참고문헌
- Jo, H., & Ban, C. (2016). Aptamer-nanoparticle complexes as powerful diagnostic and therapeutic tools. Exp Mol Med., 48(5), e230. DOI : 10.1038/emm.2016.44.
- Hosseinimehr, S. J. (2007). Trends in the development of radioprotective agents. Drug Discov Today, 12(19-20), 794-805 DOI : 10.1016/j.drudis.2007.07.017
- van der Veen, S. J. et al. (2015). ACE inhibition attenuates radiation-induced cardiopulmonary damag. Radiother Oncol, 114(1), 96-103. DOI : 10.1016/j.radonc.2014.11.017.
- Gultekin, F. A. et al. (2013). Effects of ozone oxidative preconditioning on radiation-induced organ damage in rats. Eur J Cancer., 48(14), 2117-2124. DOI : 10.1093/jrr/rrs073
- Prasad, K N., Cole, W. C., Kumar, B., & Prasad, K. C. (2002). Pros and cons of antioxidant use during radiation therapy. Cancer Treat Rev, 28(2), 79-91. DOI : 10.1053/ctrv.2002.0260
- Sharygin, V. L., Pulatova, M. K., Shliakova, T. G., Mitrokhin, Y. I., & Todorov, I. N. (2005). Activation of Deoxyribonucleotide Synthesis by Radioprotectants and Antioxidants as a Key Stage in Formation of Body Resistance to DNA-Damaging Factors. Izv Akad Nauk Ser Biol, (4), 401-422. PMID: 16212261.
- Nemavarkar, P. S., Chourasia, B. K., & Pasupathy, K. (2004). Detection of γ-Irradiation Induced DNA Damage and Radioprotection of Compounds in Yeast Using Comet Assay. J Radiat Res., 45(2), 169-174. DOI : 10.1269/jrr.45.169
- Kasai, H., Crain, P. F., Kuchino, Y., Nishimura, S., Ootsuyama, A., & Tanooka, H. (1986). Formation of 8-hydroxyguanine moiety in cellular DNA by agents producing oxygen radicals and evidence for its repair. Carcinogenesis, 7(11), 1849-1851. DOI: 10.1093/carcin/7.11.1849
- Vozenin-Brotons, M. C., Milliat, F., Linard, C., Strup, C., Francois, A., Sabourin, J. C., ... & Mathe, D. (2004). Gene expression profile in human late radiation enteritis obtained by high-density cDNA array hybridization. Radiation Research, 161(3), 299-311. DOI : 10.1667/rr3128
- Y. R. Seo, M. R. Kelley, M. L. Smith. (2002). Selenomethionine regulation of p53 by a ref1-dependent redox mechanism. Proc Natl Acad Sci U S A, 99(22), 14548-14553. DOI : 10.1073/pnas.212319799
- L. J. Egan, L. Eckmann, F. R. Greten, S. Chae, Z. Li, G. M. Myhre, S. Robine, M. Karin, M. Kagnoff. (2004). IkappaB-kinasebeta-dependent NF-kappaB activation provides radioprotection to the intestinal epithelium. Proc Natl Acad Sci U S A, 101(8), 2452-2457. DOI : 10.1073/pnas.0306734101
- Abdollahi, H. (2014). Probiotic-based protection of normal tissues during radiotherapy. Nutrition, 30(4), 495-496. DOI : 10.1016/j.nut.2013.09.006
- Abdollahi, H. (2015). Beneficial effects of cellular autofluorescence following ionization radiation: Hypothetical approaches for radiation protection and enhancing radiotherapy effectiveness. Med Hypotheses., 84(3), 194-198. DOI : 10.1016/j.mehy.2014.12.021
- Son, J. C. (2013). Phospholipase D inhibitor enhances radiosensitivity of breast cancer cells. Exp Mol Med, 45(8), e38. DOI : 10.1038/emm.2013.75
- W. Kim, K. Seong, B. Youn. (2011). Phenylpropanoids in radioregulation: double edged sword. Exp Mol Med, 43(6), 323-333. DOI : 10.3858/emm.2011.43.6.034
- Wedlake, L. J. et al. (2012). Evaluating the efficacy of statins and ACE-inhibitors in reducing gastrointestinal toxicity in patients receiving radiotherapy for pelvic malignancies. Br J Pharmacol, 164(8), 2064- 2072. DOI : 10.1016/j.ejca.2011.12.034
