1. 1. Rithidech KN, Golightly M, Whorton E (2008) Analysis of cell cycle in mouse bone marrow cells following acute in vivo exposure to 56Fe ions. J Radiat Res, 49(4):437-43. [ DOI:10.1269/jrr.07109] 2. Jelveh S, Kaspler P, Bhogal N, Mahmood J, Lindsay PE, Okunieff P, et al. (2013) Investigations of antioxidant-mediated protection and mitigation of radiation-induced DNA damage and lipid peroxidation in murine skin. Int J Radiat Biol, 89(8): 618-27. [ DOI:10.3109/09553002.2013.782450] 3. Villani P, Fresegna AM, Ranaldi R, Eleuteri P, Paris L, Pacchierotti F, et al. (2013) X-ray induced DNA damage and repair in germ cells of PARP1(-/-) male mice. Int J Mol Sci,14(9):18078-92. [ DOI:10.3390/ijms140918078] 4. Mozdarani H, Salimi M, Bakhtari N (2017) Inherent radiosensitivity and its impact on breast cancer chemo-radiotherapy. Int J Radiat Res,15(4):325-41. 5. Bond VP, Benary V, Sondhaus CA (1991) A different perception of the linear, nonthreshold hypothesis for low-dose irradiation. Proc Natl Acad Sci USA, 88(19):8666-70. [ DOI:10.1073/pnas.88.19.8666] 6. Azzam EI, de Toledo SM, Raaphorst GP, Mitchel RE (1996) Low-dose ionizing radiation decreases the frequency of neoplastic transformation to a level below the spontaneous rate in C3H 10T1/2 cells. Radiat Res,146(4):369-73. [ DOI:10.2307/3579298] 7. Wolff S (1998) The adaptive response in radiobiology: evolving insights and implications. Environ Health Perspect, 106 Suppl 1: 277-83. [ DOI:10.1289/ehp.98106s1277] 8. Redpath JL, Liang D, Taylor TH, Christie C, Elmore E (2001) The shape of the dose-response curve for radiation-induced neoplastic transformation in vitro: evidence for an adaptive response against neoplastic transformation at low doses of low-LET radiation. Radiat Res,156(6): 700-7. [ DOI:10.1667/0033-7587(2001)156[0700:TSOTDR]2.0.CO;2] 9. Feinendegen LE (2005) Evidence for beneficial low level radiation effects and radiation hormesis. Br J Radiol, 78(925): 3-7. [ DOI:10.1259/bjr/63353075] 10. Scott BR and Di Palma J (2006) Sparsely ionizing diagnostic and natural background radiations are likely preventing cancer and other genomic-instability-associated diseases. Dose Response, 5(3): 230-55. [ DOI:10.2203/dose-response.06-002.Scott] 11. Rithidech KN and Scott BR (2008) Evidence for radiation hormesis after in vitro exposure of human lymphocytes to low doses of ionizing radiation. Dose Response,6(3): 252-71. [ DOI:10.2203/dose-response.07-024.Rithidech] 12. Hamada N, Matsumoto H, Hara T, Kobayashi Y (2007) Intercellular and intracellular signaling pathways mediating ionizing radiation-induced bystander effects. J Radiat Res, 48(2): 87-95. [ DOI:10.1269/jrr.06084] 13. Huang YH, Yang PM, Chuah QY, Lee YJ, Hsieh YF, Peng CW, et al. (2014) Autophagy promotes radiation-induced senescence but inhibits bystander effects in human breast cancer cells. Autophagy,10(7): 1212-28. [ DOI:10.4161/auto.28772] 14. Chen ZY, Hu YY, Hu XF, Cheng LX (2018) The conditioned medium of human mesenchymal stromal cells reduces irradiation-induced damage in cardiac fibroblast cells. J Radiat Res, 59(5): 555-64. [ DOI:10.1093/jrr/rry048] 15. Azzam EI, de Toledo SM, Little JB (2003) Oxidative metabolism, gap junctions and the ionizing radiation-induced bystander effect. Oncogene, 22(45): 7050-7. [ DOI:10.1038/sj.onc.1206961] 16. Mahmoudi F, Shahbazi-Gahrouei D, Chegeni N, Saeb M, Sadeghi V, Hemati S (2022) Potential implications of the radiation-induced bystander effect for spatially fractionated radiotherapy: A theoretical simulation study. Int J Radiat Res, 20(3): 657-64. 