Malignant Lymphomas |
1 Departments of Pathology
2 Medical Microbiology, Lund University Hospital
3 Department of Immunotechnology, CREATE Health, BioMedical Center (BMC) D13, Lund University, Lund, Sweden
Correspondence: Michael Dictor, Department of Pathology, Lund University Hospital, Sölvegatan 25, 22185 Lund, Sweden. E-mail:michael.dictor{at}med.lu.se
Background: We surveyed lymphomas to determine the range of expression of the mantle cell lymphoma-associated SOX11 transcription factor and its relation to cyclin D1.
Design and Methods: On hundred and seventy-two specimens were immunostained for the SOX11 N and C termini. Cyclin D1 was detected by immunohistochemistry and quantitative reverse transcriptase polymerase chain reaction; in situ hybridization for t(11;14) was applied when needed.
Results: Nuclear SOX11 was strongly expressed in most B and T-lymphoblastic leukemia/lymphomas and half of childhood Burkitts lymphomas, but only weakly expressed in some hairy cell leukemias. Chronic lymphocytic leukemia/lymphoma, marginal zone, follicular and diffuse large B-cell lymphomas were negative for SOX11, as were all cases of intermediate Burkitts lymphomas/diffuse large B-cell lymphoma, myeloma, Hodgkins lymphomas and mature T-cell and NK/T-cell lymphomas.
Conclusions: In addition to mantle cell lymphoma, SOX11 is strongly expressed only in lymphoblastic malignancies and Burkitts lymphomas. Its expression is independent of cyclin D1 (except for weak expression in hairy cell leukemias) and unlikely to be due to translocations in lymphoid neoplasia.
Key words: lymphoid, SOX11 transcription factors, lymphoblastic neoplasms, mantle cell lymphoma, Burkitts lymphoma.
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S. A. Pileri and B. Falini Mantle cell lymphoma Haematologica, November 1, 2009; 94(11): 1488 - 1492. [Full Text] [PDF] |
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