Effects of oxygen on the response of mitochondria to X-irradiation and reactive oxygen species-mediated fibroblast activation

References

• Anoopkumar-Dukie S, Conere T, Sisk GD, Allshire A. 2009. Mitochondrial modulation of oxygen-dependent radiosensitivity in some human tumour cell lines. Br J Radiol. 82(982):847–854.
   PubMed Web of Science ®Google Scholar
• Azzam EI, Jay-Gerin JP, Pain D. 2012. Ionizing radiation-induced metabolic oxidative stress and prolonged cell injury. Cancer Lett. 327(1–2):48–60.
   PubMed Web of Science ®Google Scholar
• Berzaghi R, Islam A, Hellevik T, Martinez-Zubiaurre I. 2021a. Secretion rates and protein composition of extracellular vesicles released by cancer-associated fibroblasts after radiation. J Radiat Res. 62(3):401–413.
   PubMed Web of Science ®Google Scholar
• Berzaghi R, Tornaas S, Lode K, Hellevik T, Martinez-Zubiaurre I. 2021b. Ionizing radiation curtails immunosuppressive effects from cancer-associated fibroblasts on dendritic cells. Front Immunol. 12:662594.
   PubMed Web of Science ®Google Scholar
• Boice JD, Quinn B, Al-Nabulsi I, Ansari A, Blake PK, Blattnig SR, Caffrey EA, Cohen SS, Golden AP, Held KD, et al. 2022. A million persons, a million dreams: a vision for a national center of radiation epidemiology and biology. Int J Radiat Biol. 98(4):795–821.
   PubMed Web of Science ®Google Scholar
• Brown GC. 1992. Control of respiration and ATP synthesis in mammalian mitochondria and cells. Biochem J. 284(1):1–13.
   PubMedGoogle Scholar
• Desagher S, Martinou JC. 2000. Mitochondria as the central control point of apoptosis. Trends Cell Biol. 10(9):369–377.
   PubMed Web of Science ®Google Scholar
• Diegelmann RF, Evans MC. 2004. Wound healing: an overview of acute, fibrotic and delayed healing. Front Biosci. 9:283–289.
   PubMed Web of Science ®Google Scholar
• Domogauer JD, de Toledo SM, Howell RW, Azzam EI. 2021. Acquired radioresistance in cancer associated fibroblasts is concomitant with enhanced antioxidant potential and DNA repair capacity. Cell Commun Signal. 19(1):30.
   PubMed Web of Science ®Google Scholar
• Ewing D. 1998. The oxygen fixation hypothesis: a reevaluation. Am J Clin Oncol. 21(4):355–361.
   PubMed Web of Science ®Google Scholar
• Floyd RA. 1990. The role of 8-hydroxyguanine in carcinogenesis. Carcinogenesis. 11(9):1447–1450.
   PubMed Web of Science ®Google Scholar
• Hartupee J, Mann DL. 2016. Role of inflammatory cells in fibroblast activation. J Mol Cell Cardiol. 93:143–148.
   PubMed Web of Science ®Google Scholar
• Hellevik T, Pettersen I, Berg V, Winberg JO, Moe BT, Bartnes K, Paulssen RH, Busund L-T, Bremnes R, Chalmers A, et al. 2012. Cancer-associated fibroblasts from human NSCLC survive ablative doses of radiation but their invasive capacity is reduced. Radiat Oncol. 7:59.
   PubMed Web of Science ®Google Scholar
• Hernansanz-Agustín P, Enríquez JA. 2021. Generation of reactive oxygen species by mitochondria. Antioxidants. 10(3):415.
   Web of Science ®Google Scholar
• Howard-Flanders P, Alper T. 1957. The sensitivity of microorganisms to irradiation under controlled gas conditions. Radiat Res. 7(5):518–540.
   PubMed Web of Science ®Google Scholar
• Iorio R, Celenza G, Petricca S. 2021. Mitophagy: molecular mechanisms, new concepts on Parkin activation and the emerging role of AMPK/ULK1 axis. Cells. 11(1):30.
