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}
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.
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.