Department of General Biology and Genomics, Institute of Cell Biology and Biotechnology, L.N. Gumilyov Eurasian National University, Astana 010008, Kazakhstan.
Int J Mol Sci. 2024 Aug 2;25(15):8446. doi: 10.3390/ijms25158446.
Exposure to ionizing radiation can result in the development of a number of diseases, including cancer, cataracts and neurodegenerative pathologies. Certain occupational groups are exposed to both natural and artificial sources of radiation as a consequence of their professional activities. The development of non-invasive biomarkers to assess the risk of exposure to ionizing radiation for these groups is of great importance. In this context, our objective was to identify epigenetic and molecular biomarkers that could be used to monitor exposure to ionizing radiation. The impact of X-ray exposure on the miRNAs profile and the level of cf mtDNA were evaluated using the RT-PCR method. The levels of pro-inflammatory cytokines in their blood were quantified using the ELISA method. A significant decrease in miR-19a-3p, miR-125b-5p and significant increase in miR-29a-3p was observed in the blood plasma of individuals exposed to X-ray. High levels of pro-inflammatory cytokines and cf mtDNA were also detected. In silico identification of potential targets of these miRNAs was conducted using MIENTURNET. VDAC1 and ALOX5 were identified as possible targets. Our study identified promising biomarkers such as miRNAs and cf mtDNA that showed a dose-dependent effect of X-ray exposure.
接触电离辐射会导致多种疾病的发生,包括癌症、白内障和神经退行性病变。某些职业群体由于其职业活动而接触到天然和人工辐射源。开发非侵入性生物标志物来评估这些群体接触电离辐射的风险非常重要。在这种情况下,我们的目标是确定可以用于监测电离辐射暴露的表观遗传和分子生物标志物。使用 RT-PCR 方法评估了 X 射线暴露对 miRNA 谱和 cf mtDNA 水平的影响。使用 ELISA 方法定量了其血液中的促炎细胞因子水平。在暴露于 X 射线的个体的血浆中观察到 miR-19a-3p、miR-125b-5p 的显著降低和 miR-29a-3p 的显著增加。还检测到高水平的促炎细胞因子和 cf mtDNA。使用 MIENTURNET 对这些 miRNA 的潜在靶标进行了计算机识别。VDAC1 和 ALOX5 被鉴定为可能的靶标。我们的研究确定了有前途的生物标志物,如 miRNA 和 cf mtDNA,它们显示出 X 射线暴露的剂量依赖性效应。