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dc.contributor.authorAryappalli, Priyanka
dc.contributor.authorShabbiri, Khadija
dc.contributor.authorMasad, Razan J.
dc.contributor.authorAl-Marri, Roadha H.
dc.contributor.authorHaneefa, Shoja M.
dc.contributor.authorMohamed, Yassir A.
dc.contributor.authorArafat, Kholoud
dc.contributor.authorAttoub, Samir
dc.contributor.authorCabral-Marques, Otavio
dc.contributor.authorRamadi, Khalil
dc.contributor.authorFernandez-Cabezudo, Maria J.
dc.contributor.authoral-Ramadi, Basel K.
dc.date.accessioned2020-05-21T19:16:51Z
dc.date.available2020-05-21T19:16:51Z
dc.date.issued2019-09-05
dc.date.submitted2019-07
dc.identifier.issn1422-0067
dc.identifier.urihttps://hdl.handle.net/1721.1/125388
dc.description.abstractAberrantly high levels of tyrosine-phosphorylated signal transducer and activator of transcription 3 (p-STAT3) are found constitutively in ~50% of human lung and breast cancers, acting as an oncogenic transcription factor. We previously demonstrated that Manuka honey (MH) inhibits p-STAT3 in breast cancer cells, but the exact mechanism remained unknown. Herein, we show that MH-mediated inhibition of p-STAT3 in breast (MDA-MB-231) and lung (A549) cancer cell lines is accompanied by decreased levels of gp130 and p-JAK2, two upstream components of the IL-6 receptor (IL-6R) signaling pathway. Using an ELISA-based assay, we demonstrate that MH binds directly to IL-6R&alpha;, significantly inhibiting (~60%) its binding to the IL-6 ligand. Importantly, no evidence of MH binding to two other cytokine receptors, IL-11R&alpha; and IL-8R, was found. Moreover, MH did not alter the levels of tyrosine-phosphorylated or total Src family kinases, which are also constitutively activated in cancer cells, suggesting that signaling via other growth factor receptors is unaffected by MH. Binding of five major MH flavonoids (luteolin, quercetin, galangin, pinocembrin, and chrysin) was also tested, and all but pinocembrin could demonstrably bind IL-6R&alpha;, partially (30&ndash;35%) blocking IL-6 binding at the highest concentration (50 &mu;M) used. In agreement, each flavonoid inhibited p-STAT3 in a dose-dependent manner, with estimated IC<sub>50</sub> values in the 3.5&ndash;70 &mu;M range. Finally, docking analysis confirmed the capacity of each flavonoid to bind in an energetically favorable configuration to IL-6R&alpha; at a site predicted to interfere with ligand binding. Taken together, our findings identify IL-6R&alpha; as a direct target of MH and its flavonoids, highlighting IL-6R blockade as a mechanism for the anti-tumor activity of MH, as well as a viable therapeutic target in IL-6-dependent cancers. Keywords: Manuka honey; Flavonoids; IL-6 receptor; STAT3; IL-6; breast and lung cancersen_US
dc.description.sponsorshipZayed Center for Health Sciences (grant no. 31R025)en_US
dc.description.sponsorshipUAEU Program for Advanced Research (grant no. 31M409)en_US
dc.publisherMultidisciplinary Digital Publishing Instituteen_US
dc.relation.isversionof10.3390/ijms20184340en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceMultidisciplinary Digital Publishing Instituteen_US
dc.titleInhibition of tyrosine-phosphorylated STAT3 in human breast and lung cancer cells by Manuka honey is mediated by selective antagonism of the IL-6 receptoren_US
dc.typeArticleen_US
dc.identifier.citationAryappalli, Priyanka, et al., "Inhibition of tyrosine-phosphorylated STAT3 in human breast and lung cancer cells by Manuka honey is mediated by selective antagonism of the IL-6 receptor." International Journal of Molecular Sciences 20, 18 (Sept. 2019): no. 4340 doi 10.3390/ijms20184340 ©2019 Author(s)en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.relation.journalInternational Journal of Molecular Sciencesen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-03-02T12:56:00Z
dspace.date.submission2020-03-02T12:56:00Z
mit.journal.volume20en_US
mit.journal.issue18en_US
mit.licensePUBLISHER_CC
mit.metadata.statusComplete


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