健康吸烟者人小气道上皮差异表达基因分析显示氧化应激和炎症引起疾病的潜在风险以及虾青素作为抗炎剂的潜力

IF 2.6 Q3 IMMUNOLOGY International Journal of Inflammation Pub Date : 2023-01-01 DOI:10.1155/2023/4251299
Irandi Putra Pratomo, Aryo Tedjo, Dimas R Noor, Rosmalena
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摘要

香烟烟雾(CS)因其增加氧化应激的作用而闻名,氧化应激可引发自由基和活性氧(ROS)介导的组织损伤和内皮功能障碍。ROS本身是一种关键的信号分子,在炎症性疾病的发展中发挥作用。核因子红细胞2相关因子2 (Nrf2)是抗氧化细胞对CS引起的细胞和组织破坏成分反应的主要调节因子。Nrf2蛋白在吸烟者的小气道上皮中显著激活,随后在相同的细胞中发生一系列基因表达变化。本研究旨在观察吸烟者人小气道上皮中差异表达基因(DEGs)与因虾青素(AST)处理而表达变化的基因(AST是一种可以调节Nrf2的抗氧化化合物)的比较。使用GEO2R分析存储在GEO浏览器(GSE 11952)中的基因表达数据,在吸烟者和非吸烟者中搜索DEG。DEG进一步与那些由于虾青素处理(AST)而表达改变的基因进行比较,这些基因来自比较毒物基因组数据库(CTD;https://ctdbase.org/)。DEG (p < 0.05)分析结果显示,与AST治疗相比,有23个基因的表达调控发生逆转。23个DEGs的基因功能注释显示,其中一些基因参与化学和氧化应激、活性氧(ROS)和凋亡信号通路。所有的基因都与慢性支气管炎、肺腺癌、非小细胞肺癌、肺癌、小细胞肺癌、2型糖尿病、肺气肿、缺血性中风、肺部疾病和炎症有关。因此,对吸烟者进行AST治疗可能会潜在地减少ROS和氧化应激的发展,从而导致与吸烟相关的炎症和健康风险。
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Differentially Expressed Genes Analysis in the Human Small Airway Epithelium of Healthy Smokers Shows Potential Risks of Disease Caused by Oxidative Stress and Inflammation and the Potentiality of Astaxanthin as an Anti-Inflammatory Agent.

Cigarette smoke (CS) was known for its effect of increasing oxidative stress that could trigger tissue injury and endothelial dysfunction mediated by free radicals and reactive oxygen species (ROS). ROS itself is a key signaling molecule that plays a role in the development of inflammatory disorders. Nuclear factor erythroid2 related factor2 (Nrf2) is the main regulator of antioxidant cellular response to cell and tissue-destroying components caused by CS. Nrf2 protein that is significantly activated in the smokers' small airway epithelium is followed by a series of gene expression changes in the same cells. This study aims to observe differentially expressed genes (DEGs) in the human small airway epithelium of smokers compared to genes whose expression changes due to astaxanthin (AST) treatment, an antioxidant compound that can modulate Nrf2. Gene expression data that was stored in the GEO browser (GSE 11952) was analyzed using GEO2R to search for DEG among smokers and nonsmokers subject. DEG was further compared to those genes whose expression changes due to astaxanthin treatment (AST) that were obtained from the Comparative Toxicogenomics Database (CTD; https://ctdbase.org/). DEG (p < 0.05) analysis result shows that there are 23 genes whose expression regulation is reversed compared to gene expression due to AST treatment. The gene function annotations of the 23 DEGs showed the involvement of some of these genes in chemical and oxidative stress, reactive oxygen species (ROS), and apoptotic signaling pathways. All of the genes were involved/associated with chronic bronchitis, adenocarcinoma of the lung, non-small-cell lung carcinoma, carcinoma, small cell lung carcinoma, type 2 diabetes mellitus, emphysema, ischemic stroke, lung diseases, and inflammation. Thus, AST treatment for smokers could potentially decrease the development of ROS and oxidative stress that leads to inflammation and health risks associated with smoking.

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发文量
16
审稿时长
16 weeks
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