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    標題: Novel signaling pathways regulate SARS-CoV and SARS-CoV-2 infectious disease
    作者: Cheng, Li-Chin
    Kao, Tzu-Jen
    Phan, Nam Nhut
    Chiao, Chung-Chieh
    Yen, Meng-Chi
    Chen, Chien-Fu
    Hung, Jui-Hsiang
    Jiang, Jia-Zhen
    Sun, Zhengda
    Wang, Chih-Yang
    Hsu, Hui-Ping
    貢獻者: Chi Mei Med Ctr, Dept Surg, Div Colorectal Surg
    Taipei Med Univ, Coll Med Sci & Technol, PhD Program Neural Regenerat Med
    Natl Hlth Res Inst
    Taipei Med Univ, TMU Res Ctr Neurosci
    Nguyen Tat Thanh NTT Univ, NTT Inst Hitechnol
    I Shou Univ, Sch Chinese Med Postbaccalaureate
    Kaohsiung Med Univ Hosp, Dept Emergency Med
    Kaohsiung Med Univ, Coll Med, Grad Inst Clin Med
    Chia Nan Univ Pharm & Sci, Dept Biotechnol
    Fudan Univ, Huashan Hosp North, Emergency Dept
    Kaiser Permanente, Northern Calif Reg Labs, Permanente Med Grp
    Taipei Med Univ, PhD Program Canc Mol Biol & Drug Discovery, Coll Med Sci & Technol
    Taipei Med Univ, Coll Med Sci & Technol, Grad Inst Canc Biol & Drug Discovery
    Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Surg, Tainan, Taiwan;[Hsu, Hui-Ping
    Vanderbilt Univ, Med Ctr, Dept Biostat
    關鍵字: bioinformatics
    coronavirus
    interleukin-17
    severe acute respiratory syndrome coronavirus
    severe acute respiratory syndrome coronavirus-2
    tumor necrosis factor
    日期: 2021
    上傳時間: 2023-11-11 11:55:32 (UTC+8)
    出版者: LIPPINCOTT WILLIAMS & WILKINS
    摘要: Severe acute respiratory syndrome coronavirus (SARS-CoV)-2 induces severe infection, and it is responsible for a worldwide disease outbreak starting in late 2019. Currently, there are no effective medications against coronavirus. In the present study, we utilized a holistic bioinformatics approach to study gene signatures of SARS-CoV- and SARS-CoV-2-infected Calu-3 lung adenocarcinoma cells. Through the Gene Ontology platform, we determined that several cytokine genes were up-regulated after SARS-CoV-2 infection, including TNF, IL6, CSF2, IFNL1, IL-17C, CXCL10, and CXCL11. Differentially regulated pathways were detected by the Kyoto Encyclopedia of Genes and Genomes, gene ontology, and Hallmark platform, including chemokines, cytokines, cytokine receptors, cytokine metabolism, inflammation, immune responses, and cellular responses to the virus. A Venn diagram was utilized to illustrate common overlapping genes from SARS-CoV- and SARS-CoV-2-infected datasets. An Ingenuity pathway analysis discovered an enrichment of tumor necrosis factor- (TNF-) and interleukin (IL)-17-related signaling in a gene set enrichment analysis. Downstream networks were predicted by the Database for Annotation, Visualization, and Integrated Discovery platform also revealed that TNF and TNF receptor 2 signaling elicited leukocyte recruitment, activation, and survival of host cells after coronavirus infection. Our discovery provides essential evidence for transcript regulation and downstream signaling of SARS-CoV and SARS-CoV-2 infection.
    關聯: MEDICINE, v.100, n.7, e24321
    顯示於類別:[生物科技系(所)] 期刊論文

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