Immunoglobulin gene rearrangements and the pathogenesis of multiple myeloma.

D. González, M. van der Burg, R. García-Sanz, J.A. Fenton, A.W. Langerak, M. González, J.J. van Dongen, J.F. San Miguel, G.J. Morgan

Research output: Contribution to journalArticlepeer-review

166 Citations (Scopus)

Abstract

The ability to rearrange the germ-line DNA to generate antibody diversity is an essential prerequisite for the production of a functional repertoire. While this is essential to prevent infections, it also represents the "Achilles heel" of the B-cell lineage, occasionally leading to malignant transformation of these cells by translocation of protooncogenes into the immunoglobulin (Ig) loci. However, in evolutionary terms this is a small price to pay for a functional immune system. The study of the configuration and rearrangements of the Ig gene loci has contributed extensively to our understanding of the natural history of development of myeloma. In addition to this, the analysis of Ig gene rearrangements in B-cell neoplasms provides information about the clonal origin of the disease, prognosis, as well as providing a clinical useful tool for clonality detection and minimal residual disease monitoring. Herein, we review the data currently available on both Ig gene rearrangements and protein patterns seen in myeloma with the aim of illustrating how this knowledge has contributed to our understanding of the pathobiology of myeloma.
Original languageEnglish
Pages (from-to)3112-3121
Number of pages10
JournalBlood
Volume110
Issue number9
DOIs
Publication statusPublished - 01 Nov 2007

Keywords

  • Animals
  • Gene Expression Regulation
  • Gene Rearrangement
  • Gene Rearrangement, B-Lymphocyte, Heavy Chain
  • Gene Rearrangement, B-Lymphocyte, Light Chain
  • Genes, Immunoglobulin
  • Humans
  • Immunoglobulins
  • Models, Biological
  • Multiple Myeloma
  • Paraproteins
  • Recombination, Genetic
  • Somatic Hypermutation, Immunoglobulin
  • Translocation, Genetic

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