TOX Expression in Mycosis Fungoides and Sezary Syndrome

被引:4
|
作者
Pileri, Alessandro [1 ,2 ]
Cavicchi, Martina [3 ]
Bertuzzi, Clara [4 ,5 ]
Righi, Simona [4 ,5 ]
Zengarini, Corrado [1 ,2 ]
Sabattini, Elena [4 ,5 ]
Roncador, Giovanna [6 ]
Agostinelli, Claudio [4 ,5 ]
机构
[1] IRCCS Policlin SantOrsola, Dermatol Unit, I-40138 Bologna, Italy
[2] Univ Bologna, Dept Expt Diagnost & Specially Med, Dermatol Unit, I-40138 Bologna, Italy
[3] Univ Modena & Reggio Emilia, Dept Dermatol, I-41121 Modena, Italy
[4] IRCCS Policlin SantOrsola, Hemathopathol Unit, I-40138 Bologna, Italy
[5] Univ Bologna, S Orsola Malpighi Hosp, Dept Expt Diagnost & Specialty Med, Haematopathol Unit, I-40138 Bologna, Italy
[6] Spanish Natl Canc Res Inst CNIO, Monodonal Antibodies Unit, Madrid 28029, Spain
关键词
TOX; mycosis fungoides; Sezary syndrome; T-CELL LYMPHOMA; ENDOTHELIAL GROWTH-FACTOR; MOBILITY GROUP BOX; DENDRITIC CELLS; GENE-EXPRESSION; STAGE; PATTERNS; MARKERS; SKIN;
D O I
10.3390/diagnostics12071582
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mycosis 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 x), 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.
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页数:11
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