端粒酶mRNA治疗保护人体皮肤免受辐射诱导的DNA损伤。

IF 12 1区 医学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Shuang Li,David F Chang,Karem A Court,Thi Kim Cuc Nguyen,Vrutant V Shah,Elisa Morales,Jack Carrier,Anjana Tiwari,Andrew T Ludlow,Kristopher W Brannan,Aldona J Spiegel,Maham Rahimi,Jeffrey D Friedman,Elizabeth Olmsted-Davis,Biana Godin,Anahita Mojiri,John P Cooke
{"title":"端粒酶mRNA治疗保护人体皮肤免受辐射诱导的DNA损伤。","authors":"Shuang Li,David F Chang,Karem A Court,Thi Kim Cuc Nguyen,Vrutant V Shah,Elisa Morales,Jack Carrier,Anjana Tiwari,Andrew T Ludlow,Kristopher W Brannan,Aldona J Spiegel,Maham Rahimi,Jeffrey D Friedman,Elizabeth Olmsted-Davis,Biana Godin,Anahita Mojiri,John P Cooke","doi":"10.1016/j.ymthe.2025.09.029","DOIUrl":null,"url":null,"abstract":"Radiation therapy, while effective against cancer, often causes collateral damage to surrounding healthy tissues, leading to DNA damage that can precipitate genomic instability and cancer. Despite the enormity of the problem, there is currently no FDA-approved agent to prevent or treat skin damage caused by ionizing radiation. In the current study, ionizing radiation induced dose-dependent genomic and mitochondrial DNA damage, leading to apoptosis in primary cutaneous cells. Prior treatment with mRNA encoding telomerase reverse transcriptase (TERT) substantially reduced radiation induced DNA damage in human primary skin cells and tissues. Mechanistically, TERT mRNA pretreatment enhances DNA repair through the homologous recombination pathway, reduces mitochondrial ROS, and decreases apoptosis without extending telomere length during the experimental period, suggesting a non-canonical function of TERT to accelerate cellular recovery from radiation. These findings highlight a potential therapeutic approach for preventing radiation-induced skin injury.","PeriodicalId":19020,"journal":{"name":"Molecular Therapy","volume":"22 1","pages":""},"PeriodicalIF":12.0000,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Telomerase mRNA Therapy Protects Human Skin Against Radiation-Induced DNA Damage.\",\"authors\":\"Shuang Li,David F Chang,Karem A Court,Thi Kim Cuc Nguyen,Vrutant V Shah,Elisa Morales,Jack Carrier,Anjana Tiwari,Andrew T Ludlow,Kristopher W Brannan,Aldona J Spiegel,Maham Rahimi,Jeffrey D Friedman,Elizabeth Olmsted-Davis,Biana Godin,Anahita Mojiri,John P Cooke\",\"doi\":\"10.1016/j.ymthe.2025.09.029\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Radiation therapy, while effective against cancer, often causes collateral damage to surrounding healthy tissues, leading to DNA damage that can precipitate genomic instability and cancer. Despite the enormity of the problem, there is currently no FDA-approved agent to prevent or treat skin damage caused by ionizing radiation. In the current study, ionizing radiation induced dose-dependent genomic and mitochondrial DNA damage, leading to apoptosis in primary cutaneous cells. Prior treatment with mRNA encoding telomerase reverse transcriptase (TERT) substantially reduced radiation induced DNA damage in human primary skin cells and tissues. Mechanistically, TERT mRNA pretreatment enhances DNA repair through the homologous recombination pathway, reduces mitochondrial ROS, and decreases apoptosis without extending telomere length during the experimental period, suggesting a non-canonical function of TERT to accelerate cellular recovery from radiation. These findings highlight a potential therapeutic approach for preventing radiation-induced skin injury.\",\"PeriodicalId\":19020,\"journal\":{\"name\":\"Molecular Therapy\",\"volume\":\"22 1\",\"pages\":\"\"},\"PeriodicalIF\":12.0000,\"publicationDate\":\"2025-09-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular Therapy\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.ymthe.2025.09.029\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular Therapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.ymthe.2025.09.029","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

放射治疗虽然对癌症有效,但往往会对周围的健康组织造成附带损害,导致DNA损伤,从而导致基因组不稳定和癌症。尽管这个问题很严重,但目前还没有fda批准的药物来预防或治疗电离辐射造成的皮肤损伤。在目前的研究中,电离辐射诱导剂量依赖性基因组和线粒体DNA损伤,导致原代皮肤细胞凋亡。先前用mRNA编码端粒酶逆转录酶(TERT)治疗可显著降低辐射诱导的人类原代皮肤细胞和组织的DNA损伤。在机制上,TERT mRNA预处理通过同源重组途径增强DNA修复,减少线粒体ROS,在不延长端粒长度的情况下减少细胞凋亡,表明TERT具有加速辐射后细胞恢复的非规范功能。这些发现强调了预防辐射引起的皮肤损伤的潜在治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Telomerase mRNA Therapy Protects Human Skin Against Radiation-Induced DNA Damage.
Radiation therapy, while effective against cancer, often causes collateral damage to surrounding healthy tissues, leading to DNA damage that can precipitate genomic instability and cancer. Despite the enormity of the problem, there is currently no FDA-approved agent to prevent or treat skin damage caused by ionizing radiation. In the current study, ionizing radiation induced dose-dependent genomic and mitochondrial DNA damage, leading to apoptosis in primary cutaneous cells. Prior treatment with mRNA encoding telomerase reverse transcriptase (TERT) substantially reduced radiation induced DNA damage in human primary skin cells and tissues. Mechanistically, TERT mRNA pretreatment enhances DNA repair through the homologous recombination pathway, reduces mitochondrial ROS, and decreases apoptosis without extending telomere length during the experimental period, suggesting a non-canonical function of TERT to accelerate cellular recovery from radiation. These findings highlight a potential therapeutic approach for preventing radiation-induced skin injury.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Molecular Therapy
Molecular Therapy 医学-生物工程与应用微生物
CiteScore
19.20
自引率
3.20%
发文量
357
审稿时长
3 months
期刊介绍: Molecular Therapy is the leading journal for research in gene transfer, vector development, stem cell manipulation, and therapeutic interventions. It covers a broad spectrum of topics including genetic and acquired disease correction, vaccine development, pre-clinical validation, safety/efficacy studies, and clinical trials. With a focus on advancing genetics, medicine, and biotechnology, Molecular Therapy publishes peer-reviewed research, reviews, and commentaries to showcase the latest advancements in the field. With an impressive impact factor of 12.4 in 2022, it continues to attract top-tier contributions.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信