Proteolytic therapeutic modalities for amyloidoses: Insights into immunotherapy, PROTAC, and photo-oxygenation

IF 6.9 2区 医学 Q1 CLINICAL NEUROLOGY Neurotherapeutics Pub Date : 2025-04-01 Epub Date: 2025-02-11 DOI:10.1016/j.neurot.2025.e00548
Mai Kuriyama , Chu Fan Wang , Tatsuya Nagase , Youhei Sohma , Motomu Kanai , Yukiko Hori , Taisuke Tomita
{"title":"Proteolytic therapeutic modalities for amyloidoses: Insights into immunotherapy, PROTAC, and photo-oxygenation","authors":"Mai Kuriyama ,&nbsp;Chu Fan Wang ,&nbsp;Tatsuya Nagase ,&nbsp;Youhei Sohma ,&nbsp;Motomu Kanai ,&nbsp;Yukiko Hori ,&nbsp;Taisuke Tomita","doi":"10.1016/j.neurot.2025.e00548","DOIUrl":null,"url":null,"abstract":"<div><div>Amyloidoses, which are characterized by abnormal accumulation of amyloid proteins leading to organ dysfunction, represent a major therapeutic challenge. They include neurodegenerative diseases, such as Alzheimer disease (AD), tauopathies and synucleinopathies. Since amyloids are causative factors in these diseases, the importance of proteolytic methods to remove amyloid, such as immunotherapy and Proteolysis Targeting Chimera (PROTAC) technology, has been recognized. Immunotherapy removes target proteins by antibody-mediated reactions and is the most studied method in practical use for the treatment of AD. PROTAC is a small molecule that uses the ubiquitin-proteasome system to degrade intracellular target proteins and has demonstrated efficacy in clinical trials for other diseases. In addition, a new modality called photo-oxygenation has been developed. Photo-oxygenation is a method of selectively adding oxygen to amyloid using a photocatalyst, which is a small molecule compound that is activated by light. Studies both <em>in vitro</em> and <em>in vivo</em> have shown promising results in inhibiting amyloid aggregation and enhancing the clearance of amyloid proteins. In this review, we introduce and discuss these proteolytic modalities, and provide insights into potential future directions for the clinical application in amyloidoses.</div></div>","PeriodicalId":19159,"journal":{"name":"Neurotherapeutics","volume":"22 3","pages":"Article e00548"},"PeriodicalIF":6.9000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurotherapeutics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1878747925000261","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/11 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Amyloidoses, which are characterized by abnormal accumulation of amyloid proteins leading to organ dysfunction, represent a major therapeutic challenge. They include neurodegenerative diseases, such as Alzheimer disease (AD), tauopathies and synucleinopathies. Since amyloids are causative factors in these diseases, the importance of proteolytic methods to remove amyloid, such as immunotherapy and Proteolysis Targeting Chimera (PROTAC) technology, has been recognized. Immunotherapy removes target proteins by antibody-mediated reactions and is the most studied method in practical use for the treatment of AD. PROTAC is a small molecule that uses the ubiquitin-proteasome system to degrade intracellular target proteins and has demonstrated efficacy in clinical trials for other diseases. In addition, a new modality called photo-oxygenation has been developed. Photo-oxygenation is a method of selectively adding oxygen to amyloid using a photocatalyst, which is a small molecule compound that is activated by light. Studies both in vitro and in vivo have shown promising results in inhibiting amyloid aggregation and enhancing the clearance of amyloid proteins. In this review, we introduce and discuss these proteolytic modalities, and provide insights into potential future directions for the clinical application in amyloidoses.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
淀粉样病变的蛋白水解治疗方式:免疫疗法、PROTAC和光氧合的见解。
淀粉样病变,其特征是淀粉样蛋白的异常积累导致器官功能障碍,是一个主要的治疗挑战。它们包括神经退行性疾病,如阿尔茨海默病(AD)、tau病和突触核蛋白病。由于淀粉样蛋白是这些疾病的致病因素,蛋白水解方法去除淀粉样蛋白的重要性,如免疫疗法和靶向嵌合体蛋白水解(PROTAC)技术,已被认识到。免疫疗法通过抗体介导的反应去除靶蛋白,是实际应用中研究最多的治疗AD的方法。PROTAC是一种利用泛素-蛋白酶体系统降解细胞内靶蛋白的小分子药物,在其他疾病的临床试验中已证明有效。此外,还开发了一种称为光氧化的新模式。光氧化是一种使用光催化剂选择性地向淀粉样蛋白添加氧气的方法,光催化剂是一种被光激活的小分子化合物。体外和体内研究都显示出抑制淀粉样蛋白聚集和增强淀粉样蛋白清除的良好结果。在这篇综述中,我们介绍和讨论了这些蛋白水解方式,并对淀粉样变性的临床应用提供了潜在的未来方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Neurotherapeutics
Neurotherapeutics 医学-神经科学
CiteScore
11.00
自引率
3.50%
发文量
154
审稿时长
6-12 weeks
期刊介绍: Neurotherapeutics® is the journal of the American Society for Experimental Neurotherapeutics (ASENT). Each issue provides critical reviews of an important topic relating to the treatment of neurological disorders written by international authorities. The Journal also publishes original research articles in translational neuroscience including descriptions of cutting edge therapies that cross disciplinary lines and represent important contributions to neurotherapeutics for medical practitioners and other researchers in the field. Neurotherapeutics ® delivers a multidisciplinary perspective on the frontiers of translational neuroscience, provides perspectives on current research and practice, and covers social and ethical as well as scientific issues.
期刊最新文献
Is it time to think about chronotherapy in migraine The therapeutic pipeline in migraine: What does the future hold? Overlapping pathways of migraine and the endocannabinoid system: Potential therapeutic targets Non-neuronal targets for migraine therapy Lithium chloride suppresses ferroptosis of induced pluripotent stem cells with ApoE4/E4 from a sporadic Alzheimer's disease patient
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1