微泡
外体
GPX4
癌症研究
脂质过氧化
诱导剂
癌细胞
癌症
生物
医学
小RNA
氧化应激
谷胱甘肽
生物化学
内科学
基因
酶
谷胱甘肽过氧化物酶
作者
Yixin Shi,Bingrun Qiu,Linyang Huang,Jie Lin,Yiling Li,Yiting Ze,Cheng‐Long Huang,Yang Yao
出处
期刊:PeerJ
[PeerJ]
日期:2022-04-26
卷期号:10: e13238-e13238
被引量:6
摘要
Research on the biological role of exosomes is rapidly developing, and recent evidence suggests that exosomal effects involve ferroptosis. Exosomes derived from different tissues inhibit ferroptosis, which increases tumour cell chemoresistance. Therefore, exosome-mediated regulation of ferroptosis may be leveraged to design anticancer drugs. This review discusses three pathways of exosome-mediated inhibition of ferroptosis: (1) the Fenton reaction; (2) the ferroptosis defence system, including the Xc-GSH-GPX4 axis and the FSP1/CoQ10/NAD(P)H axis; and (3) lipid peroxidation. We also summarize three recent approaches for combining exosomes and ferroptosis in oncology therapy: (1) promoting exosome-inhibited ferroptosis to enhance chemotherapy; (2) encapsulating exosomes with ferroptosis inducers to inhibit cancers; and (3) developing therapies that combine exosomal inhibitors and ferroptosis inducers. This review will contribute toward establishing effective cancer therapies.
科研通智能强力驱动
Strongly Powered by AbleSci AI