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Transcript
Atlas of Genetics and Cytogenetics
in Oncology and Haematology
OPEN ACCESS JOURNAL AT INIST-CNRS
Leukaemia Section
Mini Review
Mantle cell lymphoma
Jean-Loup Huret
Genetics, Dept Medical Information, University of Poitiers, CHU Poitiers Hospital, F-86021 Poitiers, France
Published in Atlas Database: May 1998
Online updated version: http://AtlasGeneticsOncology.org/Anomalies/mantle2062.html
DOI: 10.4267/2042/37456
This work is licensed under a Creative Commons Attribution-Non-commercial-No Derivative Works 2.0 France Licence.
© 1998 Atlas of Genetics and Cytogenetics in Oncology and Haematology
generalized lymphadenopathies in 90%, bone marrow
involvement (70%), frequent splenomegaly (50%),
hepatomegaly (30%), and gastro-intestinal involvement
(20%), and lymphocytosis (30%); elevated LDH in
50%.
Pathology
Small cleaved cell B-lymphocytes with inconspicuous
nucleoli and pale cytoplasm; with a pan B-cell, CD5+,
CD10-, CD23- (in contrast with CLL) phenotype;
diffuse, nodular and blastoid types, the latter having
large cells and higher mitotic count.
Clinics and pathology
Disease
NHL of the low to intermediate grade.
Phenotype / cell stem origin
B-cell lineage.
Epidemiology
5% of NHL; sex ratio: 3M/1F; median age: 65 yrs.
Clinics
Advanced disease (Ann Harbor stage III-IV) with
Leukemic phase of mantle cell lymphoma. Peripheral blood. Small to medium sized lymphoid cells with slightly to markedly irregular
nuclear contour. The nuclei have moderately dispersed chromatin bur inconspicuous nucleoli. From a patient with
46,XX,t(11;14)(q13;q32) - Courtesy Georges Flandrin.
Atlas Genet Cytogenet Oncol Haematol. 1998;2(4)
127
Mantle cell lymphoma
Huret JL
(junctions genes of IgH) and C in 3'; the breakpoint in
BCL1 is in MTC (major translocation cluster),
centromeric to the gene (in 5'), in 80% of cases, or
dispersed in mTC1, 2, or 3 in 5' of the gene or in the 3'
untranslated region of exon 5.
Treatment
According to the age and the disease stage.
Prognosis
Median survival is 3 to 4 yrs; less than 2 yrs in the case
of a leukaemic form (blastoid); in contrast with the
good prognosis of the MALT lymphoma, a closely
related disease.
Fusion protein
Description
No fusion protein, but promoter exchange; the
immunoglobulin gene enhancer stimulates the
expression of BCL1.
Oncogenesis
Overexpression of BCL1 accelerates passage through
the G1 phase.
Cytogenetics
Cytogenetics, morphological
Knowledge is still scarce, and data complex.
t(11;14)(q13;q32) is found in 50-70% of cases, but this
translocation may also, at a much lesser frequency, be
found in other diseases; the genes involved in this
translocation are described below; t(11;14) is found in
complex karyotypes.
Other frequent findings: deletion of parts of: 1p, 6q, 9p,
11q (in particular 11q22-23), 13q; gains of parts of: 3q,
8q, 15q; frequent markers; tetraploidy may be found,
especially in the blastoid subtype.
References
Rimokh R, Berger F, Delsol G, Charrin C, Bertheas MF,
Ffrench M, Garoscio M, Felman P, Coiffier B, Bryon PA, et al.
Rearrangement and overexpression of the BCL-1/PRAD-1
gene in intermediatelymphocytic lymphomas and in t(11q13)bearing leukemias. Blood 1993 Jun 1;81(11):3063-7.
Maloney DG. Non-Hodgkin's lymphoma. Curr Opin Hematol
1995 Jul;2(4):255-61. (Review).
Cytogenetics, molecular
CGH (compatrative genomic hybridization) may
disclose important events in this disease, taken into
account that the t(11;14) may be insufficient for
oncogenesis; furthermore, this and other molecular
cytogenetic techniques may come in addition to the
usual techniques to 'dissect' complex karyotypes.
Argatoff LH, Connors JM, Klasa RJ, Horsman DE, Gascoyne.
Mantle cell lymphoma: a clinicopathologic study of 80 cases.
Blood 1997 Mar 15;89(6):2067-78.
Donner LR. Cytogenetics of lymphomas: a brief review of its
theoretical and practical significance. Cancer Genet Cytogenet
1997 Mar;94(1):20-6.
Meusers P, Hense J, Brittinger G. Mantle cell lymphoma:
diagnostic criteria, clinical aspects and therapeutic problems.
Leukemia 1997 Apr;11 Suppl 2:S60-4. (Review).
Genes involved and Proteins
Ott G, Kalla J, Ott MM, Schryen B, Katzenberger T, Muller JG,
Muller-Hermelink HK. Blastoid variants of mantle cell
lymphoma: frequent bcl-1 rearrangements at the major
translocation cluster region and tetraploid chromosome clones.
Blood 1997 Feb 15;89(4):1421-9.
BCL1
Location: 11q13
DNA / RNA
5 exons.
Protein
Encodes the cyclin D1; role in the cell cycle control:
G1 progression and G1/S transition.
Bosch F, Lopez-Guillermo A, Campo E, Ribera JM, Conde E,
Piris MA, Vallespi T, Woessner S, Montserrat E. Mantle cell
lymphoma: presenting features, response to therapy, and
prognostic factors. Cancer 1998 Feb 1;82(3):567-75.
Monni O, Oinonen R, Elonen E, Franssila K, Teerenhovi L,
Joensuu H, Knuutila S. Gain of 3q and deletion of 11q22 are
frequent aberrations in mantle cell lymphoma. Genes
Chromosomes Cancer 1998 Apr;21(4):298-307.
IgH
Location: 14q32
This article should be referenced as such:
Results of the chromosomal
anomaly
Huret JL. Mantle cell lymphoma. Atlas Genet Cytogenet Oncol
Haematol.1998;2(4):127-128.
Hybrid gene
Description
5' BCL1 translocated on chromosome 14 near JH
Atlas Genet Cytogenet Oncol Haematol. 1998;2(4)
128
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