Higher rates of t(11;18) in Chinese patients with transformed type of MALT lymphoma suggest novel pathways for progression of the disease

Leuk Lymphoma. 2007 Nov;48(11):2157-66. doi: 10.1080/10428190701606818.

Abstract

To detect the t(11;18) chromosome translocation in different stages of mucosa-associated lymphoid tissue (MALT) lymphoma, we established a RT-PCR method by adopting three new primer pairs and using the RNA extracted from the paraffin tissues to amplify the t(11;18) fusion gene API2-MALT1 in shorter lengths. Our results showed five key findings, which are (a) higher detection rates of t(11;18) (21.13%) in Chinese patients with transformed MALT lymphoma, (b) lower detection rates of t(11;18) in stomach MALT lymphoma, (c) different organ localizations of MALT lymphoma in Chinese patients, (d) higher nuclear expression rates of Bcl-10 in low grade MALT (51.72%), and (e) lower response rates (50% CR, and 50% PR) to anti-H.-pylori therapy. These findings suggest novel pathways for low-grade MALT lymphoma to be progressed into transformed MALT lymphoma. This study also suggests that amplification of shorter length of PCR products from the paraffin-fixed tissues increases sensitivity, which is significant in improving the selection of the therapeutic regimen and assessing the prognosis of the disease.

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Algorithms
  • Anti-Bacterial Agents / therapeutic use
  • B-Cell CLL-Lymphoma 10 Protein
  • Base Sequence
  • Case-Control Studies
  • China
  • Chromosomes, Human, Pair 11*
  • Chromosomes, Human, Pair 18*
  • DNA Mutational Analysis
  • Disease Progression
  • Gene Expression Regulation, Neoplastic
  • Gene Frequency
  • Helicobacter Infections / complications
  • Helicobacter Infections / drug therapy
  • Humans
  • Lymphoma, B-Cell, Marginal Zone / complications
  • Lymphoma, B-Cell, Marginal Zone / genetics*
  • Molecular Sequence Data
  • Oncogene Proteins, Fusion / genetics
  • Signal Transduction / genetics*
  • Translocation, Genetic*

Substances

  • API2-MALT1 fusion protein, human
  • Adaptor Proteins, Signal Transducing
  • Anti-Bacterial Agents
  • B-Cell CLL-Lymphoma 10 Protein
  • BCL10 protein, human
  • Oncogene Proteins, Fusion