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基因毒性应激诱导内皮功能障碍中关键基因和通路的鉴定:全转录组测序结果

Identification of Key Genes and Pathways in Genotoxic Stress Induced Endothelial Dysfunction: Results of Whole Transcriptome Sequencing.

作者信息

Sinitsky Maxim, Sinitskaya Anna, Shishkova Daria, Tupikin Alexey, Asanov Maxim, Khutornaya Maria, Kabilov Marsel, Ponasenko Anastasia

机构信息

Laboratory of Genome Medicine, Research Institute for Complex Issues of Cardiovascular Diseases, 650002 Kemerovo, Russia.

Laboratory for Molecular, Translation and Digital Medicine, Research Institute for Complex Issues of Cardiovascular Diseases, 650002 Kemerovo, Russia.

出版信息

Biomedicines. 2022 Aug 24;10(9):2067. doi: 10.3390/biomedicines10092067.

Abstract

Atherosclerosis is a leading cause of cardiovascular morbidity and mortality worldwide. Endothelial disfunction underlying the atherogenesis can be triggered by genotoxic stress in endothelial cells. In the presented research whole transcriptome sequencing (RNA-seq) of human coronary artery (HCAEC) and internal thoracic artery (HITAEC) endothelial cells in vitro exposed to 500 ng/mL mitomycin C (treatment group) or 0.9% NaCl (control group) was performed. Resulting to bioinformatic analysis, 56 upregulated differentially expressed genes (DEGs) and 6 downregulated DEGs with absolute fold change ≥ 2 and FDR p-value < 0.05 were selected in HCAEC exposed to mitomycin C compared to the control group; in HITAEC only one upregulated DEG was found. According to Gene Ontology enrichment analysis, DEGs in HCAEC were classified into 25 functional groups of biological processes, while in HITAEC we found no statistically significant (FDR p-value < 0.05) groups. The four largest groups containing more than 50% DEGs (“signal transduction”, “response to stimulus”, “biological regulation”, and “regulation of biological process”) were identified. Finally, candidate DEGs and pathways underlying the genotoxic stress induced endothelial disfunction have been discovered that could improve our understanding of fundamental basis of atherogenesis and help to justification of genotoxic stress as a novel risk factor for atherosclerosis.

摘要

动脉粥样硬化是全球心血管疾病发病和死亡的主要原因。动脉粥样硬化发生过程中潜在的内皮功能障碍可由内皮细胞中的基因毒性应激引发。在本研究中,对体外暴露于500 ng/mL丝裂霉素C(治疗组)或0.9% NaCl(对照组)的人冠状动脉(HCAEC)和胸廓内动脉(HITAEC)内皮细胞进行了全转录组测序(RNA-seq)。经过生物信息学分析,与对照组相比,在暴露于丝裂霉素C的HCAEC中选择了56个上调的差异表达基因(DEG)和6个下调的DEG,其绝对变化倍数≥2且FDR p值<0.05;在HITAEC中仅发现1个上调的DEG。根据基因本体富集分析,HCAEC中的DEG被分为25个生物过程功能组,而在HITAEC中未发现具有统计学意义(FDR p值<0.05)的组。确定了包含超过50% DEG的四个最大组(“信号转导”、“对刺激的反应”、“生物调节”和“生物过程的调节”)。最后,发现了基因毒性应激诱导内皮功能障碍的候选DEG和途径,这可能会增进我们对动脉粥样硬化基本基础的理解,并有助于将基因毒性应激作为动脉粥样硬化的一种新危险因素进行论证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a65c/9495888/e21fd40708a3/biomedicines-10-02067-g001.jpg

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