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Characterization of 6q deletions in mature B cell lymphomas and childhood acute lymphoblastic leukemia
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2008 (English)In: Leukemia and Lymphoma, ISSN 1042-8194, E-ISSN 1029-2403, Vol. 49, no 3, 477-487 p.Article in journal (Refereed) Published
Abstract [en]

The study was undertaken with the aim to outline deletion patterns involving the long arm of chromosome 6, a common abnormality in lymphoproliferative disorders. Using a chromosome 6 specific tile path array, 60 samples from in total 49 cases with mantle cell lymphoma (MCL), de novo diffuse large B-cell lymphoma (DLBCL), transformed DLBCL as well as preceding follicular lymphoma (FL), and childhood acute lymphoblastic leukemia (ALL), were characterized. Twenty-six of the studied cases, representing all diagnoses, showed a 6q deletion among which 85% involved a 3Mb region in 6q21. The minimal deleted interval in 6q21 encompasses the FOXO3A, PRDM1 and HACE1 candidate genes. The PRDM1 gene was found homozygously deleted in a case of DLBCL. Moreover, in two DLBCL cases, an overlapping homozygous deletion was identified in 6q23.3-24.1, encompassing the TNFAIP3 gene among others. Taken together, we refined the deletion pattern within the long arm of chromosome 6 in four different types of hematological malignances, suggesting the location of tumor suppressor genes involved in the tumor progression.

Place, publisher, year, edition, pages
2008. Vol. 49, no 3, 477-487 p.
Keyword [en]
6q, deletion, MCL, DLBCL, FL, ALL
National Category
Medical and Health Sciences
Identifiers
URN: urn:nbn:se:uu:diva-16378DOI: 10.1080/10428190701817282ISI: 000253513300015PubMedID: 18297524OAI: oai:DiVA.org:uu-16378DiVA: diva2:44149
Available from: 2008-05-20 Created: 2008-05-20 Last updated: 2017-12-08Bibliographically approved

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Berglund, MattiasRosenquist, Richard

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Department of Oncology, Radiology and Clinical ImmunologyDepartment of Genetics and Pathology
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