Analysis of the frequency of microsatellite instability and p53 gene mutation in splenic marginal zone and MALT lymphomas

被引:21
|
作者
Mateo, MS
Mollejo, M
Villuendas, R
Algara, P
Sánchez-Beato, M
Martinez-Delgado, B
Martínez, P
Piris, MA
机构
[1] Virgen Salud Hosp, Dept Pathol, Toledo 45004, Spain
[2] Virgen Salud Hosp, Dept Genet, Toledo 45004, Spain
[3] AV Reyes Catolicos, Fundac J Diaz, Dept Genet, Madrid 28040, Spain
来源
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY | 1998年 / 51卷 / 05期
关键词
splenic marginal zone lymphoma; mucosa associated lymphoid tissue lymphoma; p53; microsatellite instability;
D O I
10.1136/mp.51.5.262
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Aims-Studies of the genetic characteristics of splenic marginal zone lymphoma (SMZL) have failed to identify genetic changes specific to this tumour. Microsatellite instability is a type of genomic instability associated with different types of human cancer. Although microsatellite instability is rare in B cell non-Hodgkin's lymphomas, it has been found in some specific subsets, such as marginal zone lymphomas arising in mucosa associated lymphoid tissue (MALT),where an association with p53 mutation has been described. Because it has been proposed that SMZL and MALT are close in histogenetic terms, this study investigated the comparative frequency of microsatellite instability and p53 mutation in patients with SMZL and MALT lymphomas. Methods-Microsatellite instability was investigated using seven microsatellite marker loci in 14 patients with SMZL and 20 patients with MALT lymphomas. In an attempt to clarify the role of p53 gene mutation in the pathogenesis of SMZL, exons 5-8 were also investigated by polymerase chain reaction single strand conformation polymorphism (PCR-SSCP) and direct sequencing in a total of 20 patients with SMZL and 22 patients with MALT lymphomas. Results-Microsatellite instability was not detected in patients with SMZL, although five of 20 patients with MALT lymphomas had microsatellite instability. The frequency of p53 mutation was low in both series (two of 20 patients with SMZL and one of 22 patients with MALT lymphomas). No significant association was found between p53 mutation and microsatellite instability. Conclusions These results indicate that microsatellite instability is not associated with the molecular pathogenesis of SMZL, confirming the relatively increased frequency of microsatellite instability in MALT lymphomas, and perhaps suggesting that MALT and SMZL have different mechanisms of tumorigenesis.
引用
收藏
页码:262 / 267
页数:6
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