17. Ramadan LM and Abdelrazzak AB (2024) The non-targeted effect increases the risk of the radiation-induced myocardial injury. Int J Radiat Res, 22(2): 289-95. [ DOI:10.61186/ijrr.22.2.289] 18. Rezaei M, Kamran Samani R, Kazemi M, Shanei A, Hejazi SH (2021) Induction of a bystander effect after therapeutic ultrasound exposure in human melanoma: In-vitro assay. Int J Radiat Res,19(1): 183-9. [ DOI:10.29252/ijrr.19.1.183] 19. Shirani S, Mozdarani H, Mahmoodzadeh A, Salimi M (2015) Radio-adaptive response of peripheral blood lymphocytes following bystander effects induced by preirradiated CHO-K1 cells using the micronucleus assay. Int J Radiat Res,13(2):151-6. 20. Bahreyni Toossi MT, Khademi S, Azimian H, Mohebbi S, Soleymanifard S (2017) Assessment of the dose-response relationship of radiation-induced bystander effect in two cell lines exposed to high doses of ionizing radiation (6 and 8 Gy). Cell J, 19(3): 434-42. 21. Faqihi F, Neshastehriz A, Soleymanifard S, Shabani R, Eivazzadeh N (2015) Radiation-induced bystander effect in non-irradiated glioblastoma spheroid cells. J Radiat Res, 56(5): 777-83. [ DOI:10.1093/jrr/rrv039] 22. Tungjai M, Phathakanon N, Rithidech KN (2017) Effects of medical diagnostic low-dose X rays on human lymphocytes: Mitochondrial membrane potential, apoptosis and cell cycle. Health Phys, 112(5): 458-64. [ DOI:10.1097/HP.0000000000000647] 23. Tungjai M, Phathakanon N, Ketnuam P, Tinlapat J, Kothan S (2018) Determination of hemolysis, osmotic fragility and fluorescence anisotropy on irradiated red blood cells as a function of kV of medical diagnostic X-rays. Int J Radiat Res,16(1): 123-7. 24. Tungjai M, Sopapang J, Tasri N, Osothsongkroh C, Jantarato A, Kothan S (2019) The effects of medical diagnostic low dose X-rays after in-vitro exposure of human red blood cells: Hemolysis and osmotic fragility. ToxEHS, 11(3): 237-43. [ DOI:10.1007/s13530-019-0409-1] 25. Supawat B, Homnuan P, Kanthawong N, Semrasa N, Tima S, Kothan S, et al. (2021) Different responses of normal cells (red blood cells) and cancer cells (K562 and K562/Dox cells) to low-dose 137Cs gamma‑rays. Mol Clin Oncol, 14(4): 74. [ DOI:10.3892/mco.2021.2236] 26. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. (2021) Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin, 71(3): 209-49. [ DOI:10.3322/caac.21660] 27. Zhong S, Chen Z, Yu X, Chen W, Lv M, Ma T, et al. (2014) Tea consumption and leukemia risk: a meta-analysis. Tumour Biol, 35(6): 5205-12. [ DOI:10.1007/s13277-014-1675-9] 28. Mahbub AA, Le Maitre CL, Haywood-Small SL, McDougall GJ, Cross NA, Jordan-Mahy N (2013) Differential effects of polyphenols on proliferation and apoptosis in human myeloid and lymphoid leukemia cell lines. Anticancer Agents Med Chem,13(10): 1601-13. [ DOI:10.2174/18715206113139990303] 29. Liu X, Ye F, Wu J, How B, Li W, Zhang DY (2015) Signaling proteins and pathways affected by flavonoids in leukemia cells. Nutr Cancer,67(2): 238-49. [ DOI:10.1080/01635581.2015.989372] 30. Davenport A, Frezza M, Shen M, Ge Y, Huo C, Chan TH, et al. (2010) Celastrol and an EGCG pro-drug exhibit potent chemosensitizing activity in human leukemia cells. Int J Mol Med, 25(3): 465-70. [ DOI:10.3892/ijmm_00000366] 31. Gewirtz DA (1999) A critical evaluation of the mechanisms of action proposed for the antitumor effects of the anthracycline antibiotics adriamycin and daunorubicin. Biochem Pharmacol, 57(7): 727-41. [ DOI:10.1016/S0006-2952(98)00307-4] 32. Minotti G, Menna P, Salvatorelli E, Cairo G, Gianni L (2004) Anthracyclines: molecular advances and pharmacologic developments in antitumor activity