Cytogenetic analysis of a United Kingdom series of non-Hodgkins lymphomas

Cancer Genet Cytogenet. 1992 Jul 1;61(1):31-8. doi: 10.1016/0165-4608(92)90366-g.

Abstract

We describe cytogenetic analyses of cells derived from 40 non-Hodgkins lymphoma (NHL) node biopsies, 23 of which were from patients who had not been treated before biopsy. We noted that the chromosomes most frequently gained were X (32%), 12 (27%), and 3 (24%). Monosomies were much less common; loss of chromosome 13 (13.5%) was most frequent. Structural abnormalities primarily involved chromosomes 14 (70%), 1 (40.5%), 18 (38%), 6 (35%), and 17 (22%). Low-and high-grade disease showed similar patterns of structural changes; however, a markedly greater number of chromosome gains were associated with low-grade disease. Biopsy samples from patients who had previously been treated showed an increased frequency of structural abnormalities, as well as a significantly larger number of chromosome gains. The importance of these observations, particularly with regard to possible oncogene involvement in lymphoma evolution, is discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aneuploidy
  • Chromosome Aberrations*
  • Chromosomes, Human, Pair 14
  • Chromosomes, Human, Pair 17
  • Chromosomes, Human, Pair 18
  • Chromosomes, Human, Pair 6
  • Humans
  • Karyotyping
  • Lymph Nodes / ultrastructure
  • Lymphoma, Non-Hodgkin / genetics*