Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/9021
DC FieldValueLanguage
dc.contributor.authorBordón, Elisaen_US
dc.contributor.authorHenríquez Hernández, Luis Albertoen_US
dc.contributor.authorLara Jiménez, Pedro Carlosen_US
dc.contributor.authorRuiz Alonso, Anaen_US
dc.contributor.authorPinar, Beatrizen_US
dc.contributor.authorRodríguez-Gallego, Carlosen_US
dc.contributor.authorLloret Saez-Bravo, Martaen_US
dc.date.accessioned2012-11-15T09:12:40Z-
dc.date.accessioned2018-04-25T13:59:29Z-
dc.date.available2012-11-15T09:12:40Z-
dc.date.available2018-04-25T13:59:29Z-
dc.date.issued2010en_US
dc.identifier.issn1748-717Xen_US
dc.identifier.urihttp://hdl.handle.net/10553/9021-
dc.description.abstractHead and neck cancer is treated mainly by surgery and radiotherapy. Normal tissue toxicity due to x-ray exposure is a limiting factor for treatment success. Many efforts have been employed to develop predictive tests applied to clinical practice. Determination of lymphocyte radio-sensitivity by radio-induced apoptosis arises as a possible method to predict tissue toxicity due to radiotherapy. The aim of the present study was to analyze radio-induced apoptosis of peripheral blood lymphocytes in head and neck cancer patients and to explore their role in predicting radiation induced toxicity. Seventy nine consecutive patients suffering from head and neck cancer, diagnosed and treated in our institution, were included in the study. Toxicity was evaluated using the Radiation Therapy Oncology Group scale. Peripheral blood lymphocytes were isolated and irradiated at 0, 1, 2 and 8 Gy during 24 hours. Apoptosis was measured by flow cytometry using annexin V/propidium iodide. Lymphocytes were marked with CD45 APC-conjugated monoclonal antibody. Radiation-induced apoptosis increased in order to radiation dose and fitted to a semi logarithmic model defined by two constants: α and β. α, as the origin of the curve in the Y axis determining the percentage of spontaneous cell death, and β, as the slope of the curve determining the percentage of cell death induced at a determined radiation dose, were obtained. β value was statistically associated to normal tissue toxicity in terms of severe xerostomia, as higher levels of apoptosis were observed in patients with low toxicity (p = 0.035; Exp(B) 0.224, I.C.95% (0.060-0.904)). These data agree with our previous results and suggest that it is possible to estimate the radiosensitivity of peripheral blood lymphocytes from patients determining the radiation induced apoptosis with annexin V/propidium iodide staining. β values observed define an individual radiosensitivity profile that could predict late toxicity due to radiotherapy in locally advanced head and neck cancer patients. Anyhow, prospective studies with different cancer types and higher number of patients are needed to validate these results.en_US
dc.languageengen_US
dc.relation.ispartofRadiation Oncologyen_US
dc.sourceRadiation Oncology [ISSN 1748-717X], 2010, 5:4en_US
dc.subject320101 Oncologíaen_US
dc.subject.otherRadiation-Induced Apoptosis
dc.subject.otherRadiotherapy
dc.subject.otherAmifostine
dc.subject.otherRadiosensitivity
dc.subject.otherXerostomia
dc.subject.otherCarcinoma
dc.subject.otherTrial
dc.subject.otherCd4
dc.titlePrediction of clinical toxicity in locally advanced head and neck cancer patients by radio-induced apoptosis in peripheral blood lymphocytes (PBLs)en_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1186/1748-717X-5-4
dc.identifier.scopus2-s2.0-77249109445-
dc.identifier.isi000275041100001-
dc.date.updated2012-11-12T18:49:23Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066en-
dc.rights.holderElisa Bordón et al.; licensee BioMed Central Ltd.-
dc.compliance.driver1es
dc.identifier.crisid-;12688;325;-;21987;-;9308-
dc.investigacionCiencias de la Saluden_US
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess-
dc.rights.accessrightsinfo:eu-repo/semantics/openAccesses
dc.type2Artículoen_US
dc.contributor.daisngid2045042
dc.contributor.daisngid465624
dc.contributor.daisngid591076
dc.contributor.daisngid6269840
dc.contributor.daisngid1285881
dc.contributor.daisngid603384
dc.contributor.daisngid802813
dc.contributor.wosstandardWOS:Bordon, E
dc.contributor.wosstandardWOS:Henriquez-Hernandez, LA
dc.contributor.wosstandardWOS:Lara, PC
dc.contributor.wosstandardWOS:Ruiz, A
dc.contributor.wosstandardWOS:Pinar, B
dc.contributor.wosstandardWOS:Rodriguez-Gallego, C
dc.contributor.wosstandardWOS:Lloret, M
dc.date.coverdateEnero 2010
dc.identifier.ulpgces
dc.description.jcr2,409
dc.description.jcrqQ2
dc.description.scieSCIE
item.fulltextCon texto completo-
item.grantfulltextopen-
crisitem.author.deptGIR IUIBS: Medio Ambiente y Salud-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.deptGIR IUIBS: Farmacología Molecular y Traslacional-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.orcid0000-0003-3237-0316-
crisitem.author.orcid0000-0002-4344-8644-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameBordón Rodríguez, Elisa de los Reyes-
crisitem.author.fullNameHenríquez Hernández, Luis Alberto-
crisitem.author.fullNameLara Jiménez, Pedro Carlos-
crisitem.author.fullNamePinar Sedeño, María Beatriz-
crisitem.author.fullNameRodríguez Gallego, José Carlos-
crisitem.author.fullNameLloret Sáez-Bravo, Marta-
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