Best Practice & Research Clinical Haematology
Volume 20, Issue 4 , Pages 571-596, December 2007

Genetic events in the pathogenesis of multiple myeloma

  • P.L. Bergsagel, MD (Associate Professor and Consultant)

      Affiliations

    • Corresponding Author InformationCorresponding author. Tel.: +1 480 301 4704; Fax: +1 480 301 8387.
  • W.M. Kuehl, MD (Chief of the Molecular Pathogenesis of Myeloma Section, Genetics Branch)

Mayo Clinic Arizona, Scottsdale, AZ 85260, USA

National Cancer Institute, Bethesda, MD, USA

Mayo Clinic, 13400 E Shea Blvd, Scottsdale, AZ 85259, USA

National Cancer Institute, Bethesda, MD, USA

The genetics of myeloma has been increasingly elucidated in recent years. Recurrent genetic events, and also biologically distinct and clinically relevant genetic subtypes of myeloma have been defined. This has facilitated our understanding of the molecular pathogenesis of the disease. In addition, some genetic abnormalities have proved to be highly reproducible prognostic factors. With the expanding therapeutic armamentarium, it is time to include genetic assessment as part of clinical evaluation of myeloma patients to guide management. In this review we examine the role of various genetic abnormalities in the molecular pathogenesis of myeloma, and the use of such abnormalities in disease classification, prognosis and clinical management.

Key words: genetics, gene expression profiling, molecular pathogenesis, prognosis, IgH translocations, hyperdiploid

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PII: S1521-6926(07)00064-3

doi:10.1016/j.beha.2007.08.004

Best Practice & Research Clinical Haematology
Volume 20, Issue 4 , Pages 571-596, December 2007