Radiation interactions with biological systems

References

• Amorati R, Baschieri A, Morroni G, Gambino R, Valgimigli L. 2016. Peroxyl radical reactions in water solution: a gym for proton-coupled electron-transfer theories. Chemistry. 22:7924–7934.
   PubMed Web of Science ®Google Scholar
• Antipova VN, Malakhova LV, Bezlepkin VG. 2011. Detection of large deletions of mitochondrial DNA in tissues of mice exposed to X-rays. Biofizika. 56:439–445.
   PubMedGoogle Scholar
• Attri P, Kim YH, Park DH, Park JH, Hong YJ, Uhm HS, Kim K-N, Fridman A, Eun Ha Choi EH. 2015. Generation mechanism of hydroxyl radical species and its lifetime prediction during the plasma-initiated ultraviolet (UV) photolysis. Sci Rep. 5:1–8.
   Web of Science ®Google Scholar
• Baraibar MA, Liu L, Ahmed EK, Friguet B. 2012. Protein oxidative damage at the crossroads of cellular senescence, aging, and age-related diseases. Oxidat Med Cellul Longev. 2012:8.
   Web of Science ®Google Scholar
• Bleier L, Wittig I, Heide H, Steger M, Brandt U, Dröse S. 2015. Generator-specific targets of mitochondrial reactive oxygen species. Free Radic Biol Med. 78:1–10.
   PubMed Web of Science ®Google Scholar
• Bronzini I, Aresu L, Paganin M, Marchioretto L, Comazzi S, Cian F, Riondato F, Marconato L, Martini V, Te Kronnie G. 2016. DNA methylation and targeted sequencing of methyltransferases family genes in canine acute myeloid leukaemia, modelling human myeloid leukaemia. Vet Comp Oncol. [Epub ahead of print]. doi: 10.1111/vco.12231.
   PubMedGoogle Scholar
• Brooks AL. 2005. Paradigm shifts in radiation biology: their impact on intervention for radiation-induced disease. Radiat Res. 164:454–461.
   PubMed Web of Science ®Google Scholar
• Bulteau AL, Ikeda-Saito M, Szweda LI. 2003. Redox-dependent modulation of aconitase activity in intact mitochondria. Biochemistry. 42:14846–14855.
   PubMed Web of Science ®Google Scholar
• Buonanno M, De Toledo SM, Pain D, Azzam EI. 2011. Long-term consequences of radiation-induced bystander effects depend on radiation quality and dose and correlate with oxidative stress. Radiat Res. 175:405–415.
   PubMed Web of Science ®Google Scholar
• Cadet J, Douki T, Ravanat JL. 2011. Measurement of oxidatively generated base damage in cellular DNA. Mutat Res. 711:3–12.
   PubMed Web of Science ®Google Scholar
• Cassano P, Petrie SR, Hamblin MR, Henderson TA, Iosifescu DV. 2016. Review of transcranial photobiomodulation for major depressive disorder: targeting brain metabolism, inflammation, oxidative stress, and neurogenesis. Neurophotonics. 3:031404.
   PubMed Web of Science ®Google Scholar
• Chaudhry MA, Omaruddin RA. 2011. Mitochondrial gene expression in directly irradiated and nonirradiated bystander cells. Cancer Biother Radiopharm. 26:657–663.
   PubMed Web of Science ®Google Scholar
• Cheng X, Ivessa AS. 2010. The migration of mitochondrial DNA fragments to the nucleus affects the chronological aging process of Saccharomyces cerevisiae. Aging Cell. 9:919–923.
   PubMed Web of Science ®Google Scholar
• Chiu HW, Lin W, Ho SY, Wang YJ. 2011. Synergistic effects of arsenic trioxide and radiation in osteosarcoma cells through the induction of both autophagy and apoptosis. Radiat Res. 175:547–560.
   PubMed Web of Science ®Google Scholar
• Claus G, Cowan G, Eidelman SD, Stroh T. 2005. Astroparticle physics. Berlin Heidelberg: Springer; p. 109. Available from: http://www2.fisica.unlp.edu.ar/blogs/tgc/Grupen%20C.%20Astroparticle%20Physics%20(Springer%202005)(448s)_PGrc_.pdf
   Google Scholar
• de Toledo SM, Asaad N, Venkatachalam P, Li L, Howell RW, Spitz DR, Azzam EI. 2006. Adaptive responses to low-dose/low-dose-rate gamma rays in normal human fibroblasts: the role of growth architecture and oxidative metabolism. Radiat Res. 166:849–857.
