of Animal Science, College of Agriculture, Yanbian University, Jilin, China.
Xuan ChenDepartment of Animal Science, College of Agriculture, Yanbian University, Jilin, China. 0000008862@ybu.edu.cn.
Yi JinDepartment of Animal Science, College of Agriculture, Yanbian University, Jilin, China. yijin@ybu.edu.cn.ORCID http://orcid.org/0000-0003-1794-7017

Funding

National Natural Science Foundation of China (National Science Foundation of China) No. 31960659National Natural Science Foundation of China (National Science Foundation of China) No. 32360834
6 · The paper itself

Abstract

Increasing evidence suggests that non-coding small RNAs (miRNAs) carried by exosomes (EXOs) play important roles in the development and treatment of polycystic ovary syndrome (PCOS). In this study, we demonstrate that PCOS mouse serum-derived EXOs promote granulosa cells (GCs) ferroptosis, and induce the occurrence of a PCOS-like phenotype in vivo. Notably, EXO miRNA sequencing combined with in vitro gain- and loss-of-function assays revealed that miR-128-3p, which is absent in the serum-derived EXOs of mice with PCOS, regulates lipid peroxidation and GC sensitivity to ferroptosis inducers. Mechanistically, overexpression of CSF1, a direct target of miR-128-3p, reversed the anti-ferroptotic effect of miR-128-3p. Conversely, ferroptosis induction was mitigated in CSF1-downregulated GCs. Furthermore, we demonstrated that miR-128-3p inhibition activates the p38/JNK pathway via CSF1, leading to NRF2-mediated down-regulation of SLC7A11 transcription, which triggers GC iron overload. Moreover, intrathecal miR-128-3p AgomiR injection into mouse ovaries ameliorated PCOS-like characteristics and restored fertility in letrozole-induced mice. The study reveals the pathological mechanisms of PCOS based on circulating EXOs and provides the first evidence of the roles of miR-128-3p and CSF1 in ovarian GCs. This discovery is expected to provide promising therapeutic targets for the treatment of PCOS.

Identifiers

PMID39966422
PMCPMC11836375

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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.