Plasma cell and terminal B-cell differentiation in mantle cell lymphoma mainly occur in the SOX11-negative subtype.
Autor: | Ribera-Cortada I; Hematopathology Unit, Department of Anatomic Pathology, Hospital Clinic, University of Barcelona, Barcelona, Spain.; Hospital Nostra Senyora de Meritxell, Escaldes-Engordany, Principat d'Andorra., Martinez D; Hematopathology Unit, Department of Anatomic Pathology, Hospital Clinic, University of Barcelona, Barcelona, Spain., Amador V; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain., Royo C; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain., Navarro A; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain., Beà S; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain., Gine E; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.; Department of Hematology, Hospital Clinic, University of Barcelona, Barcelona, Spain., de Leval L; Institute of Pathology, Centre Hospitalier Universitaire Vaudois, Lausanne, Switzerland., Serrano S; Department of Pathology, Hospital del Mar, Autonomous University of Barcelona, Barcelona, Spain., Wotherspoon A; Department of Histopathology, Royal Marsden Hospital, London, UK., Colomer D; Hematopathology Unit, Department of Anatomic Pathology, Hospital Clinic, University of Barcelona, Barcelona, Spain.; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain., Martinez A; Hematopathology Unit, Department of Anatomic Pathology, Hospital Clinic, University of Barcelona, Barcelona, Spain.; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain., Campo E; Hematopathology Unit, Department of Anatomic Pathology, Hospital Clinic, University of Barcelona, Barcelona, Spain.; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain. |
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Jazyk: | angličtina |
Zdroj: | Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc [Mod Pathol] 2015 Nov; Vol. 28 (11), pp. 1435-47. Date of Electronic Publication: 2015 Sep 11. |
DOI: | 10.1038/modpathol.2015.99 |
Abstrakt: | Mantle cell lymphoma is a mature lymphoid neoplasm characterized by the t(11;14)(q13;q32) and cyclin D1 overexpression. SOX11 is a transcription factor commonly overexpressed in these tumors but absent in most other mature B-cell lymphomas whose function is not well understood. Experimental studies have shown that silencing of SOX11 in mantle cell lymphoma cells promotes the shift from a mature B cell into an early plasmacytic differentiation phenotype, suggesting that SOX11 may contribute to tumor development by blocking the B-cell differentiation program. The relationship between SOX11 expression and terminal B-cell differentiation in primary mantle cell lymphoma and its relationship to the plasmacytic differentiation observed in occasional cases is not known. In this study we have investigated the terminal B-cell differentiation phenotype in 60 mantle cell lymphomas, 41 SOX11-positive and 19 SOX11-negative. Monotypic plasma cells and lymphoid cells with plasmacytic differentiation expressing cyclin D1 were observed in 7 (37%) SOX11-negative but in none of 41 SOX11-positive mantle cell lymphomas (P<0.001). Intense cytoplasmic expression of a restricted immunoglobulin light chain was significantly more frequent in SOX11-negative than -positive tumors (58 vs 13%) (P=0.001). Similarly, BLIMP1 and XBP1 expression was also significantly more frequent in SOX11-negative than in -positive cases (83 vs 34% and 75 vs 11%, respectively) (P=0.001). However, no differences in the expression of IRF4/MUM1 were observed among these subtypes of mantle cell lymphoma. In conclusion, these results indicate that SOX11-negative mantle cell lymphoma may be a particular subtype of this tumor characterized by more frequent morphological and immunophenotypic terminal B-cell differentiation features that may be facilitated by the absence of SOX11 transcription factor. |
Databáze: | MEDLINE |
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