Potential therapeutic targets for COVID-19 complicated with pulmonary hypertension: a bioinformatics and early validation study

被引:0
作者
Hou, Qingbin [1 ]
Jiang, Jinping [2 ]
Na, Kun [1 ]
Zhang, Xiaolin [1 ]
Liu, Dan [1 ]
Jing, Quanmin [1 ]
Yan, Chenghui [1 ]
Han, Yaling [1 ]
机构
[1] Gen Hosp Northern Theater Command, Cardiovasc Res Inst, State Key Lab Frigid Zone Cardiovasc Dis, Dept Cardiol, Shenyang, Peoples R China
[2] China Med Univ, Shengjing Affiliated Hosp, Dept Cardiol, Shenyang, Peoples R China
来源
SCIENTIFIC REPORTS | 2024年 / 14卷 / 01期
基金
中国国家自然科学基金;
关键词
COVID-19; Pulmonary hypertension; Differentially expressed genes; Machine algorithms; Core gene; Immune invasion; Molecular docking; E-SELECTIN; IMMUNE-RESPONSE; DNA-DAMAGE; DISEASE; VIRUS; FENRETINIDE; POPULATION; METABOLISM; PROTEIN; LEVEL;
D O I
10.1038/s41598-024-60113-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Coronavirus disease (COVID-19) and pulmonary hypertension (PH) are closely correlated. However, the mechanism is still poorly understood. In this article, we analyzed the molecular action network driving the emergence of this event. Two datasets (GSE113439 and GSE147507) from the GEO database were used for the identification of differentially expressed genes (DEGs).Common DEGs were selected by VennDiagram and their enrichment in biological pathways was analyzed. Candidate gene biomarkers were selected using three different machine-learning algorithms (SVM-RFE, LASSO, RF).The diagnostic efficacy of these foundational genes was validated using independent datasets. Eventually, we validated molecular docking and medication prediction. We found 62 common DEGs, including several ones that could be enriched for Immune Response and Inflammation. Two DEGs (SELE and CCL20) could be identified by machine-learning algorithms. They performed well in diagnostic tests on independent datasets. In particular, we observed an upregulation of functions associated with the adaptive immune response, the leukocyte-lymphocyte-driven immunological response, and the proinflammatory response. Moreover, by ssGSEA, natural killer T cells, activated dendritic cells, activated CD4 T cells, neutrophils, and plasmacytoid dendritic cells were correlated with COVID-19 and PH, with SELE and CCL20 showing the strongest correlation with dendritic cells. Potential therapeutic compounds like FENRETI-NIDE, AFLATOXIN B1 and 1-nitropyrene were predicted. Further molecular docking and molecular dynamics simulations showed that 1-nitropyrene had the most stable binding with SELE and CCL20.The findings indicated that SELE and CCL20 were identified as novel diagnostic biomarkers for COVID-19 complicated with PH, and the target of these two key genes, FENRETI-NIDE and 1-nitropyrene, was predicted to be a potential therapeutic target, thus providing new insights into the prediction and treatment of COVID-19 complicated with PH in clinical practice.
引用
收藏
页数:19
相关论文
共 85 条
  • [1] COVID-19 pandemic: what's next for public health?
    不详
    [J]. LANCET PUBLIC HEALTH, 2022, 7 (05) : E391 - E391
  • [2] [Anonymous], 2021, LANCET, V398, P725, DOI 10.1016/S0140-6736(21)01900-0
  • [3] Meta-analysis on outcome-worsening comorbidities of COVID-19 and related potential drug-drug interactions
    Awortwe, Charles
    Cascorbi, Ingolf
    [J]. PHARMACOLOGICAL RESEARCH, 2020, 161
  • [4] Aflatoxin B1-induced DNA damage and its repair
    Bedard, Leanne L.
    Massey, Thomas E.
    [J]. CANCER LETTERS, 2006, 241 (02) : 174 - 183
  • [5] Between inflammation and thrombosis: endothelial cells in COVID-19
    Birnhuber, Anna
    Fliesser, Elisabeth
    Gorkiewicz, Gregor
    Zacharias, Martin
    Seeliger, Benjamin
    David, Sascha
    Welte, Tobias
    Schmidt, Julius
    Olschewski, Horst
    Wygrecka, Malgorzata
    Kwapiszewska, Grazyna
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2021, 58 (03)
  • [6] Efficient RMSD measures for the comparison of two molecular ensembles
    Brüschweiler, R
    [J]. PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2003, 50 (01) : 26 - 34
  • [7] Pulmonary Hypertension and COVID-19
    Castiglione, Laura
    Droppa, Michal
    [J]. HAMOSTASEOLOGIE, 2022, 42 (04): : 230 - 238
  • [8] Genome mining for lasso peptides: past, present, and future
    Cheung-Lee, Wai Ling
    Link, A. James
    [J]. JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, 2019, 46 (9-10) : 1371 - 1379
  • [9] Persistent alveolar inflammatory response in critically ill patients with COVID-19 is associated with mortality
    de Brabander, Justin
    Boers, Leonoor S.
    Kullberg, Robert F. J.
    Zhang, Shiqi
    Nossent, Esther J.
    Heunks, Leo M. A.
    Vlaar, Alexander P. J.
    Bonta, Peter, I
    Schultz, Marcus J.
    van der Poll, Tom
    Duitman, JanWillem
    Bos, Lieuwe D. J.
    [J]. THORAX, 2023, : 912 - 921
  • [10] Chronic thromboembolic pulmonary hypertension and clot resolution after COVID-19-associated pulmonary embolism
    de Jong, Cindy M. M.
    Visser, Chantal
    Bemelmans, Remy H. H.
    Boersma, Wim G.
    van den Borst, Bram
    Burggraaf, J. Louise I.
    Cannegieter, Suzanne C.
    ten Cate-Hoek, Arina J.
    Croles, F. Nanne
    Faber, Harald J.
    Faber, Laura M.
    Hellemons, Merel E.
    Hessels, Lisa M.
    Huisman, Menno, V
    Kamphuisen, Pieter W.
    Koster, Stephanie C. E.
    Kroft, Lucia J. M.
    van der Lee, Ivo
    Leentjens, Jenneke
    Meijer, Karina
    Ninaber, Maarten K.
    Sondermeijer, Brigitte M.
    Stads, Susanne
    Noordegraaf, Anton Vonk
    Winckers, Kristien
    Kruip, Marieke J. H. A.
    Klok, Frederikus A.
    [J]. EUROPEAN RESPIRATORY JOURNAL, 2023, 61 (04)