   PubMed Web of Science ®Google Scholar
• Kalyanaraman B, Darley-Usmar V, Davies KJA, Dennery PA, Forman HJ, Grisham MB, Mann GE, Moore K, Roberts LJ, Ischiropoulos H, et al. 2012. Measuring reactive oxygen and nitrogen species with fluorescent probes: challenges and limitations. Free Radic Biol Med. 52(1):1–6.
   PubMed Web of Science ®Google Scholar
• Kam WW, Banati RB. 2013. Effects of ionizing radiation on mitochondria. Free Radic Biol Med. 65:607–619.
   PubMed Web of Science ®Google Scholar
• Kasai S, Shimizu S, Tatara Y, Mimura J, Itoh K. 2020. Regulation of Nrf2 by mitochondrial reactive oxygen species in physiology and pathology. Biomolecules. 10(2):320.
   PubMed Web of Science ®Google Scholar
• Leach JK, Van Tuyle G, Lin PS, Schmidt-Ullrich R, Mikkelsen RB. 2001. Ionizing radiation-induced, mitochondria-dependent generation of reactive oxygen/nitrogen. Cancer Res. 61(10):3894–3901.
   PubMed Web of Science ®Google Scholar
• Littbrand B, Révész L. 1969. The effect of oxygen on cellular survival and recovery after radiation. Br J Radiol. 42(504):914–924.
   PubMed Web of Science ®Google Scholar
• Liu R, Bian Y, Liu L, Liu L, Liu X, Ma S. 2022. Molecular pathways associated with oxidative stress and their potential applications in radiotherapy. Int J Mol Med. 49(5):5121.
   Web of Science ®Google Scholar
• Maeda M, Oe M. 2017. Mental health consequences and social issues after the Fukushima disaster. Asia Pac J Public Health. 29(2_suppl):36S–46S.
   PubMedGoogle Scholar
• Matsuoka Y, Yoshida R, Kawahara K, Sakata J, Arita H, Nkashima H, Takahashi N, Hirayama M, Nagata M, Hirosue A, et al. 2022. The antioxidative stress regulator Nrf2 potentiates radioresistance of oral squamous cell carcinoma accompanied with metabolic modulation. Lab Invest. 102(8):896–907.
   PubMed Web of Science ®Google Scholar
• Maynard S, Schurman SH, Harboe C, de Souza-Pinto NC, Bohr VA. 2009. Base excision repair of oxidative DNA damage and association with cancer and aging. Carcinogenesis. 30(1):2–10.
   PubMed Web of Science ®Google Scholar
• Michaels HB, Hunt JW. 1977. Reaction of oxygen with radiation-induced free radicals on single-stranded polynucleotides. Radiat Res. 72(1):18–31.
   PubMed Web of Science ®Google Scholar
• Mortezaee K, Majidpoor J. 2022. Roles for macrophage-polarizing interleukins in cancer immunity and immunotherapy. Cell Oncol. 45(3):333–353.
   Web of Science ®Google Scholar
• Nuclear-and-Radiation-Studies-Board. 2019. The future of low dose radiation research in the United States: proceedings of a symposium. O. Kosti, editor. Washington DC: 2019 by the National Academy of Sciences.
   Google Scholar
• Repussard J. 2018. Outcome of the European initiative for radiation protection research and future perspectives. Ann ICRP. 47(3–4):91–96.
   PubMedGoogle Scholar
• Richardson RB, Harper ME. 2016. Mitochondrial stress controls the radiosensitivity of the oxygen effect: implications for radiotherapy. Oncotarget. 7(16):21469–21483.
   PubMedGoogle Scholar
• Robinson KM, Janes MS, Pehar M, Monette JS, Ross MF, Hagen TM, Murphy MP, Beckman JS. 2006. Selective fluorescent imaging of superoxide in vivo using ethidium-based probes. Proc Natl Acad Sci USA. 103(41):15038–15043.
