| Literature DB >> 33714759 |
Xiaowen Wang1, Shichen Xu2, Li Zhang3, Xian Cheng2, Huixin Yu2, Jiandong Bao2, Rongrong Lu4.
Abstract
Anaplastic thyroid cancer (ATC) is a rare but highly lethal disease. So far, there is no available established treatment which can prolong its survival. In this regard, effective therapies are urgently needed. Vitamin C widely serves as an anti-cancer agent. However, the potential effects of vitamin C against thyroid tumorigenesis remained unclear. The present study demonstrated that vitamin C could significantly inhibit ATC cells growth through ferroptosis activation, evidenced by the GPX4 inactivation, ROS accumulation and iron-dependent lipid peroxidation. Our results demonstrated that vitamin C treatment induced ferritinophagy and subsequent degradation of ferritin, leading to the release of free iron. Excessive iron further triggered ROS generation via Fenton reaction. The positive feedback mediated by ROS and iron sustained lipid peroxidation and further resulted in ferroptosis of ATC cells. The better understanding of the anti-cancer mechanisms of vitamin C provides a potential strategy for ATC therapy.Entities:
Keywords: Anaplastic thyroid cancer; Ferritinophagy; Ferroptosis; Reactive oxygen species; Vitamin C
Year: 2021 PMID: 33714759 DOI: 10.1016/j.bbrc.2021.02.126
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575