Overcoming adaptive resistance in mucoepidermoid carcinoma through inhibition of the IKK-β/IκBα/NFκB axis
dc.contributor.author | Wagner, Vivian Petersen | pt_BR |
dc.contributor.author | Martins, Marco Antonio Trevizani | pt_BR |
dc.contributor.author | Martins, Manoela Domingues | pt_BR |
dc.contributor.author | Warner, Kristy | pt_BR |
dc.contributor.author | Webber, Liana Preto | pt_BR |
dc.contributor.author | Squarize, Cristiane Helena | pt_BR |
dc.contributor.author | Nor, Jacques Eduardo | pt_BR |
dc.contributor.author | Castilho, Rogerio Moraes | pt_BR |
dc.date.accessioned | 2018-10-26T02:43:36Z | pt_BR |
dc.date.issued | 2016 | pt_BR |
dc.identifier.issn | 1949-2553 | pt_BR |
dc.identifier.uri | http://hdl.handle.net/10183/184008 | pt_BR |
dc.description.abstract | Patients with mucoepidermoid carcinoma (MEC) experience low survival rates and high morbidity following treatment, yet the intrinsic resistance of MEC cells to ionizing radiation (IR) and the mechanisms underlying acquired resistance remain unexplored. Herein, we demonstrated that low doses of IR intrinsically activated NFκB in resistant MEC cell lines. Moreover, resistance was significantly enhanced in IR-sensitive cell lines when NFκB pathway was stimulated. Pharmacological inhibition of the IKK-β/IκBα/ NFκB axis, using a single dose of FDA-approved Emetine, led to a striking sensitization of MEC cells to IR and a reduction in cancer stem cells. We achieved a major step towards better understanding the basic mechanisms involved in IR-adaptive resistance in MEC cell lines and how to efficiently overcome this critical problem. | en |
dc.format.mimetype | application/pdf | pt_BR |
dc.language.iso | eng | pt_BR |
dc.relation.ispartof | Oncotarget. Albany. Vol. 7, no. 45 (Nov. 2016), p. 73032-73044 | pt_BR |
dc.rights | Open Access | en |
dc.subject | Patologia bucal | pt_BR |
dc.subject | Neoplasias bucais | pt_BR |
dc.title | Overcoming adaptive resistance in mucoepidermoid carcinoma through inhibition of the IKK-β/IκBα/NFκB axis | pt_BR |
dc.type | Artigo de periódico | pt_BR |
dc.identifier.nrb | 001059514 | pt_BR |
dc.type.origin | Estrangeiro | pt_BR |
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