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Molecular heterogeneity of B‐lineage diffuse large cell lymphoma
Author(s) -
Volpe Gisella,
Vitolo Umberto,
Carbone Antonino,
Pastore Cristina,
Bertini Marilena,
Botto Barbara,
Audisio Ernesta,
Freilone Roberto,
Novero Domenico,
Cappia Susanna,
De Giuli Paolo,
Mazza Umberto,
Resegotti Luigi,
Palestro Giorgio,
Saglio Giuseppe,
Gaidano Gianluca
Publication year - 1996
Publication title -
genes, chromosomes and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.754
H-Index - 119
eISSN - 1098-2264
pISSN - 1045-2257
DOI - 10.1002/(sici)1098-2264(199605)16:1<21::aid-gcc3>3.0.co;2-5
Subject(s) - bcl6 , lineage (genetic) , biology , lymphoma , genetic heterogeneity , mutation , cancer research , pathogenesis , genetics , gene , phenotype , b cell , immunology , germinal center , antibody
B‐lineage diffuse large cell lymphoma (B‐DLCL) arising de novo is characterized by a marked degree of clinical heterogeneity. To determine whether or not the clinical heterogeneity of de novo B‐DLCL is reflected by heterogeneity in the molecular features of these tumors, we investigated the pattern of distribution of several genetic lesions in 70 cases of de novo B‐DLCL at diagnosis. The panel of genetic lesions tested comprised the molecular alterations most frequently detected in B‐DLCL, including rearrangements of BCL2, BCL6, and MYC as well as deletions of 6q and mutations of TP53. One or more genetic lesions were detected in 39/70 cases of B‐DLCL. Isolated structural alterations of BCL2, BCL6, 6q or TP53 were detected in 8/70, 10/70, 11/70, and 3/70 cases, respectively. No isolated MYC lesions were detected. Six cases carried different combinations of two genetic lesions, including lesions of BCL2 + BCL6 (1 case), BCL2 + MYC (1 case), BCL2 + 6q (2 cases), or BCL6 + 6q (2 cases). One case had accumulated three genetic lesions, namely a rearrangement of BCL2 and BCL6 and a mutation of TP53. Overall, these data show that multiple distinct patterns of genetic lesions may associate with de novo B‐DLCL, indicating that the molecular pathogenesis of this group of lymphomas is characterized by a high degree of molecular heterogeneity. Genes Chromosom Cancer 16:21–30 (1996). © 1996 Wiley‐Liss, Inc.