ReviewBiological trace element research2026
Research Progress on Ferroptosis Regulation of Female Reproduction.
Review in Biological trace element research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Isorhamnetin-preconditioned MSC-derived exosomes restore ovarian function by inhibiting ferroptosis in chemotherapy-induced POF.Stem cell research & therapy · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
Ferroptosis is a form of iron-regulated cell death that plays a critical role in various aspects of female reproductive system development. These processes include the normal estrous cycle, ovarian formation, follicular maturation, ovulation, and pregnancy, all of which are essential for maintaining reproductive health in female animals. However, excessive iron leads to the accumulation of reactive oxygen species within cells, disrupting intracellular redox balance, inducing mitophagy, membrane rupture, and lipid peroxidation, which can damage tissues and cells, ultimately resulting in ferroptosis. An increasing body of research indicates that ferroptosis is associated with the development of several reproductive disorders, including polycystic ovary syndrome, premature ovarian failure, and spontaneous abortion, among others. Simultaneously, ferroptosis-related pathways and genes also regulate the growth and secretion of granulosa cells, impacting oocyte development, ovarian reserve, early embryo development, and oxidative stress in the placenta, all of which significantly limit the reproductive capacity of female animals. This review summarizes the mechanisms of ferroptosis and its impact on female reproduction, offering new insights on the prevention and treatment of reproductive diseases in females. In this paper, the effects of ferroptosis on reproductive ability were studied from the perspective of germ cells, which provided a new perspective for preventing and improving female reproductive ability from the perspective of ferroptosis.
Indexed as
Identifiers
40921996What Socratic holds
Registered trials
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 Socratic graph.