Trisomy 3 in marginal zone B-cell lymphoma: A study based on cytogenetic analysis and fluorescence in situ hybridization

Dierlamm, J.;Michaux, Lucienne;Wlodarska, Iwona;Pittaluga, S.;Vandenberghe, Hans;et.al.
(1996) British Journal of Haematology — Vol. 93, n° 1, p. 242-249 (1996)

Files

No attached file found for this publication.

Details

Authors
  • Dierlamm, J.
    Author
  • Michaux, LucienneUCLouvain
    Author
  • Wlodarska, IwonaUCLouvain
    Author
  • Pittaluga, S.
    Author
  • Vandenberghe, Hans
    Author
Show more
Abstract
Trisomy 3 represents the most frequent and consistent chromosomal abnormality characterizing the recently defined entity marginal zone B-cell lymphoma (MZBCL). By cytogenetic analysis and/or fluorescence in situ hybridization (FISH) on interphase nuclei we found an increased copy number of chromosome 3 in 22/36 (61%) successfully analysed cases, including 8/12 cases with extranodal MZBCL, 8/13 cases with nodal MZBCL, and 6/11 patients with splenic MZBCL. Sensitivity of interphase cytogenetics was somewhat higher than that of conventional cytogenetic investigation, Structural chromosomal changes involving at least one chromosome 3 were seen in 11/20 cases with an increased copy number of chromosome 3: +del(3)(p13) was demonstrated in three cases, and was the sole chromosomal abnormality in one of them: +i(3)(q10) was seen in two other patients; and rearrangements involving various breakpoints on the long arm of chromosome 3 were found in the remaining cases, FISH on metaphase spreads confirmed these structural abnormalities and additionally showed two unexpected translocations involving chromosome 3, We conclude that: (1) trisomy 3 occurs in a high proportion of extranodal, nodal and splenic MZBCL; (2) FISH on interphase nuclei is an additional and sensitive tool in detecting an increased copy number of chromosome 3 in MZBCL; (3) additional structural abnormalities involving the long arm of chromosome 3 are frequent but non-recurrent and are perhaps secondary changes; and (4) abnormalities such as +del(3)(p13) and +i(3)(q10) suggest that genes located on the long arm of chromosome 3 are of particular importance in the pathogenesis of MZBCL.
Affiliations

Citations

Dierlamm, J., Michaux, L., Wlodarska, I., Pittaluga, S., Zeller, W., Stul, M., Criel, A., Thomas, J., Boogaerts, M., Delaère, P., Cassiman, JJ., Dewolfpeeters, C., Mecucci, C., & Vandenberghe, H. (1996). Trisomy 3 in marginal zone B-cell lymphoma: A study based on cytogenetic analysis and fluorescence in situ hybridization. British Journal of Haematology, 93(1), 242-249. https://doi.org/10.1046/j.1365-2141.1996.522522.x (Original work published 1996)