{"title":"Battling pain from osteoarthritis: causing novel cell death.","authors":"Yuheng Zhang, Huaqiang Tao, Liyuan Zhang, Xueyan Li, Yi Shi, Wen Sun, Wenlong Chen, Yuhu Zhao, Liangliang Wang, Xing Yang, Chengyong Gu","doi":"10.3724/abbs.2024189","DOIUrl":null,"url":null,"abstract":"<p><p>Osteoarthritis (OA) is a significant contributor to pain and disability worldwide. Pain is the main complaint of OA patients attending the clinic and has a large impact on their quality of life and economic standards. However, existing treatments for OA-related pain have not been shown to achieve good relief. The main focus is on preventing and slowing the progression of OA so that the problem of OA pain can be resolved. Pain caused by OA is complex, with the nature, location, duration, and intensity of pain changing as the disease progresses. Previous research has highlighted the role of various forms of cell death, such as apoptosis and necrosis, in the progression of pain in OA. Emerging studies have identified additional forms of novel cell death, such as pyroptosis, ferroptosis, and necroptosis that are linked to pain in OA. Different types of cell death contribute to tissue damage in OA by impacting inflammatory responses, reactive oxygen species (ROS) production, and calcium ion levels, ultimately leading to the development of pain. Evidence suggests that targeting novel types of cell death could help alleviate pain in OA patients. This review delves into the complex mechanisms of OA pain, explores the relationship between different modes of novel cell death and pain, and proposes novel cell death as a viable strategy for the treatment of these conditions, with the goal of providing scientific references for the development of future OA pain treatments and drugs.</p>","PeriodicalId":6978,"journal":{"name":"Acta biochimica et biophysica Sinica","volume":null,"pages":null},"PeriodicalIF":3.3000,"publicationDate":"2024-10-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta biochimica et biophysica Sinica","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3724/abbs.2024189","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Osteoarthritis (OA) is a significant contributor to pain and disability worldwide. Pain is the main complaint of OA patients attending the clinic and has a large impact on their quality of life and economic standards. However, existing treatments for OA-related pain have not been shown to achieve good relief. The main focus is on preventing and slowing the progression of OA so that the problem of OA pain can be resolved. Pain caused by OA is complex, with the nature, location, duration, and intensity of pain changing as the disease progresses. Previous research has highlighted the role of various forms of cell death, such as apoptosis and necrosis, in the progression of pain in OA. Emerging studies have identified additional forms of novel cell death, such as pyroptosis, ferroptosis, and necroptosis that are linked to pain in OA. Different types of cell death contribute to tissue damage in OA by impacting inflammatory responses, reactive oxygen species (ROS) production, and calcium ion levels, ultimately leading to the development of pain. Evidence suggests that targeting novel types of cell death could help alleviate pain in OA patients. This review delves into the complex mechanisms of OA pain, explores the relationship between different modes of novel cell death and pain, and proposes novel cell death as a viable strategy for the treatment of these conditions, with the goal of providing scientific references for the development of future OA pain treatments and drugs.
骨关节炎(OA)是导致全球疼痛和残疾的一个重要因素。疼痛是骨关节炎患者就诊的主要诉求,对他们的生活质量和经济水平有很大影响。然而,现有的治疗 OA 相关疼痛的方法并未显示出良好的缓解效果。目前的主要重点是预防和减缓 OA 的发展,从而解决 OA 疼痛问题。OA 引起的疼痛是复杂的,疼痛的性质、部位、持续时间和强度会随着疾病的进展而变化。以往的研究强调了细胞凋亡和坏死等各种形式的细胞死亡在 OA 疼痛进展中的作用。新近的研究发现了更多形式的新型细胞死亡,如热凋亡、铁凋亡和坏死,它们与 OA 疼痛有关。不同类型的细胞死亡会影响炎症反应、活性氧(ROS)生成和钙离子水平,从而造成 OA 组织损伤,最终导致疼痛的发生。有证据表明,针对新型细胞死亡有助于减轻 OA 患者的疼痛。本综述深入探讨了 OA 疼痛的复杂机制,探讨了新型细胞死亡的不同模式与疼痛之间的关系,并提出将新型细胞死亡作为治疗这些病症的可行策略,目的是为开发未来的 OA 疼痛治疗方法和药物提供科学参考。
期刊介绍:
Acta Biochimica et Biophysica Sinica (ABBS) is an internationally peer-reviewed journal sponsored by the Shanghai Institute of Biochemistry and Cell Biology (CAS). ABBS aims to publish original research articles and review articles in diverse fields of biochemical research including Protein Science, Nucleic Acids, Molecular Biology, Cell Biology, Biophysics, Immunology, and Signal Transduction, etc.