Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/12649
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dc.contributor.authorKashyap, Dharmendraen_US
dc.contributor.authorRoy, Rajarshien_US
dc.contributor.authorVarshney, Nidhien_US
dc.contributor.authorBaral, Budhadeven_US
dc.contributor.authorBagde, Pranit Hemanten_US
dc.contributor.authorKandpal, Meenakshien_US
dc.contributor.authorKar, Parimalen_US
dc.contributor.authorJha, Hem Chandraen_US
dc.date.accessioned2023-12-14T12:38:05Z-
dc.date.available2023-12-14T12:38:05Z-
dc.date.issued2023-
dc.identifier.citationKashyap, D., Roy, R., Varshney, N., Baral, B., Bagde, P. H., Kandpal, M., Kumar, S., Kar, P., & Jha, H. C. (2023). Withania somnifera extract reduces gastric cancerous properties through inhibition of gankyrin in cellular milieu produced by Helicobacter pylori and Epstein Barr virus. Journal of Biomolecular Structure and Dynamics. Scopus. https://doi.org/10.1080/07391102.2023.2252096en_US
dc.identifier.issn0739-1102-
dc.identifier.otherEID(2-s2.0-85169585648)-
dc.identifier.urihttps://doi.org/10.1080/07391102.2023.2252096-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/12649-
dc.description.abstractHelicobacter pylori and Epstein Barr virus (EBV) are group1 carcinogens and their role in Gastric cancer (GC) is well established. Previously we have shown that H. pylori and EBV appears to support aggressive gastric oncogenesis through the upregulation of oncoprotein Gankyrin. Natural plant active molecules have the potential to interrupt oncogenesis. Herein, we investigated the potential of Withania somnifera root extract (WSE) as a possible chemotherapeutic agent against host oncoprotein Gankyrin whose expression was altered by H. pylori and EBV-associated modified cellular milieu. The results show that WSE does not have any inhibitory effect on H. pylori and EBV-associated gene transcripts except for the lmps (lmp1, lmp2a, and lmp2B). Moreover, the WSE exert their anticancer activity via host cellular response and decreased the expression of cell-migratory (mmp3 and mmp7)en_US
dc.description.abstractcell-cycle regulator (pcna)en_US
dc.description.abstractantiapoptotic gene (bcl2)en_US
dc.description.abstractincreased the expression of the proapoptotic gene (apaf1 and bax)en_US
dc.description.abstractand tumor suppressor (p53, prb, and pten). Knockdown of Gankyrin followed by the treatment of WSE also decreases the expression of TNF-ɑ, Akt, and elevated the expression of NFkB, PARP, Casp3, and Casp9. WSE also reduces cell migration, and genomic instability and forced the cells to commit programmed cell death. Moreover, molecular simulation studies revealed that out of eight active compounds of WSE, only four compounds such as withaferin A (WFA), withanoside IV (WA4), withanolide B (WNB), and withanolide D (WND) showed direct stable interaction with Gankyrin. This article reports for the first time that treatment of WSE decreased the cancerous properties through host cellular response modulation in gastric epithelial cells coinfected with H. pylori and EBV. Communicated by Ramaswamy H. Sarma. © 2023 Informa UK Limited, trading as Taylor & Francis Group.en_US
dc.language.isoenen_US
dc.publisherTaylor and Francis Ltd.en_US
dc.sourceJournal of Biomolecular Structure and Dynamicsen_US
dc.subjectcell signalingen_US
dc.subjectCo-infectionen_US
dc.subjectEBVen_US
dc.subjectgankyrinen_US
dc.subjectHelicobacter pylorien_US
dc.subjectwithania somniferaen_US
dc.titleWithania somnifera extract reduces gastric cancerous properties through inhibition of gankyrin in cellular milieu produced by Helicobacter pylori and Epstein Barr virusen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Biosciences and Biomedical Engineering

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