Publication:
TOX Expression in Mycosis Fungoides and Sezary Syndrome.

dc.contributor.authorPileri, Alessandro
dc.contributor.authorCavicchi, Martina
dc.contributor.authorBertuzzi, Clara
dc.contributor.authorRighi, Simona
dc.contributor.authorZengarini, Corrado
dc.contributor.authorSabattini, Elena
dc.contributor.authorRoncador, Giovanna
dc.contributor.authorAgostinelli, Claudio
dc.date.accessioned2023-06-07T11:46:33Z
dc.date.available2023-06-07T11:46:33Z
dc.date.issued2022-06-29
dc.description.abstractMycosis fungoides (MF) and Sezary syndrome (SS) are the two most common type of cutaneous T-cell lymphoma (CTCL). Currently, no markers can be clearly related to prognosis or to differential diagnosis between early stages and inflammatory benign diseases (IBD). The thymocyte selection-associated high mobility group box factor (TOX), has been proposed as a possible marker in differential diagnosis between early CTCL stages and IBD. Recently TOX has been related to prognosis. We aimed to investigate whether TOX may be a diagnostic or prognostic marker. MF and SS biopsies between 2010 and 2020 were retrieved. New tissues slides were stained with an anti-TOX antibody, (Clone NAN448B). On each slide, 5 fields were examined at high magnification (400×), to evaluate the percentage of marker-positivity in a quantitative way. Thirty-six patients (12 females and 24 males) and 48 biopsies were collected. Nine patients had multiple biopsies. TOX expression in MF/SS cases showed an increase from early to advanced phases. TOX was not regarded as a prognostic marker due to the absence of significant changes by comparing early MF cases with reactive conditions. TOX statistical significance increased in patients alive with disease and in those dead of disease (p = 0.013 and = 0.0005, respectively) as compared with patients in complete remission. Our results show that TOX should be regarded more as a prognostic than a diagnostic marker.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis research received no external fundinges_ES
dc.format.number7es_ES
dc.format.page1582es_ES
dc.format.volume12es_ES
dc.identifier.citationDiagnostics (Basel) . 2022;12(7):1582es_ES
dc.identifier.doi10.3390/diagnostics12071582es_ES
dc.identifier.issn2075-4418es_ES
dc.identifier.journalDiagnostics (Basel, Switzerland)es_ES
dc.identifier.pubmedID35885488es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/16155
dc.language.isoenges_ES
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.relation.publisherversionhttps://doi.org/10.3390/diagnostics12071582.es_ES
dc.repisalud.institucionCNIOes_ES
dc.repisalud.orgCNIOCNIO::Unidades técnicas::Unidad de Anticuerpos Monoclonaleses_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución-NoComercial-CompartirIgual 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.subjectTOXes_ES
dc.subjectMYCOSIS FUNGOIDESes_ES
dc.subjectSEZARY SYNDROMEes_ES
dc.titleTOX Expression in Mycosis Fungoides and Sezary Syndrome.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublicationed512382-68d2-4ded-b890-b84f9140f38c
relation.isAuthorOfPublication.latestForDiscoveryed512382-68d2-4ded-b890-b84f9140f38c
relation.isPublisherOfPublication30293a55-0e53-431f-ae8c-14ab01127be9
relation.isPublisherOfPublication.latestForDiscovery30293a55-0e53-431f-ae8c-14ab01127be9

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