   PubMed Web of Science ®Google Scholar
• Du C, Gao Z, Venkatesha VA, Kalen AL, Chaudhuri L, Spitz DR, Cullen JJ, Oberley LW, Goswami PC. 2009. Mitochondrial ROS and radiation induced transformation in mouse embryonic fibroblasts. Cancer Biol Therap. 8:1962–1971.
   PubMed Web of Science ®Google Scholar
• Eriksson P, Buratovic S, Fredriksson A, Stenerlöw B, Sundell-Bergman S. 2016. Neonatal exposure to whole body ionizing radiation induces adult neurobehavioural defects: critical period, dose-response effects and strain and sex comparison. Behav Brain Res. 304:11–19.
   PubMed Web of Science ®Google Scholar
• Esch T, Stefano GB, Fricchione GL, Benson H. 2002. Stress-related diseases: a potential role for nitric oxide. Med Sci Monit. 8:103–118.
   Google Scholar
• Fallahi B, Esmaeili A, Beiki D, Oveisgharan S, Noorollahi-Moghaddam H, Erfani M, Tafakhori A, Rohani M, Fard-Esfahani A, Emami-Ardekani A, et al. 2016. Evaluation of (99m)Tc-TRODAT-1 SPECT in the diagnosis of Parkinson’s disease versus other progressive movement disorders. Ann Nucl Med. 30:153–162.
   PubMed Web of Science ®Google Scholar
• Fike JR, Rosi S, Limoli CL. 2009. Neural precursor cells and central nervous system radiation sensitivity. Semin Radiat Oncol. 19:122–132.
   PubMed Web of Science ®Google Scholar
• Finkel T. 2001. Reactive oxygen species and signal transduction. IUBMB Life. 52:3–6.
   PubMed Web of Science ®Google Scholar
• Gaziev AI, Shaikhaev GO. 2007. Ionizing radiation can activate the insertion of mitochondrial DNA fragments in the nuclear genome. Radiatsionnaia Biologiia, Radioecologiia/Rossiiskaia Akademiia Nauk. 47:673–683.
   PubMedGoogle Scholar
• Georgakilas AG, Holt SM, Hair JM, Loftin CW. 2010. Measurement of oxidatively-induced clustered DNA lesions using a novel adaptation of single cell gel electrophoresis (comet assay). Curr Protoc Cell Biol. Chapter 6: Unit 6.11. doi: 10.1002/0471143030.cb0611s49.
   PubMedGoogle Scholar
• Grishko VI, Rachek LI, Spitz DR, Wilson GL, LeDoux SP. 2005. Contribution of mitochondrial DNA repair to cell resistance from oxidative stress. J Biol Chem. 280:8901–8905.
   PubMed Web of Science ®Google Scholar
• Gyurkovska V, Ivanovska N. 2016. Distinct roles of TNF-related apoptosis-inducing ligand (TRAIL) in viral and bacterial infections: from pathogenesis to pathogen clearance. Inflamm Res. 65:427–437.
   PubMed Web of Science ®Google Scholar
• Hall EJ, Giaccia AJ. 2006. Radiobiology for the Radiologist. 6th ed. Philadelphia, PA: Lippincott Williams & Wilkins.
   Google Scholar
• Hanahan D, Weinberg RA. 2011. Hallmarks of cancer: the next generation. Cell. 144:646–674.
   PubMed Web of Science ®Google Scholar
• Jain MR, Li M, Chen W, Liu T, De Toledo SM, Pandey BN, Li H, Rabin BM, Azzam EI. 2011. In vivo space radiation-induced non-targeted responses: late effects on molecular signaling in mitochondria. CMP. 4:106–114.
   Google Scholar
• Kahanda D, Chakrabarti G, Mcwilliams MA, Boothman DA, Slinker JD. 2016. Using DNA devices to track anticancer drug activity. Biosens Bioelectron. 80:647–653.