and cardiotoxicity. Pharmacol Rev, 56(2):185-229. [ DOI:10.1124/pr.56.2.6] 33. Meredith AM and Dass CR (2016) Increasing role of the cancer chemotherapeutic doxorubicin in cellular metabolism. J Pharm Pharmacol, 68(6):729-41. [ DOI:10.1111/jphp.12539] 34. Supawat B, Moungthong P, Chanloi C, Jindachai N, Tima S, Kothan S, et al. (2020) Effects of gadolinium-based magnetic resonance imaging contrast media on red blood cells and K562 cancer cells. J Trace Elem Med Biol, 62:126640. [ DOI:10.1016/j.jtemb.2020.126640] 35. Arbab IA, Abdul AB, Sukari MA, Abdullah R, Syam S, Kamalidehghan B, et al. (2013) Dentatin isolated from Clausena excavata induces apoptosis in MCF-7 cells through the intrinsic pathway with involvement of NF-κB signalling and G0/G1 cell cycle arrest: a bioassay-guided approach. J Ethnopharmacol, 145(1): 343-54. [ DOI:10.1016/j.jep.2012.11.020] 36. Kntayya SB, Ibrahim MD, Mohd Ain N, Iori R, Ioannides C, Abdull Razis AF (2018) Induction of apoptosis and cytotoxicity by isothiocyanate sulforaphene in human hepatocarcinoma HepG2 cells. Nutrients, 10(6). [ DOI:10.3390/nu10060718] 37. Aye KT, Wattanapongpitak S, Supawat B, Kothan S, Udomtanakunchai C, Tima S, et al. (2021) Gallic acid enhances pirarubicin‑induced anticancer in living K562 and K562/Dox leukemia cancer cells through cellular energetic state impairment and P-glycoprotein inhibition. Oncol Rep, 46(4): 1-10. [ DOI:10.3892/or.2021.8178] 38. Supawat B, Udomtanakunchai C, Kothan S, Tungjai M (2019) The effects of iodinated radiographic contrast media on multidrug-resistant K562/Dox cells: Mitochondria impairment and P-glycoprotein inhibition. Cell Biochem Biophys, 77(2): 157-63. [ DOI:10.1007/s12013-019-00868-3] 39. Loetchutinat C, Kothan S, Dechsupa S, Meesungnoen J, Jay-Gerin J-P, Mankhetkorn S (2005) Spectrofluorometric determination of intracellular levels of reactive oxygen species in drug-sensitive and drug-resistant cancer cells using the 2′,7′-dichlorofluorescein diacetate assay. Radiat Phys Chem,72: 323-31. [ DOI:10.1016/j.radphyschem.2004.06.011] 40. Herok R, Konopacka M, Polanska J, Swierniak A, Rogolinski J, Jaksik R, et al. (2010) Bystander effects induced by medium from irradiated cells: similar transcriptome responses in irradiated and bystander K562 cells. Int J Radiat Oncol Biol Phys, 77(1): 244-52. [ DOI:10.1016/j.ijrobp.2009.11.033] 41. Ayala A, Muñoz MF, Argüelles S (2014) Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal. Oxid Med Cell Longev, 2014: 360438. [ DOI:10.1155/2014/360438] 42. Yin H, Xu L, Porter NA (2011) Free radical lipid peroxidation: mechanisms and analysis. Chem Rev, 111(10): 5944-72. [ DOI:10.1021/cr200084z] 43. Sokolov MV and Neumann RD (2010) Radiation-induced bystander effects in cultured human stem cells. PLoS One, 5(12): e14195. [ DOI:10.1371/journal.pone.0014195] 44. Soleymanifard S, Bahreyni Toossi MT, Sazgarnia A, Mohebbi S (2013) The role of target and bystander cells in dose-response relationship of radiation-induced bystander effects in two cell lines. Iran J Basic Med Sci, 16(2): 177-83. 45. Soleymanifard S, Toossi MT, Samani RK, Mohebbi S (2014) Investigation of the bystander effect in MRC5 cells after acute and fractionated irradiation in vitro. J Med Phys, 39(2): 93-7. [ DOI:10.4103/0971-6203.131282] 46. Jabbari N, Nawaz M, Rezaie J (2019) Bystander effects of ionizing radiation: conditioned media from X-ray irradiated MCF-7 cells increases the angiogenic ability of endothelial cells. Cell Commun Signal, 17(1): 165. [ DOI:10.1186/s12964-019-0474-8]
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