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dc.contributor.authorKoçak, Engin
dc.contributor.authorÇelebier, Mustafa
dc.contributor.authorHaznedaroglu, Ibrahim C.
dc.contributor.authorAltınöz, Sacide
dc.date.accessioned2021-06-03T09:00:38Z
dc.date.available2021-06-03T09:00:38Z
dc.date.issued2019
dc.identifier.issn2314-6133
dc.identifier.urihttp://dx.doi.org/10.1155/2019/5268031
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6556321/
dc.identifier.urihttp://hdl.handle.net/11655/24368
dc.description.abstractAnkaferd hemostat (ABS), a traditional herbal extract, is a hemostatic agent used for wound healing and bleeding treatment. A standardized form of plants contains many biomolecules. In recent years, previous studies have demonstrated the antineoplastic effect of ABS. In the present work, we focused on the mechanism of its antineoplastic effect over Caco-2 colon cancer cells. The LC/MS-based proteomics method was used to understand the effect of ABS at the protein level. The results were evaluated with gene ontology, protein interaction, and pathway analysis. As shown by our results, ABS altered glucose, fatty acids, and protein metabolism. Moreover, ABS affects the cell cycle machinery. Moreover, we found that ABS induced critical cancer target and suppressor proteins such as carboxyl-terminal hydrolase 1, 60S ribosomal protein L5, Tumor protein D52-like2, karyopherin alpha 2, and protein deglycase DJ-1. In conclusion, the proteomics results indicated that ABS affects various cancer targets and suppressor proteins. Moreover ABS has systematical effect on cell metabolism and cell cycle in Caco-2 cells, suggesting that it could be used as an antineoplastic agent.
dc.language.isoen
dc.relation.isversionof10.1155/2019/5268031
dc.rightsAttribution 4.0 United States
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleAnalysis Of The Antiproliferative Effect Of Ankaferd Hemostat On Caco-2 Colon Cancer Cells Via Lc/Ms Shotgun Proteomics Approach
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalBiomed Research International
dc.contributor.departmentAnalitik Kimya
dc.identifier.volume2019
dc.description.indexPubMed
dc.description.indexWoS
dc.description.indexScopus


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Attribution 4.0 United States
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