Ansari Mojtaba, Rezaei-Tavirani Mostafa, Hamzeloo-Moghadam Maryam, Razzaghi Mohhamadreza, Arjmand Babak, Zamanian Azodi Mona, Khodadoost Mahmood, Okhovatian Farshad
Faculty of Medicine, Imam Hosein Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Proteomics Research Center, Faculty of Paramedical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
J Lasers Med Sci. 2022 Aug 27;13:e35. doi: 10.34172/jlms.2022.35. eCollection 2022.
Understanding the molecular mechanism of chronic low-dose ionizing radiation (LDIR) effects on the human body is the subject of many research studies. Several aspects of cell function such as cell proliferation, apoptosis, inflammation, and tumorigenesis are affected by LDIR. Detection of the main biological process that is targeted by LIDR via network analysis is the main aim of this study. GSE66720 consisting of gene expression profiles of human umbilical vein endothelial cells (HUVECs) (a suitable cell line to be investigated), including irradiated and control cells, was downloaded from Gene Expression Omnibus (GEO). The significant differentially expressed genes (DEGs) were determined and analyzed via protein-protein interaction (PPI) network analysis to find the central individuals. The main cell function which was related to the central nodes was introduced. Among 64 queried DEGs, 48 genes were recognized by the STRING database. C-X-C motif chemokine ligand 8 (CXCL8), intercellular adhesion molecule 1 (ICAM1), Melanoma growth-stimulatory activity/growth-regulated protein α (CXCL1), vascular cell adhesion molecule 1 (VCAM-1), and nerve growth factor (NGF) were introduced as hub nodes. Findings indicate that inflammation is the main initial target of LDIR at the cellular level which is associated with alteration in the other essential functions of the irradiated cells.
了解慢性低剂量电离辐射(LDIR)对人体影响的分子机制是许多研究的主题。细胞功能的几个方面,如细胞增殖、凋亡、炎症和肿瘤发生,都受到LDIR的影响。通过网络分析检测LDIR所靶向的主要生物学过程是本研究的主要目的。从基因表达综合数据库(GEO)下载了GSE66720,它由人脐静脉内皮细胞(HUVECs,一种适合研究的细胞系)的基因表达谱组成,包括辐照细胞和对照细胞。通过蛋白质-蛋白质相互作用(PPI)网络分析确定并分析显著差异表达基因(DEGs),以找到核心个体。介绍了与核心节点相关的主要细胞功能。在64个查询的DEGs中,STRING数据库识别出48个基因。C-X-C基序趋化因子配体8(CXCL8)、细胞间黏附分子1(ICAM1)、黑色素瘤生长刺激活性/生长调节蛋白α(CXCL1)、血管细胞黏附分子1(VCAM-1)和神经生长因子(NGF)被引入作为枢纽节点。研究结果表明,炎症是LDIR在细胞水平上的主要初始靶点,这与辐照细胞其他基本功能的改变有关。