دورية أكاديمية

Patterns of genomic aberrations suggest that Burkitt lymphomas with complex karyotype are distinct from other aggressive B-cell lymphomas with MYC rearrangement

التفاصيل البيبلوغرافية
العنوان: Patterns of genomic aberrations suggest that Burkitt lymphomas with complex karyotype are distinct from other aggressive B-cell lymphomas with MYC rearrangement
المؤلفون: Havelange, Violaine, Ameye, Geneviève, Théate, Ivan, Callet-Bauchu, Evelyne, Mugneret, Francine, Michaux, Lucienne, Dastugue, Nicole, Penther, Dominique, Barin, Carole, Collonge-Rame, Marie-Agnès, Baranger, Laurence, Terré, Christine, Nadal, Nathalie, Lippert, Eric, Laï, Jean-Luc, Cabrol, Christine, Tigaud, Isabelle, Herens, Christian, Hagemeijer, Anne, Raphael, Martine, Libouton, Jeanne-Marie, Poirel, Hélène, GFCH (Groupe Francophone de Cytogénétique Hématologique)
المساهمون: UCL - SSS/DDUV - Institut de Duve, UCL - SSS/IREC - Institut de recherche expérimentale et clinique, UCL - (SLuc) Service d'hématologie, UCL - (SLuc) Service d'anatomie pathologique, UCL - (SLuc) Centre de génétique médicale UCL
المصدر: Genes, Chromosomes & Cancer, Vol. 52, no.1, p. 81-92 (2013)
بيانات النشر: JohnWiley & Sons, Inc.
سنة النشر: 2013
المجموعة: DIAL@UCL (Université catholique de Louvain)
مصطلحات موضوعية: Abnormal Karyotype, Genes, myc, Humans, In Situ Hybridization, Fluorescence, Lymphoma, B-Cell, Male, Adolescent, Burkitt Lymphoma, Child, Preschool, Chromosome Aberrations, Chromosomes, Human, Female, Gene Rearrangement
الوصف: We previously showed that complex karyotypes (CK) and chromosome 13q abnormalities have an adverse prognostic impact in childhood Burkitt lymphomas/leukemias (BL) and diffuse large B-cell lymphomas (DLBCL). The aim of our study was to identify recurrent alterations associated with MYC rearrangements in aggressive B-cell lymphomas with CK. Multicolor fluorescence in situ hybridization (M-FISH) was performed in 84 patient samples (59 adults and 25 children), including 37 BL (13 lymphomas and 24 acute leukemias), 12 DLBCL, 28 B-cell lymphomas with intermediate features (DLBCL/BL), 4 B-cell precursor acute lymphoblastic leukemias (BCP-ALL), and 3 unclassifiable B-cell lymphomas. New (cytogenetically undetected) abnormalities were identified in 80% of patients. We also refined one-third of the chromosomal aberrations detected by karyotyping. M-FISH proved to be more useful in identifying chromosomal partners involved in unbalanced translocations and in revealing greater complexity of 13q rearrangements. Most of the newly identified or refined recurrent alterations involved 1q, 13q and 3q (gains/losses), 7q and 18q (gains), or 6q (losses), suggesting that these secondary aberrations may play a role in lymphomagenesis. Several patterns of genomic aberrations were identified: 1q gains in BL, trisomies 7 in DLBCL, and 18q-translocations in adult non-BL. BCP-ALL usually displayed an 18q21 rearrangement. BL karyotypes were less complex and aneuploid than those of other MYC-rearranged lymphomas. BCP-ALL and DLBCL/BL were associated with a higher rate of early death than BL and DLBCL. These findings support the categorization of DLBCL/BL as a distinct entity and suggest that BL with CK are indeed different from other aggressive MYC-rearranged lymphomas, which usually show greater genetic complexity. © 2012 Wiley Periodicals, Inc.
نوع الوثيقة: article in journal/newspaper
اللغة: Ndonga
تدمد: 1045-2257
1098-2264
العلاقة: boreal:156753; http://hdl.handle.net/2078.1/156753Test; info:pmid/23012230; urn:ISSN:1045-2257; urn:EISSN:1098-2264
DOI: 10.1002/gcc.22008
الإتاحة: https://doi.org/10.1002/gcc.22008Test
http://hdl.handle.net/2078.1/156753Test
حقوق: info:eu-repo/semantics/restrictedAccess
رقم الانضمام: edsbas.415EF57B
قاعدة البيانات: BASE
الوصف
تدمد:10452257
10982264
DOI:10.1002/gcc.22008