Reprint

Ionizing Radiation, Antioxidant Response and Oxidative Damage: Radiomodulators

Edited by
August 2023
322 pages
  • ISBN978-3-0365-8188-0 (Hardback)
  • ISBN978-3-0365-8189-7 (PDF)

This book is a reprint of the Special Issue Ionizing Radiation, Antioxidant Response and Oxidative Damage: Radiomodulators that was published in

Biology & Life Sciences
Summary

Ionizing radiation (IR) exposure can be deleterious for living tissues and eventually lead to illness or even death. DNA breakdown and the overproduction of highly reactive free radicals, reactive oxygen species (ROS) and reactive nitrogen species (RNS) are considered initiators of IR-induced molecular and cellular damages, whereas NO, TGF-β and other pro-inflammatory cytokines are the primary effectors involved in radiation bystander effects (RIBE). Radiomodulators can reduce (radioprotectors and radiomitigators) or increase (radiosensitizers) IR damage. Past world events have highlighted the urgent need to develop predictive biomarkers of the IR absorbed dose and radiation countermeasures to reduce IR damage. Despite the strong economic and scientific efforts over the last decades, at present, drugs for effective protection against lethal IRs remain an unmet need. Moreover, the development of radiosensitizers that selectively increase IR damage in cancer cells but protecting, or at least do not affect, healthy tissues is also of unquestionable importance to improving patient survival and quality of life. It includes contributions that will help to understand the mechanisms involved in radiation-derived cellular responses and damage, the importance of free radical scavengers and antioxidant cellular defenses in preventing harm, and the relevance of the antiinflammatory response to improve recovery. In accordance, the mechanism of action and effectiveness of relevant radiomodulators are described and discussed, and novel clinical models and IR biomarker technologies are presented.

Format
  • Hardback
License
© 2022 by the authors; CC BY-NC-ND license
Keywords
ferulic acid; total body irradiation; bone marrow microenvironment; stem cell senescence; bone marrow injury; reactive oxygen species; antioxidant defense system; planarians; model animal; irradiation; regeneration; radioprotection; radiation; melatonin; nDNA-repair; mtDNA-mutations; oxidation stress; protection; mitigation; H2O2; ATP; MDA; GSH; X-ray radiation; 3T3 fibroblasts; proliferation; apoptosis; cellular stress; senescence; peroxiredoxin 6; Prdx6; radioprotector; pharmacologic ascorbate; vitamin C; pancreatic cancer; Auranofin; thioredoxin; thioredoxin reductase; peroxiredoxin; nuclear and radiological emergencies; radioprotectors; radiomitigators; radionuclide scavengers; radiation biodosimetry; Olea europaea L. cv. Caiazzana; oleacein; ionising radiation; cancer; radiotherapy; normal tissue; radioprotection; radiosensitization; radiomodulation; total body irradiation; proteomic analysis; oxidative modification profiling; serum albumin; amino acid sequences; radiation biomarker; human lactoferrin; acute gamma irradiation; C57Bl/6 mice; survival rate; open field test; spleen; serum homeostasis; leukocytes; stilbenoid; electron paramagnetic resonance (EPR); FT-IR; electron beam radiation; radioresistance; reactive oxygen species; oxidative phosphorylation; oncometabolites; apoptosis; radiation response; bioinformatics; oxidative stress; transcriptomics; radiobiology database; gene signature; ionizing radiation; intestine; mucositis; microbiome; microbiota; dysbiosis; bacterial dietary supplement; radiomitigator; radiation; hyperthermia; cancer; combination therapy; synergistic effect; oxygenation; hypoxia; immune response; planarians; Tameron; antioxidant; regeneration; radioprotection; n/a