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Updated: Jul 24, 2025

Author Spotlight: Tracing the Ferroptotic Signatures and Cell Death Dynamics in Medulloblastoma for Advanced Therapeutics
Published on: March 15, 2024
The Emerging Roles of Ferroptosis in Neonatal Diseases
Wenqian Chen1, Dali Zheng2, Changyi Yang1
1Department of Neonatology, Fujian Maternity and Child Health Hospital, Affiliated Hospital of Fujian Medical University, Fuzhou, People's Republic of China.
Insights
Ferroptosis, a cell death process, impacts newborns due to unique iron and reactive oxygen species metabolism. Targeting ferroptosis offers new treatment avenues for infant diseases like hypoxic-ischemic encephalopathy.
Area of Science:
- Cell Biology
- Neonatal Medicine
- Pathophysiology
Background:
- Ferroptosis is a regulated cell death pathway involving lipid peroxidation and iron metabolism.
- Newborns exhibit unique physiological states, increasing susceptibility to ferroptosis.
- Ferroptosis is implicated in several neonatal diseases, including HIE, BPD, and NEC.
Purpose of the Study:
- To review the molecular mechanisms of ferroptosis.
- To examine iron and reactive oxygen species metabolism in infants.
- To explore the role of ferroptosis in neonatal disorders and potential therapeutic targets.
Main Methods:
- Systematic literature review.
- Analysis of molecular mechanisms of ferroptosis.
- Synthesis of data on infant metabolism and disease pathology.
Main Results:
- Ferroptosis is characterized by lipid peroxidation and iron dysregulation.
- Infant physiology predisposes them to ferroptosis-related damage.
- Ferroptosis is linked to hypoxic-ischemic encephalopathy, bronchopulmonary dysplasia, and necrotizing enterocolitis.
Conclusions:
- Ferroptosis plays a significant role in neonatal disease pathogenesis.
- Understanding ferroptosis mechanisms is crucial for developing novel infant therapies.
- Targeting ferroptosis presents a promising therapeutic strategy for neonatal conditions.
Abstract:
Ferroptosis is a novel type of programmed cell death involved in many diseases' pathological processes. Ferroptosis is characterized by lipid peroxidation, reactive oxygen species accumulation, and iron metabolism disorder. Newborns are susceptible to ferroptosis due to their special physiological state, which is prone to abnormal iron metabolism and the accumulation of reactive oxygen species. Recent studies have linked ferroptosis to a variety of diseases in the neonatal period (including hypoxic-ischemic encephalopathy, bronchopulmonary dysplasia, and necrotizing enterocolitis). Ferroptosis may become an effective target for the treatment of neonatal-related diseases. In this review, the ferroptosis molecular mechanism, metabolism characteristics of iron and reactive oxygen species in infants, the relationship between ferroptosis and common infant disorders, and the treatment of infant diseases targeted for ferroptosis are systematically summarized.
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