- Murley, J. S., Nantajit, D., Baker, K. L., Kataoka, Y., Li, J. J., & Grdina, D. J. (2008). Maintenance of manganese superoxide dismutase (SOD2)-mediated delayed radioprotection induced by repeated administration of the free thiol form of amifostine. Radiat Res, 169(5), 495-505. DOI : 10.1667/RR1194.1
- Xie, J. et al. (2017). Therapeutic Nanoparticles Based on Curcumin and Bamboo Charcoal Nanoparticles for Chemo-Photothermal Synergistic Treatment of Cancer and Radioprotection of Normal Cells. ACS Appl Mater Interfaces, 9(16), 14281-14291 DOI : 10.1021/acsami.7b02622
- Bjorklund, G., Semenova, Y., Pivina, L., Dadar, M., Rahman, M. M., Aaseth, J., & Chirumbolo, S. (2020). Uranium in drinking water: a public health threat. Arch Toxicol, 94(5), 1551-1560. DOI : 10.1007/s00204-020-02676-8
- V P Wellner, M E Anderson, R N Puri, G L Jensen, A Meister (2012). Radioprotection by glutathione ester: transport of glutathione ester into human lymphoid cells and fibroblasts. Proc Natl Acad Sci U S A, 81(15), 4732-4735. DOI: 10.1073/pnas.81.15.4732
- Yu, H., Aravindan, N., Xu, J., & Natarajan, M. (2017). Inter- and intra-cellular mechanism of NF-kB-dependent survival advantage and clonal expansion of radio-resistant cancer cells. Cell Signal, 31, 105-111. DOI : 10.1016/j.cellsig.2017.01.011
- Sitko, J. C. et al. (2008). SOCS3 regulates p21 expression and cell cycle arrest in response to DNA damage. Cellular signalling, 20(12), 2221-2230. DOI : 10.1016/j.cellsig.2008.08.011
- Nalla, A. K., Gogineni, V. R., Gupta, R., Dinh, D. H., & Rao, J. S. (2011). Suppression of uPA and uPAR blocks radiation-induced MCP-1 mediated recruitment of endothelial cells in meningioma. Cell Signal, 23(8), 1299-1230 DOI : 10.1016/j.cellsig.2011.03.011
- Floyd, R. A. (1990). The role of 8-hydroxyguanine in carcinogenesis. Carcinogenesis, 11(9), 1447-1450 DOI : 10.1093/carcin/11.9.1447
- T. Kim, T. Huang, J. Jang, M. Kim, H. Kim, J. Lee, J. Pack, J. Seo, W. Park. (2008). Local exposure of 849 MHz and 1763 MHz radiofrequency radiation to mouse heads does not induce cell death or cell proliferation in brain. Exp Mol Med, 40(3), 294-303. DOI: 10.3858/emm.2008.40.3.294
- Gerschman, R., Gilbert, D. L., Nye, S. W., Dwyer, P., & Fenn, W. O. (1954). Oxygen poisoning and x-irradiation: a mechanism in common. Science, 119(3097), 623-626. DOI: 10.1126/science.119.3097.623
- Xu, W., Yang, F., Shen, X., Fan, S., Liu, Q., & Wang, D. (2014). Polysaccharide isolated from Parmelia tinctorum ameliorates ionizing irradiation-induced damage in mice. J Radiat Res, 55(4), 641-647. DOI : 10.1093/jrr/rrt224
- Csondor, K., Bajak, P., Surbeck, H., Izsak, B., Horvath, A., Vargha, M., & Eross, A. (2020). Transient nature of riverbank filtered drinking water supply systems - A new challenge of natural radioactivity assessment. J Environ Radioact, 211, 106072. DOI : 10.1016/j.jenvrad.2019.106072
- Pal, R., Patra, A. C., Bakshi, A. K., Dhabekar, B., Reddy, P. J., Sengupta, P., & Sapra, B. K. (2021). Investigations on baseline levels for natural radioactivity in soils, rocks, and lakes of Larsemann Hills in East Antarctica. Environ Monit Assess, 193(12), 822. DOI : 10.1007/s10661-021-09446-8