   PubMed Web of Science ®Google Scholar
• Salomaa S, Jourdain J-R, Kreuzer M, Jung T, Repussard J. 2017. Multidisciplinary European low dose initiative: an update of the MELODI program. Int J Radiat Biol. 93(10):1035–1039.
   PubMed Web of Science ®Google Scholar
• Shimura T, Ando T, Narao M, Sasatani M, Kamiya K, Ushiyama A. 2020. Mechanism of turnover or persistence of radiation-induced myofibroblast in vitro. Cell Cycle. 19(23):3375–3385.
   PubMed Web of Science ®Google Scholar
• Shimura T, Kakuda S, Ochiai Y, Nakagawa H, Kuwahara Y, Takai Y, Kobayashi J, Komatsu K, Fukumoto M. 2010. Acquired radioresistance of human tumor cells by DNA-PK/AKT/GSK3 beta-mediated cyclin D1 overexpression. Oncogene. 29(34):4826–4837.
   PubMed Web of Science ®Google Scholar
• Shimura T, Sasatani M, Kamiya K, Kawai H, Inaba Y, Kunugita N. 2016. Mitochondrial reactive oxygen species perturb AKT/cyclin D1 cell cycle signaling via oxidative inactivation of PP2A in lowdose irradiated human fibroblasts. Oncotarget. 7(3):3559–3570.
   PubMed Web of Science ®Google Scholar
• Shimura T, Sasatani M, Kawai H, Kamiya K, Kobayashi J, Komatsu K, Kunugita N. 2018. Radiation-induced myofibroblasts promote tumor growth via mitochondrial ROS-activated TGFβ signaling. Mol Cancer Res. 16(11):1676–1686.
   PubMed Web of Science ®Google Scholar
• Shimura T, Toyoshima M, Adiga SK, Kunoh T, Nagai H, Shimizu N, Inoue M, Niwa O. 2006. Suppression of replication fork progression in low-dose-specic p53-dependent S-phase DNA damage checkpoint. Oncogene. 25(44):5921–5932.
   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(3–4):311–322.
   PubMed Web of Science ®Google Scholar
• Stuart JA, Fonseca J, Moradi F, Cunningham C, Seliman B, Worsfold CR, Dolan S, Abando J, Maddalena LA. 2018. How supraphysiological oxygen levels in standard cell culture affect oxygen-consuming reactions. Oxid Med Cell Longev. 2018:8238459.
   PubMed Web of Science ®Google Scholar
• Sugimori F, Hirakawa H, Tsutsui A, Yamaji H, Komaru S, Takasaki M, Iwamatsu T, Uemura T, Uemura Y, Morita K, et al. 2019. A novel electron emission-based cell culture device promotes cell proliferation and differentiation of pre-osteoblastic MC3T3-E1 cells. PLoS One. 14(3):e0213579.
   PubMed Web of Science ®Google Scholar
• UNSCEAR 2018 Sources. 2018. Effects and risks of ionizing radiation, United Nations Scientific Committee on the Effects of Atomic Radiation (UNSCEAR) 2017 Report: United Nations.
   Google Scholar
• Wang Y, Nartiss Y, Steipe B, McQuibban GA, Kim PK. 2012. ROS-induced mitochondrial depolarization initiates PARK2/PARKIN-dependent mitochondrial degradation by autophagy. Autophagy. 8(10):1462–1476.
   PubMed Web of Science ®Google Scholar
• Yang N, Lode K, Berzaghi R, Islam A, Martinez-Zubiaurre I, Hellevik T. 2020. Irradiated tumor fibroblasts avoid immune recognition and retain immunosuppressive functions over natural killer cells. Front Immunol. 11:602530.
   PubMed Web of Science ®Google Scholar
• Yoshida T, Goto S, Kawakatsu M, Urata Y, Li T-S. 2012. Mitochondrial dysfunction, a probable cause of persistent oxidative stress after exposure to ionizing radiation. Free Radic Res. 46(2):147–153.
   PubMed Web of Science ®Google Scholar