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PMID: 15682443 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

MALT lymphoma with t(14;18)(q32;q21)/IGH-MALT1 is characterized by strong cytoplasmic MALT1 and BCL10 expression.

The Journal of pathology ·Vol. 205 ·No. 3 ·2005-02-00 ·Pages 293-301

Ye H, Gong L, Liu H, Hamoudi RA, Shirali S, Ho L, Chott A, Streubel B, Siebert R, Gesk S, Martin-Subero JI, Radford JA, Banerjee S, Nicholson AG, Ranaldi R, Remstein ED, Gao Z, Zheng J, Isaacson PG, Dogan A, Du MQ

Abstract

Mucosa-associated lymphoid tissue (MALT) lymphoma is specifically associated with t(11;18)(q21;q21), t(1;14)(p22;q32) and t(14;18)(q32;q21). t(11;18)(q21;q21) fuses the N-terminus of the API2 gene to the C-terminus of the MALT1 gene and generates a functional API2-MALT1 product. t(1;14)(p22;q32) and t(14;18)(q32;q21) bring the BCL10 and MALT1 genes respectively to the IGH locus and deregulate their expression. The oncogenic activity of the three chromosomal translocations is linked by the physiological role of BCL10 and MALT1 in antigen receptor-mediated NFkappaB activation. In this study, MALT1 and BCL10 expression was examined in normal lymphoid tissues and 423 cases of MALT lymphoma from eight sites, and their expression was correlated with the above translocations, which were detected by molecular and molecular cytogenetic methods. In normal B-cell follicles, both MALT1 and BCL10 were expressed predominantly in the cytoplasm, high in centroblasts, moderate in centrocytes and weak/negative in mantle zone B-cells. In MALT lymphoma, MALT1 and BCL10 expression varied among cases with different chromosomal translocations. In 9/9 MALT lymphomas with t(14;18)(q32;q21), tumour cells showed strong homogeneous cytoplasmic expression of both MALT1 and BCL10. In 12/12 cases with evidence of t(1;14)(p22;q32) or variants, tumour cells expressed MALT1 weakly in the cytoplasm but BCL10 strongly in the nuclei. In all 67 MALT lymphomas with t(11;18)(q21;q21), tumour cells expressed weak cytoplasmic MALT1 and moderate nuclear BCL10. In MALT lymphomas without the above translocations, both MALT1 and BCL10, in general, were expressed weakly in the cytoplasm. Real-time quantitative RT-PCR showed a good correlation between MALT1 and BCL10 mRNA expression and underlining genetic changes, with t(14;18)(q32;q21)- and t(1;14)(p22;q32)-positive cases displaying the highest MALT1 and BCL10 mRNA expression respectively. These results show that MALT1 expression pattern is identical to that of BCL10 in normal lymphoid tissues but varies in MALT lymphomas, with high cytoplasmic expression of both MALT1 and BCL10 characterizing those with t(14;18)(q32;q21).

MeSH Terms
Adaptor Proteins, Signal Transducing/genetics,metabolism B-Cell CLL-Lymphoma 10 Protein Caspases Chromosomes, Human, Pair 14/genetics Chromosomes, Human, Pair 18/genetics Cytoplasm/metabolism Female Gene Expression Humans Lymphoid Tissue/metabolism Lymphoma, B-Cell, Marginal Zone/genetics,metabolism Male Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein Neoplasm Proteins/genetics,metabolism RNA, Messenger/genetics RNA, Neoplasm/genetics Reverse Transcriptase Polymerase Chain Reaction/methods Translocation, Genetic
Chemicals
Adaptor Proteins, Signal Transducing B-Cell CLL-Lymphoma 10 Protein BCL10 protein, human Neoplasm Proteins RNA, Messenger RNA, Neoplasm Caspases MALT1 protein, human Mucosa-Associated Lymphoid Tissue Lymphoma Translocation 1 Protein
Authors & Affiliations
21 authors, click to expand affiliations / ORCID
Ye Hongtao
Department of Pathology, University of Cambridge, Cambridge, UK.
Gong Liping
Liu Hongxiang
Hamoudi Rifat A
Shirali Sima
Ho Liza
Chott Andreas
Streubel Berthold
Siebert Reiner
Gesk Stefan
Martin-Subero Jose I
Radford John A
Banerjee Sankar
Nicholson Andrew G
Ranaldi Renzo
Remstein Ellen D
Gao Zifen
Zheng Jie
Isaacson Peter G
Dogan Ahmet
Du Ming-Qing
Article Info
Journal
The Journal of pathology
Abbr.
J Pathol
ISSN
0022-3417
Published
2005-02-00
Pages
293-301
Language
English
Region
England
NLM ID
0204634
Subset
IM
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