| Autor: |
Liu, Yi-Chen, Gong, Yi-Ting, Sun, Qing-Yan, Wang, Bei, Yan, Yue, Chen, Yi-Xu, Zhang, Li-Jun, Zhang, Wei-Dong, Luan, Xin |
| Předmět: |
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| Zdroj: |
Cellular Oncology (2211-3428); Feb2024, Vol. 47 Issue 1, p19-35, 17p |
| Abstrakt: |
Background: Ferroptosis, a newly form of regulated cell death (RCD), is characterized by iron dyshomeostasis and unrestricted lipid peroxidation. Emerging evidence depicts a pivotal role for ferroptosis in driving some pathological processes, especially in cancer. Triggering ferroptosis can suppress tumor growth and induce an anti-tumor immune response, denoting the therapeutic promises for targeting ferroptosis in the management of cancer. As an autophagic phenomenon, ferritinophagy is critical to induce ferroptosis by degradation of ferritin to release intracellular free iron. Recently, a great deal of effort has gone into designing and developing anti-cancer strategies based on targeting ferritinophagy to induce ferroptosis. Conclusion: This review delineates the regulatory mechanism of ferritinophagy firstly and summarizes the role of ferritinophagy-induced ferroptosis in cancer. Moreover, the strategies targeting ferritinophagy to induce ferroptosis are highlighted to unveil the therapeutic value of ferritinophagy as a target to manage cancer. Finally, the future research directions on how to cope with the challenges in developing ferritinophagy promoters into clinical therapeutics are discussed. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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