Immunoregulatory mechanism studies of ginseng leaves on lung cancer based on network pharmacology and molecular docking

Abstract Panax ginseng is one of the oldest and most generally prescribed herbs in Eastern traditional medicine to treat diseases. Several studies had documented that ginseng leaves have anti-oxidative, anti-inflammatory, and anticancer properties similar to those of ginseng root. The aim of this re...

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Autores principales: Zao-Hui Li, Dan Yu, Nan-Nan Huang, Jun-Kai Wu, Xiao-Wei Du, Xi-Jun Wang
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/b9f2d8584a9d4f9d9765582254efdde7
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spelling oai:doaj.org-article:b9f2d8584a9d4f9d9765582254efdde72021-12-02T15:16:05ZImmunoregulatory mechanism studies of ginseng leaves on lung cancer based on network pharmacology and molecular docking10.1038/s41598-021-97115-82045-2322https://doaj.org/article/b9f2d8584a9d4f9d9765582254efdde72021-09-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-97115-8https://doaj.org/toc/2045-2322Abstract Panax ginseng is one of the oldest and most generally prescribed herbs in Eastern traditional medicine to treat diseases. Several studies had documented that ginseng leaves have anti-oxidative, anti-inflammatory, and anticancer properties similar to those of ginseng root. The aim of this research was to forecast of the molecular mechanism of ginseng leaves on lung cancer by molecular docking and network pharmacology so as to decipher ginseng leaves' entire mechanism. The compounds associated with ginseng leaves were searched by TCMSP. TCMSP and Swiss Target Prediction databases were used to sort out the potential targets of the main chemical components. Targets were collected from OMIM, PharmGKB, TTD, DrugBank and GeneCards which related to immunity and lung cancer. Ginseng leaves exert its lung cancer suppressive function by regulating the several signaling proteins, such as JUN, STAT3, AKT1, TNF, MAPK1, TP53. GO and KEGG analyses indicated that the immunoreaction against lung cancer by ginseng leaves might be related to response to lipopolysaccharide, response to oxidative stress, PI3K-Akt, MAPK and TNF pathway. Molecular docking analysis demonstrated that hydrogen bonding was interaction's core forms. The results of CCK8 test and qRT-PCR showed that ginseng leaves inhibit cell proliferation and regulates AKT1 and P53 expression in A549. The present study clarifies the mechanism of Ginseng leaves against lung cancer and provides evidence to support its clinical use.Zao-Hui LiDan YuNan-Nan HuangJun-Kai WuXiao-Wei DuXi-Jun WangNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Zao-Hui Li
Dan Yu
Nan-Nan Huang
Jun-Kai Wu
Xiao-Wei Du
Xi-Jun Wang
Immunoregulatory mechanism studies of ginseng leaves on lung cancer based on network pharmacology and molecular docking
description Abstract Panax ginseng is one of the oldest and most generally prescribed herbs in Eastern traditional medicine to treat diseases. Several studies had documented that ginseng leaves have anti-oxidative, anti-inflammatory, and anticancer properties similar to those of ginseng root. The aim of this research was to forecast of the molecular mechanism of ginseng leaves on lung cancer by molecular docking and network pharmacology so as to decipher ginseng leaves' entire mechanism. The compounds associated with ginseng leaves were searched by TCMSP. TCMSP and Swiss Target Prediction databases were used to sort out the potential targets of the main chemical components. Targets were collected from OMIM, PharmGKB, TTD, DrugBank and GeneCards which related to immunity and lung cancer. Ginseng leaves exert its lung cancer suppressive function by regulating the several signaling proteins, such as JUN, STAT3, AKT1, TNF, MAPK1, TP53. GO and KEGG analyses indicated that the immunoreaction against lung cancer by ginseng leaves might be related to response to lipopolysaccharide, response to oxidative stress, PI3K-Akt, MAPK and TNF pathway. Molecular docking analysis demonstrated that hydrogen bonding was interaction's core forms. The results of CCK8 test and qRT-PCR showed that ginseng leaves inhibit cell proliferation and regulates AKT1 and P53 expression in A549. The present study clarifies the mechanism of Ginseng leaves against lung cancer and provides evidence to support its clinical use.
format article
author Zao-Hui Li
Dan Yu
Nan-Nan Huang
Jun-Kai Wu
Xiao-Wei Du
Xi-Jun Wang
author_facet Zao-Hui Li
Dan Yu
Nan-Nan Huang
Jun-Kai Wu
Xiao-Wei Du
Xi-Jun Wang
author_sort Zao-Hui Li
title Immunoregulatory mechanism studies of ginseng leaves on lung cancer based on network pharmacology and molecular docking
title_short Immunoregulatory mechanism studies of ginseng leaves on lung cancer based on network pharmacology and molecular docking
title_full Immunoregulatory mechanism studies of ginseng leaves on lung cancer based on network pharmacology and molecular docking
title_fullStr Immunoregulatory mechanism studies of ginseng leaves on lung cancer based on network pharmacology and molecular docking
title_full_unstemmed Immunoregulatory mechanism studies of ginseng leaves on lung cancer based on network pharmacology and molecular docking
title_sort immunoregulatory mechanism studies of ginseng leaves on lung cancer based on network pharmacology and molecular docking
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/b9f2d8584a9d4f9d9765582254efdde7
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