Vinita Chauhan, Veronica S Grybas, Devyn Hoopfer, Casey Higginson, Elizabeth A Ainsbury, Omid Azimzadeh, Afshin Beheshti, Steve Blattnig, Marjan Boerma, Sylvain V Costes, Stephen Doty, Christelle Adam-Guillermin, Nobuyuki Hamada, Patricia Hinton, Janice L Huff, Robert Reynolds, Ruth C Wilkins, Scott Wood, Carole L Yauk
{"title":"不良后果途径在空间辐射研究中的应用。","authors":"Vinita Chauhan, Veronica S Grybas, Devyn Hoopfer, Casey Higginson, Elizabeth A Ainsbury, Omid Azimzadeh, Afshin Beheshti, Steve Blattnig, Marjan Boerma, Sylvain V Costes, Stephen Doty, Christelle Adam-Guillermin, Nobuyuki Hamada, Patricia Hinton, Janice L Huff, Robert Reynolds, Ruth C Wilkins, Scott Wood, Carole L Yauk","doi":"10.1002/em.70031","DOIUrl":null,"url":null,"abstract":"<p><p>Long-duration spaceflight exposes astronauts to various stressors that can alter human physiology, potentially causing immediate and long-term health effects. These stressors can damage biomolecules, cells, tissues, and organs, leading to adverse outcomes. Developing adverse outcome pathways (AOPs) relevant to radiation exposure can guide research priorities and inform risk assessments of future space exploration activities. Through expert consultation, we developed an AOP network linking 18 key events (KEs) to four non-cancer outcomes: learning and memory impairment, bone loss, abnormal vascular remodeling, and cataract development. A novel scoping review methodology informed the evidence evaluation and supported causal linkages between two KEs. The AOP network begins with the molecular initiating event (MIE) of energy deposition onto cells, which may trigger oxidative stress and DNA damage. If DNA damage is misrepaired, it could lead to gene mutations or chromosomal aberrations. In cases where these occur in critical cell cycle genes, there is a possibility of uncontrolled cellular proliferation. Persistent KEs may contribute to the activation of tissue-resident cells, suppression of anti-inflammatory processes, and promotion of chronic inflammation. This inflammatory cycle, potentially driven by mitochondrial dysfunction and immune cell activation, could lead to cell death and tissue damage. Over time, this accumulation of damage might contribute to organ-specific adverse outcomes associated with radiation exposure. This AOP network consolidates knowledge across biological levels and identifies gaps in understanding causal relationships. It aims to guide research for space traveler risk models and can also apply to other radiation exposure scenarios, such as in medical or occupational settings.</p>","PeriodicalId":11791,"journal":{"name":"Environmental and Molecular Mutagenesis","volume":" ","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Adverse Outcome Pathways Applied to Space Radiation Research.\",\"authors\":\"Vinita Chauhan, Veronica S Grybas, Devyn Hoopfer, Casey Higginson, Elizabeth A Ainsbury, Omid Azimzadeh, Afshin Beheshti, Steve Blattnig, Marjan Boerma, Sylvain V Costes, Stephen Doty, Christelle Adam-Guillermin, Nobuyuki Hamada, Patricia Hinton, Janice L Huff, Robert Reynolds, Ruth C Wilkins, Scott Wood, Carole L Yauk\",\"doi\":\"10.1002/em.70031\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Long-duration spaceflight exposes astronauts to various stressors that can alter human physiology, potentially causing immediate and long-term health effects. These stressors can damage biomolecules, cells, tissues, and organs, leading to adverse outcomes. Developing adverse outcome pathways (AOPs) relevant to radiation exposure can guide research priorities and inform risk assessments of future space exploration activities. Through expert consultation, we developed an AOP network linking 18 key events (KEs) to four non-cancer outcomes: learning and memory impairment, bone loss, abnormal vascular remodeling, and cataract development. A novel scoping review methodology informed the evidence evaluation and supported causal linkages between two KEs. The AOP network begins with the molecular initiating event (MIE) of energy deposition onto cells, which may trigger oxidative stress and DNA damage. If DNA damage is misrepaired, it could lead to gene mutations or chromosomal aberrations. In cases where these occur in critical cell cycle genes, there is a possibility of uncontrolled cellular proliferation. Persistent KEs may contribute to the activation of tissue-resident cells, suppression of anti-inflammatory processes, and promotion of chronic inflammation. This inflammatory cycle, potentially driven by mitochondrial dysfunction and immune cell activation, could lead to cell death and tissue damage. Over time, this accumulation of damage might contribute to organ-specific adverse outcomes associated with radiation exposure. This AOP network consolidates knowledge across biological levels and identifies gaps in understanding causal relationships. It aims to guide research for space traveler risk models and can also apply to other radiation exposure scenarios, such as in medical or occupational settings.</p>\",\"PeriodicalId\":11791,\"journal\":{\"name\":\"Environmental and Molecular Mutagenesis\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-09-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Environmental and Molecular Mutagenesis\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://doi.org/10.1002/em.70031\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ENVIRONMENTAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental and Molecular Mutagenesis","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1002/em.70031","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
Adverse Outcome Pathways Applied to Space Radiation Research.
Long-duration spaceflight exposes astronauts to various stressors that can alter human physiology, potentially causing immediate and long-term health effects. These stressors can damage biomolecules, cells, tissues, and organs, leading to adverse outcomes. Developing adverse outcome pathways (AOPs) relevant to radiation exposure can guide research priorities and inform risk assessments of future space exploration activities. Through expert consultation, we developed an AOP network linking 18 key events (KEs) to four non-cancer outcomes: learning and memory impairment, bone loss, abnormal vascular remodeling, and cataract development. A novel scoping review methodology informed the evidence evaluation and supported causal linkages between two KEs. The AOP network begins with the molecular initiating event (MIE) of energy deposition onto cells, which may trigger oxidative stress and DNA damage. If DNA damage is misrepaired, it could lead to gene mutations or chromosomal aberrations. In cases where these occur in critical cell cycle genes, there is a possibility of uncontrolled cellular proliferation. Persistent KEs may contribute to the activation of tissue-resident cells, suppression of anti-inflammatory processes, and promotion of chronic inflammation. This inflammatory cycle, potentially driven by mitochondrial dysfunction and immune cell activation, could lead to cell death and tissue damage. Over time, this accumulation of damage might contribute to organ-specific adverse outcomes associated with radiation exposure. This AOP network consolidates knowledge across biological levels and identifies gaps in understanding causal relationships. It aims to guide research for space traveler risk models and can also apply to other radiation exposure scenarios, such as in medical or occupational settings.
期刊介绍:
Environmental and Molecular Mutagenesis publishes original research manuscripts, reviews and commentaries on topics related to six general areas, with an emphasis on subject matter most suited for the readership of EMM as outlined below. The journal is intended for investigators in fields such as molecular biology, biochemistry, microbiology, genetics and epigenetics, genomics and epigenomics, cancer research, neurobiology, heritable mutation, radiation biology, toxicology, and molecular & environmental epidemiology.