   PubMed Web of Science ®Google Scholar
• Keszenman DJ, Kolodiuk L, Baulch JE. 2015. DNA damage in cells exhibiting radiation-induced genomic instability. Mutagenesis. 30:451–458.
   PubMed Web of Science ®Google Scholar
• Kim GJ, Fiskum GM, Morgan WF. 2006. A role for mitochondrial dysfunction in perpetuating radiation-induced genomic instability. Cancer Res. 66:10377–10383.
   PubMed Web of Science ®Google Scholar
• Kryston TB, Georgiev AB, Pissis P, Georgakilas AG. 2011. Role of oxidative stress and DNA damage in human carcinogenesis. Mutat Res. 711:193–201.
   PubMed Web of Science ®Google Scholar
• Kubsik A, Klimkiewicz R, Janczewska K, Klimkiewicz P, Jankowska A, Woldańska-Okońska M. 2016. Application of laser radiation and magnetostimulation in therapy of patients with multiple sclerosis. NeuroRehabilitation. 38:183–190.
   PubMed Web of Science ®Google Scholar
• Lee MS. 2016. Role of mitochondrial function in cell death and body metabolism. Front Biosci (Landmark Ed). 21:1233–1244.
   PubMed Web of Science ®Google Scholar
• Lien EC, Lyssiotis CA, Juvekar A, Hu H, Asara JM, Cantley LC, Toker A. 2016. Glutathione biosynthesis is a metabolic vulnerability in PI(3)K/Akt-driven breast cancer. Nat Cell Biol. 18:572–578.
   PubMed Web of Science ®Google Scholar
• Lindahl T. 1993. Instability and decay of the primary structure of DNA. Nature. 362:709–715.
   PubMed Web of Science ®Google Scholar
• Lomonaco SL, Finniss S, Xiang C, Decarvalho A, Umansky F, Kalkanis SN, Mikkelsen T, Brodie C. 2009. The induction of autophagy by gamma-radiation contributes to the radioresistance of glioma stem cells. Int J Cancer. 125:717–722.
   PubMed Web of Science ®Google Scholar
• Lovreglio P, Maffei F, Carrieri M, D’Errico MN, Drago I, Hrelia P, Bartolucci GB, Soleo L. 2014. Evaluation of chromosome aberration and micronucleus frequencies in blood lymphocytes of workers exposed to low concentrations of benzene. Mutat Res Genet Toxicol Environ Mutagen. 770:55–60.
   PubMed Web of Science ®Google Scholar
• Malakhova L, Bezlepkin VG, Antipova V, Ushakova T, Fomenko L, Sirota N, Gaziev AI. 2005. The increase in mitochondrial DNA copy number in the tissues of gamma-irradiated mice. Cell Mol Biol Lett. 10:721–732.
   PubMed Web of Science ®Google Scholar
• Martin OA, Redon CE, Nakamura AJ, Dickey JS, Georgakilas AG, Bonner WM. 2011. Systemic DNA damage related to cancer. Cancer Res. 71:3437–3441.
   PubMed Web of Science ®Google Scholar
• Necz PP, Bakos J. 2014. Photobiological safety of the recently introduced energy efficient household lamps. Int J Occup Med Environ Health. 27:1036–1042.
   PubMed Web of Science ®Google Scholar
• Ngo JK, Pomatto LC, Davies KJ. 2013. Upregulation of the mitochondrial Lon Protease allows adaptation to acute oxidative stress but dysregulation is associated with chronic stress, disease, and aging. Redox Biol. 1:258–264.
   PubMed Web of Science ®Google Scholar
• Nystrom T. 2005. Role of oxidative carbonylation in protein quality control and senescence. EMBO J. 24:1311–1317.
   PubMed Web of Science ®Google Scholar
• Ogura A, Oowada S, Kon Y, Hirayama A, Yasui H, Meike S, Kobayashi S, Kuwabara M, Inanami O. 2009. Redox regulation in radiation-induced cytochrome c release from mitochondria of human lung carcinoma A549 cells. Cancer Lett. 277:64–71.
   PubMed Web of Science ®Google Scholar
• O’Neill P, Wardman P. 2009. Radiation chemistry comes before radiation biology. Int J Radiat Biol. 85:9–25.
