Systems pharmacology-based drug discovery and active mechanism of natural products for coronavirus pneumonia (COVID-19): An example using flavonoids

被引:21
作者
Wang, Bin [1 ]
Ding, Yan [1 ]
Zhao, Penghui [1 ]
Li, Wei [2 ]
Li, Ming [3 ]
Zhu, Jingbo [1 ,4 ]
Ye, Shuhong [1 ]
机构
[1] Dalian Polytech Univ, Sch Food Sci & Technol, Dalian 116034, Liaoning, Peoples R China
[2] Korea Inst Oriental Med, Korean Med KM Applicat Ctr, Daegu 41062, South Korea
[3] Dalian Med Univ, Coll Basic Med Sci, Dalian 116044, Liaoning, Peoples R China
[4] Dalian Polytech Univ, Inst Chem & Applicat Plant Resources, Dalian 116034, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
Systems pharmacology; Natural products; Flavonoids; COVID-19; Molecular docking; NETWORK PHARMACOLOGY; PLANT FLAVONOIDS; GENE ONTOLOGY; IN-VITRO; INHIBITORS; CELLS; POLYPHENOLS; PREDICTION; QUERCETIN; CYTOSCAPE;
D O I
10.1016/j.compbiomed.2022.105241
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Recently, the value of natural products has been extensively considered because these resources can potentially be applied to prevent and treat coronavirus pneumonia 2019 (COVID-19). However, the discovery of nature drugs is problematic because of their complex composition and active mechanisms.Methods: This comprehensive study was performed on flavonoids, which are compounds with anti-inflammatory and antiviral effects, to show drug discovery and active mechanism from natural products in the treatment of COVID-19 via a systems pharmacological model. First, a chemical library of 255 potential flavonoids was constructed. Second, the pharmacodynamic basis and mechanism of action between flavonoids and COVID-19 were explored by constructing a compound-target and target-disease network, targets protein-protein interaction (PPI), MCODE analysis, gene ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment.Results: In total, 105 active flavonoid components were identified, of which 6 were major candidate compounds (quercetin, epigallocatechin-3-gallate (EGCG), luteolin, fisetin, wogonin, and licochalcone A). 152 associated targets were yielded based on network construction, and 7 family proteins (PTGS, GSK3 beta, ABC, NOS, EGFR, and IL) were included as central hub targets. Moreover, 528 GO items and 178 KEGG pathways were selected through enrichment of target functions. Lastly, molecular docking demonstrated good stability of the combination of selected flavonoids with 3CL Pro and ACEII.Conclusion: Natural flavonoids could enable resistance against COVID-19 by regulating inflammatory, antiviral, and immune responses, and repairing tissue injury. This study has scientific significance for the selective utilization of natural products, medicinal value enhancement of flavonoids, and drug screening for the treatment of COVID-19 induced by SARS-COV-2.
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页数:14
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共 91 条
  • [1] Natural products' role against COVID-19
    Antonio, Ananda da Silva
    Moreira Wiedemann, Larissa Silveira
    Veiga-Junior, Valdir Florencio
    [J]. RSC ADVANCES, 2020, 10 (39) : 23379 - 23393
  • [2] Gene Ontology: tool for the unification of biology
    Ashburner, M
    Ball, CA
    Blake, JA
    Botstein, D
    Butler, H
    Cherry, JM
    Davis, AP
    Dolinski, K
    Dwight, SS
    Eppig, JT
    Harris, MA
    Hill, DP
    Issel-Tarver, L
    Kasarskis, A
    Lewis, S
    Matese, JC
    Richardson, JE
    Ringwald, M
    Rubin, GM
    Sherlock, G
    [J]. NATURE GENETICS, 2000, 25 (01) : 25 - 29
  • [3] An automated method for finding molecular complexes in large protein interaction networks
    Bader, GD
    Hogue, CW
    [J]. BMC BIOINFORMATICS, 2003, 4 (1)
  • [4] Multi-omits-based identification of SARS-CoV-2 infection biology and candidate drugs against COVID-19
    Barh, Debmalya
    Tiwari, Sandeep
    Weener, Marianna E.
    Azevedo, Vasco
    Goes-Neto, Aristoteles
    Gromiha, M. Michael
    Ghosh, Preetam
    [J]. COMPUTERS IN BIOLOGY AND MEDICINE, 2020, 126
  • [5] Untitled
    Bateman, Alex
    [J]. NUCLEIC ACIDS RESEARCH, 2006, 34 : D1 - D1
  • [6] The Protein Data Bank
    Berman, HM
    Westbrook, J
    Feng, Z
    Gilliland, G
    Bhat, TN
    Weissig, H
    Shindyalov, IN
    Bourne, PE
    [J]. NUCLEIC ACIDS RESEARCH, 2000, 28 (01) : 235 - 242
  • [7] ClueGO: a Cytoscape plug-in to decipher functionally grouped gene ontology and pathway annotation networks
    Bindea, Gabriela
    Mlecnik, Bernhard
    Hackl, Hubert
    Charoentong, Pornpimol
    Tosolini, Marie
    Kirilovsky, Amos
    Fridman, Wolf-Herman
    Pages, Franck
    Trajanoski, Zlatko
    Galon, Jerome
    [J]. BIOINFORMATICS, 2009, 25 (08) : 1091 - 1093
  • [8] Dietary agents in cancer prevention: flavonoids and isoflavonoids
    Birt, DF
    Hendrich, S
    Wang, WQ
    [J]. PHARMACOLOGY & THERAPEUTICS, 2001, 90 (2-3) : 157 - 177
  • [9] Effect of High vs Low Doses of Chloroquine Diphosphate as Adjunctive Therapy for Patients Hospitalized With Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection A Randomized Clinical Trial
    Borba, Mayla Gabriela Silva
    Val, Fernando Fonseca Almeida
    Sampaio, Vanderson Souza
    Alexandre, Marcia Almeida Araujo
    Melo, Gisely Cardoso
    Brito, Marcelo
    Mourao, Maria Paula Gomes
    Brito-Sousa, Jose Diego
    Baia-da-Silva, Djane
    Guerra, Marcus Vinitius Farias
    Hajjar, Ludhmila Abrahao
    Pinto, Rosemary Costa
    Balieiro, Antonio Alcirley Silva
    Pacheco, Antonio Guilherme Fonseca
    Santos, James Dean Oliveira, Jr.
    Naveca, Felipe Gomes
    Xavier, Mariana Simao
    Siqueira, Andre Machado
    Schwarzbold, Alexandre
    Croda, Julio
    Nogueira, Mauricio Lacerda
    Romero, Gustavo Adolfo Sierra
    Bassat, Quique
    Fontes, Cor Jesus
    Albuquerque, Bernardino Claudio
    Daniel-Ribeiro, Claudio-Tadeu
    Monteiro, Wuelton Marcelo
    Lacerda, Marcus Vinicius Guimaraes
    [J]. JAMA NETWORK OPEN, 2020, 3 (04) : E208857
  • [10] Antithrombotic Activities of Luteolin In Vitro and In Vivo
    Choi, Jun-Hui
    Kim, Yoon-Sik
    Shin, Chang-Ho
    Lee, Hyo-Jeong
    Kim, Seung
    [J]. JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2015, 29 (12) : 552 - 558