دورية أكاديمية

Ferroptosis: a promising candidate for exosome-mediated regulation in different diseases

التفاصيل البيبلوغرافية
العنوان: Ferroptosis: a promising candidate for exosome-mediated regulation in different diseases
المؤلفون: Limin Liu, Yulin Ye, Rui Lin, Tianyu Liu, Sinan Wang, Zelin Feng, Xiaoli Wang, Hailong Cao, Xin Chen, Junming Miao, Yifei Liu, Kui Jiang, Zhibo Han, Zongjin Li, Xiaocang Cao
المصدر: Cell Communication and Signaling, Vol 22, Iss 1, Pp 1-15 (2024)
بيانات النشر: BMC, 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine
LCC:Cytology
مصطلحات موضوعية: Exosomes, Stem cells, Ferroptosis, Therapeutic target, Signalling pathway, Iron metabolism, Medicine, Cytology, QH573-671
الوصف: Abstract Ferroptosis is a newly discovered form of cell death that is featured in a wide range of diseases. Exosome therapy is a promising therapeutic option that has attracted much attention due to its low immunogenicity, low toxicity, and ability to penetrate biological barriers. In addition, emerging evidence indicates that exosomes possess the ability to modulate the progression of diverse diseases by regulating ferroptosis in damaged cells. Hence, the mechanism by which cell-derived and noncellular-derived exosomes target ferroptosis in different diseases through the system Xc−/GSH/GPX4 axis, NAD(P)H/FSP1/CoQ10 axis, iron metabolism pathway and lipid metabolism pathway associated with ferroptosis, as well as its applications in liver disease, neurological diseases, lung injury, heart injury, cancer and other diseases, are summarized here. Additionally, the role of exosome-regulated ferroptosis as an emerging repair mechanism for damaged tissues and cells is also discussed, and this is expected to be a promising treatment direction for various diseases in the future. Video Abstract
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1478-811X
Relation: https://doaj.org/toc/1478-811X
DOI: 10.1186/s12964-023-01369-w
URL الوصول: https://doaj.org/article/473882418c114cca9cc6e9c7d8e78abe
رقم الأكسشن: edsdoj.473882418c114cca9cc6e9c7d8e78abe
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:1478811X
DOI:10.1186/s12964-023-01369-w