Necroptosis: a regulated cell death pathway and potential therapeutic target in neurodegenerative disorders
DOI:
https://doi.org/10.59736/IJP.24.03.1146Keywords:
Necroptosis, RIPK1, RIPK3, MLKL, Neuroinflammation, Therapeutic TargetsAbstract
Necroptosis is a programmed cell death characterized by damage to the plasma membrane, secretion of cytoplasmic content, and inflammation induction. Recent findings suggest that the pathogenesis of tissue injuries associated with dysregulation of necroptosis signaling contributes significantly to the onset of neurodegenerative diseases. The canonical necroptosis signaling pathway includes the activation of receptor-interacting serine/threonine-protein kinases 1 and 3 (RIPK1 and RIPK3) and the function of the mixed lineage kinase domain-like protein (MLKL). The dysregulation of such signaling results in neuronal and glial injuries and increased inflammation. Abnormalities of the necroptosis signaling have been demonstrated in many neurodegenerative diseases, including Alzheimer’s disease, Parkinson’s disease, amyotrophic lateral sclerosis, and multiple sclerosis. The manipulation of the RIPK1, RIPK3, and MLKL expression using pharmaceutical agents has shown positive results in the treatment of such diseases. However, the importance of necroptosis in physiological processes and protection against infections cannot be overestimated. This editorial emphasizes the relevance of necroptosis in neurodegenerative disease pathology and its potential as a pharmacological target. Difficulties associated with translating research into clinical application in the realm of pharmaceutical interventions are also discussed. Additional research in regulation of signaling pathways, disease mechanisms, timing, and safety of the necroptosis inhibitors may lead to novel treatments for neurodegenerative diseases.
References
REFERENCES
Zhu T, Wu B-W. Recognition of necroptosis: From molecular mechanisms to detection methods. Biomedicine & Pharmacotherapy. 2024;178:117196.
Tang J, Zhuang Y, Zhang Y, Hu H, Wang H, Xu H, et al. Necroptosis in cancer: insight from epigenetic, post-transcriptional and post-translational modifications. Journal of hematology & oncology. 2025;18(1):77.
Chaouhan HS, Vinod C, Mahapatra N, Yu S-H, Wang I-K, Chen K-B, et al. Necroptosis: A Pathogenic Negotiator in Human Diseases. International Journal of Molecular Sciences. 2022;23(21):12714.
Morgan MJ, Kim Y-S. Roles of RIPK3 in necroptosis, cell signaling, and disease. Experimental & Molecular Medicine. 2022;54(10):1695-704.
Mahnoor, Jahan S, Elahi L, Zakria M, Rabia, Ikram M, Ullah N. Alpha-Linolenic Acid for Mitigating Neuroinflammation and Dopaminergic Neuronal Loss in Parkinson’s Disease: Insights From In Vivo and In Silico Studies. Clinical and Experimental Pharmacology and Physiology. 2025;52:e70043
Jahan S, Ikram M, Khan Z. Beyond the Brain: The Peripheral Revolution in Neurodegenerative Diseases. Int J Pathol. 2026;24(2):80–82. https://doi.org/10.59736/IJP.24.02.1100
Ye K, Chen Z, Xu Y. The double-edged functions of necroptosis. Cell death & disease. 2023;14(2):163.
Balusu S, De Strooper B. The necroptosis cell death pathway drives neurodegeneration in Alzheimer’s disease. Acta Neuropathologica. 2024;147(1):96.
Yang M, Chen W, He L, Liu D, Zhao L, Wang X. A Glimpse of necroptosis and diseases. Biomedicine & Pharmacotherapy. 2022;156:113925.
Kang K, Park C, Chan FK-M. Necroptosis at a glance. Journal of Cell Science. 2022;135(17).
Kang A, Qiao Y, Pan S, Yan F, Chen H, Bai Y. From RIPK1 to Necroptosis: Pathogenic Mechanisms in Neurodegenerative Diseases. Neurochemical Research. 2025;50(3):194.
Jahan S, Ikram M, Siraj S, Ullah S, Zakria M, Ahmad N. Emodin, a Potent Anthraquinone Mitigates MPTP-Induced Parkinson’s Disease Pathology by Regulating Nrf2 and Its Downstream Targets: In Silico and In Vivo Approach. Molecular Neurobiology. 2025;62:8103–8120
Downloads
Published
Issue
Section
License
Copyright (c) 2026 Husnain Qadir, Muhammad Ikram, Sarwat Jahan

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Readers may “Share-copy and redistribute the material in any medium or format” and “Adapt-remix, transform, and build upon the material”. The readers must give appropriate credit to the source of the material and indicate if changes were made to the material. Readers may not use the material for commercial purpose. The readers may not apply legal terms or technological measures that legally restrict others from doing anything the license permits.
