The Role of Natural Background Radiation in Maintaining Genomic Stability in the CGL1 Human Hybrid Model System

电离辐射 DNA损伤 癌变 生物 放射生物学 克隆形成试验 碱性磷酸酶 本底辐射 DNA修复 毒理 辐照 细胞 癌症研究 男科 基因 遗传学 辐射 DNA 放射治疗 医学 生物化学 内科学 物理 光学 核物理学
作者
Jake Pirkkanen,Taylor Laframboise,Jayden Peterson,Alyssa Labelle,Forest Mahoney,Michel Lapointe,Marc S. Mendonca,T.C. Tai,Simon J. Lees,Sujeenthar Tharmalingam,Douglas R. Boreham,Christopher Thome
出处
期刊:Radiation Research [BioOne (Radiation Research Society)]
标识
DOI:10.1667/rade-23-00243.1
摘要

Natural background ionizing radiation is present on the earth’s surface; however, the biological role of this chronic low-dose-rate exposure remains unknown. The Researching the Effects of the Presence and Absence of Ionizing Radiation (REPAIR) project is examining the impacts of sub-natural background radiation exposure through experiments conducted 2 km underground in SNOLAB. The rock overburden combined with experiment-specific shielding provides a background radiation dose rate 30 times lower than on the surface. We hypothesize that natural background radiation is essential for life and maintains genomic stability and that prolonged exposure to sub-background environments will be detrimental to biological systems. To evaluate this, human hybrid CGL1 cells were continuously cultured in SNOLAB and our surface control laboratory for 16 weeks. Cells were assayed every 4 weeks for growth rate, alkaline phosphatase (ALP) activity (a marker of cellular transformation in the CGL1 system), and the expression of genes related to DNA damage and cell cycle regulation. A subset of cells was also exposed to a challenge radiation dose (0.1 to 8 Gy of X rays) and assayed for clonogenic survival and DNA double-strand break induction to examine if prolonged sub-background exposure alters the cellular response to high-dose irradiation. At each 4-week time point, sub-background radiation exposure did not significantly alter cell growth rates, survival, DNA damage, or gene expression. However, cells cultured in SNOLAB showed significantly higher ALP activity, a marker of carcinogenesis in these cells, which increased with longer exposure to the sub-background environment, indicative of neoplastic progression. Overall, these data suggest that sub-background radiation exposure does not impact growth, survival, or DNA damage in CGL1 cells but may lead to increased rates of neoplastic transformation, highlighting a potentially important role for natural background radiation in maintaining normal cellular function and genomic stability.

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