| Title | Expression of the Brain Transcription Factor OTX1 Occurs in a Subset of Normal Germinal-Center B Cells and in Aggressive Non-Hodgkin Lymphoma. | | Author(s) | Omodei D, Acampora D, Russo F, De Filippi R, Severino V, Di Francia R, Frigeri F, Mancuso P, De Chiara A, Pinto A, Casola S, Simeone A | | Institution | From the Centro di Ingegneria (CEINGE) Biotecnologie Avanzate,* Naples, Italy; Institute of Genetics and Biophysics "A. Buzzati-Traverso", Naples, Italy; Hematology-Oncology Unit and Stem Cells Transplantation, and Pathology Unit, Instituto Nationale Tumori, Fondazione 'G. Pascale', Instituto di Ricovero e Cura a Carattere Scientifico (IRCSS), Naples, Italy; Department of Cellular and Molecular Biology and Pathology, University of Naples 'Federico II', Naples, Italy; Pathology Unit, Istituto FIRC (Fondazione Italiana per la Ricerca sul Cancro) di Oncologia Molecolare (IFOM), IFOM-IEO (Instituto Europeo Oncologico) Campus, Milan, Italy; and Scuola Europea di Medicina Molecolare (SEMM),** Naples, Italy. | | Source | Am J Pathol 2009 Nov 5. | | Abstract | The roles in brain development. Previous studies have shown the association between OTX2 and OTX1 with anaplastic and desmoplastic medulloblastomas, respectively. Here, we investigated OTX1 and OTX2 expression in Non-Hodgkin Lymphoma (NHL) and multiple myeloma. A combination of semiquantitative RT-PCR, Western blot, and immunohistochemical analyses was used to measure OTX1 and OTX2 levels in normal lymphoid tissues and in 184 tumor specimens representative of various forms of NHL and multiple myeloma. OTX1 expression was activated in 94% of diffuse large B-cell lymphomas, in all Burkitt lymphomas, and in 90% of high-grade follicular lymphomas. OTX1 was undetectable in precursor-B lymphoblastic lymphoma, chronic lymphocytic leukemia, and in most marginal zone and mantle cell lymphomas and multiple myeloma. OTX2 was undetectable in all analyzed malignancies. Analysis of OTX1 expression in normal lymphoid tissues identified a subset of resting germinal center (GC) B cells lacking PAX5 and BCL6 and expressing cytoplasmic IgG and syndecan. About 50% of OTX1(+) GC B cells co-expressed CD10 and CD20. This study identifies OTX1 as a molecular marker for high-grade GC-derived NHL and suggests an involvement of this transcription factor in B-cell lymphomagenesis. Furthermore, OTX1 expression in a subset of normal GC B cells carrying plasma cell markers suggests its possible contribution to terminal B-cell differentiation. | | Language | ENG | | Pub Type(s) | JOURNAL ARTICLE
| | PubMed ID | 19893048 |
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