Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/109889
PIRA download icon_1.1View/Download Full Text
DC FieldValueLanguage
dc.contributorDepartment of Food Science and Nutrition-
dc.contributorResearch Centre for Chinese Medicine Innovation-
dc.creatorGong, RH-
dc.creatorChen, JW-
dc.creatorShen, LS-
dc.creatorLin, YS-
dc.creatorYu, H-
dc.creatorChen, S-
dc.creatorChen, GQ-
dc.date.accessioned2024-11-20T07:30:11Z-
dc.date.available2024-11-20T07:30:11Z-
dc.identifier.issn1756-4646-
dc.identifier.urihttp://hdl.handle.net/10397/109889-
dc.language.isoenen_US
dc.publisherElsevier BVen_US
dc.rights© 2024 The Author(s). Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication Gong, R.-H., Chen, J.-W., Shen, L.-S., Lin, Y.-S., Yu, H., Chen, S., & Chen, G.-Q. (2024). Assessing the therapeutic potential of Elephantopus scaber extract in hepatocellular carcinoma by inhibiting the PI3K/Akt pathway. Journal of Functional Foods, 113, 106009 is available at https://doi.org/10.1016/j.jff.2024.106009.en_US
dc.subjectApoptosisen_US
dc.subjectCell cycleen_US
dc.subjectElephantopus scaberen_US
dc.subjectHepatocellular carcinomaen_US
dc.subjectMetastasisen_US
dc.subjectPI3K/Akt pathwayen_US
dc.titleAssessing the therapeutic potential of Elephantopus scaber extract in hepatocellular carcinoma by inhibiting the PI3K/Akt pathwayen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume113-
dc.identifier.doi10.1016/j.jff.2024.106009-
dcterms.abstractElephantopus scaber, globally acknowledged for its edible and medicinal uses, remains underexplored despite the identification of active compounds. This research explores Elephantopus scaber extract's therapeutic capabilities in hepatocellular carcinoma (HCC). Initial in vitro screenings using the MTT assay revealed that ethanol extract (EEES) inhibited HCC cell proliferation while exhibiting low toxicity to normal cells. Further explorations showed EEES induced cell cycle arrest, apoptosis, and inhibited cell metastasis. A bioinformatics analysis using a network pharmacology approach identified the PI3K/Akt pathway as a key modulation for EEES's anti-HCC activities, validated through western blot analysis. In animal studies, EEES demonstrated the ability to inhibit HCC tumor growth in vivo with a high level of safety. In summary, our research positions Elephantopus scaber as a potent herb with anti-HCC activities and remarkable safety, offering promising prospects for the prevention and treatment of liver diseases, including HCC.-
dcterms.abstractGraphical abstract: [Figure not available: see fulltext.]-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of functional foods, Feb. 2024, v. 113, 106009-
dcterms.isPartOfJournal of functional foods-
dcterms.issued2024-02-
dc.identifier.scopus2-s2.0-85182170718-
dc.identifier.eissn2214-9414-
dc.identifier.artn106009-
dc.description.validate202411 bcch-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextInnovation and Technology Fund- Mainland-Hong Kong Joint Funding Scheme; Shenzhen Science and Technology Innovation Commission; Research Centre for Chinese Medicine Innovation of The Hong Kong Polytechnic University; Hong Kong Polytechnic University Shenzhen Research Institute Life Science Research Start-up Funden_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
Appears in Collections:Journal/Magazine Article
Files in This Item:
File Description SizeFormat 
1-s2.0-S1756464624000112-main.pdf19.7 MBAdobe PDFView/Open
Open Access Information
Status open access
File Version Version of Record
Access
View full-text via PolyU eLinks SFX Query
Show simple item record

Page views

3
Citations as of Nov 24, 2024

Downloads

3
Citations as of Nov 24, 2024

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.