   PubMed Web of Science ®Google Scholar
• Østergaard L, Engedal TS, Moreton F, Hansen MB, Wardlaw JM, Dalkara T, Markus HS, Muir KW. 2016. Cerebral small vessel disease: capillary pathways to stroke and cognitive decline. J Cereb Blood Flow Metab. 36:302–325.
   PubMed Web of Science ®Google Scholar
• Parsons PA. 2002. Radiation hormesis: challenging LNT theory via ecological and evolutionary considerations. Health Phys. 82:513–516.
   PubMed Web of Science ®Google Scholar
• Rajendran S, Harrison SH, Thomas RA, Tucker JD. 2011. The role of mitochondria in the radiation-induced bystander effect in human lymphoblastoid cells. Radiat Res. 175:159–171.
   PubMed Web of Science ®Google Scholar
• Royal HD. 2008. Effects of low level radiation – what’s new? Semin Nucl Med. 38:392–402.
   PubMed Web of Science ®Google Scholar
• Sahin E, Colla S, Liesa M, Moslehi J, Muller FL, Guo M, Cooper M, Kotton D, Fabian AJ, Walkey C, et al. 2011. Telomere dysfunction induces metabolic and mitochondrial compromise. Nature. 470:359–365.
   PubMed Web of Science ®Google Scholar
• Sakhuja G. 2016. The provenance of nuclear radioactivity and radiations and its deep developmental impact on the mankind. Int J Innovative Res Sci Technol. 5:234–240.
   Google Scholar
• Sedelnikova OA, Redon CE, Dickey JS, Nakamura AJ, Georgakilas AG, Bonner WM. 2010. Role of oxidatively induced DNA lesions in human pathogenesis. Mutat Res. 704:152–159.
   PubMed Web of Science ®Google Scholar
• Spitz DR, Azzam EI, Li JJ, Gius D. 2004. Metabolic oxidation/reduction reactions and cellular responses to ionizing radiation: a unifying concept in stress response biology. Cancer Metastasis Rev. 23:311–322.
   PubMed Web of Science ®Google Scholar
• Sterniczuk M, Bartels DM. 2016. Source of molecular hydrogen in high-temperature water radiolysis. J Phys Chem A. 120:200–209.
   PubMed Web of Science ®Google Scholar
• Sulli G, Di Micco R, d’Adda di Fagagna F. 2012. Crosstalk between chromatin state and DNA damage response in cellular senescence and cancer. Nat Rev Cancer. 12:709–720.
   PubMed Web of Science ®Google Scholar
• Valerie K, Yacoub A, Hagan MP, Curiel DT, Fisher PB, Grant S, Dent P. 2007. Radiation-induced cell signaling: inside-out and outside-in. Molecul Cancer Therapeut. 6:789–801.
   PubMed Web of Science ®Google Scholar
• Vucic V, Isenovic ER, Adzic M, Ruzdijic S, Radojcic MB. 2006. Effects of gamma-radiation on cell growth, cycle arrest, death, and superoxide dismutase expression by DU 145 human prostate cancer cells. Braz J Med Biol. 39:227–236.
   PubMed Web of Science ®Google Scholar
• Wallett A, Newland K, Foster-Smith E. 2016. Radiation therapy-induced neuro-Sweet disease in a patient with oral squamous cell carcinoma. Australas J Dermatol. [Epub ahead of print]. doi: 10.1111/ajd.12442.
   PubMed Web of Science ®Google Scholar
• Weinberg F, Chandel NS. 2009. Reactive oxygen species-dependent signaling regulates cancer. Cell Mol Life Sci. 66:3663–3673.
   PubMed Web of Science ®Google Scholar
• Werner E, Werb Z. 2002. Integrins engage mitochondrial function for signal transduction by a mechanism dependent on Rho GTPases. J Cell Biol. 158:357–368.
   PubMed Web of Science ®Google Scholar
• Wu C, Parrott AM, Fu C, Liu T, Marino SM, Gladyshev VN, Jain MR, Baykal AT, Li Q, Oka S, et al. 2011. Thioredoxin 1-mediated post-translational modifications: reduction, transnitrosylation, denitrosylation, and related proteomics methodologies. Antioxid Redox Signal. 15:2565–2604.
   PubMed Web of Science ®Google Scholar