This updated and expanded volume gives new insights on ferroptosis – an iron-dependent form of non-apoptotic cell death. The collection of chapters discusses the two major pathways through which ferroptosis can occur: the extrinsic or transporter-dependent pathway and the intrinsic or enzyme-regulated pathway.
Readers will gain an understanding of the multiple levels, on which this special cell death is regulated. Hence, the contributions will take a closer look at epigenetic, transcriptional, posttranscriptional and posttranslational layers. Among the described regulators and transcription factors are GPX4, ACSL4 and NFE2L2.
This edited volume collects reviews related to current knowledge on the integrated molecular machinery of ferroptosis, thereby also describing how dysregulated ferroptosis is involved in human diseases.
Mục lục
Chapter 1. Lipid Metabolism and Homeostasis in Ferroptosis.- Chapter 2. Iron Metabolism and Ferroptosis.- Chapter 3. Targeting Epigenetic Regulation of Ferroptosis in Cancer Therapy.- Chapter 4. The Role of Autophagy in Ferroptosis.- Chapter 5. Heat Shock Proteins and HSF1 in Ferroptosis.- Chapter 6. The Ongoing Search for a Biomarker of Ferroptosis.- Chapter 7. p53 and Ferroptosis.- Chapter 8. Ferroptosis in Cardiovascular Disease.- Chapter 9. Understanding Ferroptosis from a Free Radical Perspective.- Chapter 10. The NRF2-anti-ferroptosis Axis in Health and Disease.- Chapter 11. Epigenetic Modification in Ferroptosis.- Chapter 12. Organelle-specific Mechanisms of Ferroptosis.- Chapter 13. Ferroptosis: A Promising Therapeutic Target for Cardiovascular Diseases.- Chapter 14. Ferroptosis in Central Nervous System Hypoxia–Ischemia.- Chapter 15. Involvement of Ferroptosis in Lupus Nephritis.- Chapter 16. Ferroptosis and Infectious Diseases.- Chapter 17. Selenium Metabolic Pathway in Ferroptotic Cell Death.- Chapter 18. Epigenetic and Post-Translational Regulation of Ferroptosis.- Chapter 19. Phospholipid Peroxidation in Health and Disease.- Chapter 20.- PKCβII–ACSL4 Axis Triggers Ferroptosis and Its Potential Implication in Ferroptosis-Related Diseases.- Chapter 21. Cancer Treatment with Ferroptosis by a Combination of Iron Nanoparticles and Gene Therapy.- Chapter 22. Inhibitors of Oxytosis/Ferroptosis: A New Class of Therapeutics for Alzheimer’s Disease.
Giới thiệu về tác giả
Daolin Tang
Dr Tang’s work chiefly focuses on designing and conducting molecular, cellular, and animal studies to investigate the mechanisms of damage-associated molecular pattern molecule (DAMP) release and activity in autophagy and cell death, and to evaluate novel drug candidates for the treatment of various inflammatory diseases, including cancer. His past contributions to biomedical science include the initial description of the role of high-mobility group box 1 (HMGB1), a classical DAMP, in autophagy. His recent contributions to DAMP biology include the identification of a novel function and activity of HMGB1 in infection and sterile inflammation. More recently, he has also identified a number of regulators of necroptosis, ferroptosis, pyroptosis, and alkaliptosis. In summary, Dr Tang is an outstanding investigator with a proven track record of innovation and achievement in the fields of DAMP, autophagy, and cell death.
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