t(9;14)(p13;q32)/PAX5-IGH translocation as a secondary cytogenetic abnormality in diffuse large B-cell lymphoma
Author:
Affiliation:
1. Tenri Institute of Medical Research, Tenri Hospital, Nara, Japan,
2. Department of Hematology, Tenri Hospital, Nara, Japan,
3. Department of Diagnostic Pathology, Tenri Hospital, Nara, Japan
Publisher
Japanese Society for Lymphoreticular Tissue Research
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/jslrt/61/4/61_21025/_pdf
Reference19 articles.
1. 1 Offit K, Parsa NZ, Filippa D, Jhanwar SC, Chaganti RS. t(9;14)(p13;q32) denotes a subset of low-grade non-Hodgkin’s lymphoma with plasmacytoid differentiation. Blood. 1992; 80: 2594-2599.
2. 2 Iida S, Rao PH, Nallasivam P et al. The t(9;14)(p13;q32) chromosomal translocation associated with lymphoplasmacytoid lymphoma involves the PAX-5 gene. Blood. 1996; 88: 4110-4117.
3. 3 Morrison AM, Jäger U, Chott A et al. Deregulated PAX-5 transcription from a translocated IgH promoter in marginal zone lymphoma. Blood. 1998; 92: 3865-3878.
4. 4 Ohno H, Furukawa T, Fukuhara S et al. Molecular analysis of a chromosomal translocation, t(9;14)(p13;q32), in a diffuse large-cell lymphoma cell line expressing the Ki-1 antigen. Proc Natl Acad Sci USA. 1990; 87: 628-632.
5. 5 Poppe B, De Paepe P, Michaux L et al. PAX5/IGH rearrangement is a recurrent finding in a subset of aggressive B-NHL with complex chromosomal rearrangements. Genes Chromosomes Cancer. 2005; 44: 218-223.
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1. EBF1, PAX5, and MYC: regulation on B cell development and association with hematologic neoplasms;Frontiers in Immunology;2024-01-22
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