Detection of clonal T-cell populations in gastrointestinal lymphomas by analysis of cRNA conformational polymorphisms of rearranged T-cell-receptor-gamma genes

Br J Haematol. 1994 Feb;86(2):316-21. doi: 10.1111/j.1365-2141.1994.tb04732.x.

Abstract

Analysis of complementary RNA molecules of junctional regions of rearranged T-cell-receptor-gamma genes show a pattern of conformational polymorphisms which is specific for an individual lymphocytic clone. In a blinded study we analysed formalin-fixed, paraffin-embedded histological specimens from gastrointestinal lymphomas and control tissues (lymphomas: pleomorphic T-cell 10, anaplastic large cell [Ki1+] 9, centroblastic 5, immunocytoma 1, B-CLL 2, Hodgkin's 2, centroblastic-centrocytic 1, MALT [mucosa associated lymphoid tissue] 1, T-cell acute lymphoblastic leukaemia 1, non-lymphoid or polyclonal lymphoid tissues 5). Junctional regions of rearranged TCR-gamma genes were amplified by the polymerase chain reaction and the products were transcribed into cRNA. Conformational patterns of cRNA molecules were analysed by polyacrylamide gel electrophoresis. 13/20 T-lineage lymphomas and the T-cell acute lymphocytic leukaemia displayed a distinct cRNA band pattern, all B-lineage lymphomas and the non-lymphoid control tissues were negative. Only one case of nasopharyngeal (lymphoepithelial, Schmincke-Regaud) carcinoma showed a faint cRNA banding pattern. This novel and non-radioactive assay allows for the rapid detection and molecular characterization of clonal lymphoid populations in minute histological biopsy specimens.

MeSH terms

  • Base Sequence
  • Electrophoresis, Polyacrylamide Gel
  • Gene Rearrangement, gamma-Chain T-Cell Antigen Receptor*
  • Humans
  • Lymphoma, Non-Hodgkin / genetics*
  • Molecular Sequence Data
  • Neoplastic Stem Cells / pathology
  • Polymerase Chain Reaction
  • RNA, Complementary / analysis*
  • RNA, Neoplasm / analysis
  • Stomach Neoplasms / genetics*
  • T-Lymphocytes / pathology*

Substances

  • RNA, Complementary
  • RNA, Neoplasm