» Articles » PMID: 9736018

Trisomy 3 is Not a Common Feature in Malignant Lymphomas of Mucosa-associated Lymphoid Tissue Type

Overview
Journal Am J Pathol
Publisher Elsevier
Specialty Pathology
Date 1998 Sep 15
PMID 9736018
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

The genetic background of extranodal marginal zone B-cell non-Hodgkin's lymphoma (NHL) of mucosa-associated lymphoid tissue (MALT) type is poorly understood. In contrast to most entities of primary nodal lymphomas, few cytogenetic data are available, and gene rearrangements frequently encountered in and highly characteristic of certain entities of systemic NHL are absent in this type of lymphoma. Recently, it was suggested that MALT-type NHLs are associated with certain numerical chromosome aberrations and especially with trisomy 3. We performed an extensive study using a sensitive double (bicolor) fluorescence in situ hybridization technique for the analysis of trisomies for chromosomes 3, 7, 12, and 18 in 60 samples of low-grade and 45 high-grade MALT-type tumors. In the low-grade cases, trisomy 3 was found in a frequency of only 20%. High-grade lymphomas of MALT type were associated with trisomies 3, 7, 12, and 18 in 36, 20, 18, and 13% of the cases, respectively. Whereas no difference was encountered for trisomy 3 in primary and secondary/simultaneous high-grade lymphomas, +7 and +12 were associated with primary lymphomas, and a +18 was predominantly found in secondary/simultaneous high-grade NHL. These results challenge earlier reports describing a high frequency of +3 in low-grade MALT-type NHL and indicate a possibly different genetic evolution pattern of primary and secondary/simultaneous high-grade lymphomas of primary mucosal origin.

Citing Articles

Recent Advances in the Genetic of MALT Lymphomas.

Rodriguez-Sevilla J, Salar A Cancers (Basel). 2022; 14(1).

PMID: 35008340 PMC: 8750177. DOI: 10.3390/cancers14010176.


Epidemiological characterization, genetic alterations of Helicobacter pylori infection in chronic gastric disorder and prognostic values of heterozygosity loss in chromosome 3p.

Ali Abuderman A, Syed R, Mateen A, Malik A, Ola M Mol Biol Rep. 2019; 46(4):4323-4332.

PMID: 31250359 DOI: 10.1007/s11033-019-04886-5.


Management of gastric mucosa-associated lymphoid tissue lymphoma in patients with extra copies of the gene.

Iwamuro M, Takenaka R, Nakagawa M, Moritou Y, Saito S, Hori S World J Gastroenterol. 2017; 23(33):6155-6163.

PMID: 28970731 PMC: 5597507. DOI: 10.3748/wjg.v23.i33.6155.


Molecular Aspects of H. pylori-Related MALT Lymphoma.

Owens S, Smith L Patholog Res Int. 2011; 2011:193149.

PMID: 21318155 PMC: 3034981. DOI: 10.4061/2011/193149.


Fluorescence in situ hybridization (FISH) analysis of primary ocular adnexal MALT lymphoma.

Tanimoto K, Sekiguchi N, Yokota Y, Kaneko A, Watanabe T, Maeshima A BMC Cancer. 2006; 6:249.

PMID: 17052360 PMC: 1630703. DOI: 10.1186/1471-2407-6-249.


References
1.
Kerrigan D, Irons J, Chen I . bcl-2 gene rearrangement in salivary gland lymphoma. Am J Surg Pathol. 1990; 14(12):1133-8. DOI: 10.1097/00000478-199012000-00005. View

2.
Barth T, Dohner H, WERNER C, Stilgenbauer S, Schlotter M, Pawlita M . Characteristic pattern of chromosomal gains and losses in primary large B-cell lymphomas of the gastrointestinal tract. Blood. 1998; 91(11):4321-30. View

3.
Haaf T, Schmid M . Chromosome topology in mammalian interphase nuclei. Exp Cell Res. 1991; 192(2):325-32. DOI: 10.1016/0014-4827(91)90048-y. View

4.
Hopman A, van Hooren E, Van De Kaa C, Vooijs P, Ramaekers F . Detection of numerical chromosome aberrations using in situ hybridization in paraffin sections of routinely processed bladder cancers. Mod Pathol. 1991; 4(4):503-13. View

5.
Wotherspoon A, Pan L, Diss T, Isaacson P . Cytogenetic study of B-cell lymphoma of mucosa-associated lymphoid tissue. Cancer Genet Cytogenet. 1992; 58(1):35-8. DOI: 10.1016/0165-4608(92)90130-z. View