Journal of Clinical Oncology, Vol 23, No 26 (September 10), 2005: pp. 6379-6386
© 2005 American Society of Clinical Oncology.
DOI: 10.1200/JCO.2005.55.013
Molecular Pathogenesis of Hodgkin's Lymphoma
Daniel Re,
Ralf Küppers,
Volker Diehl
From the Department I of Internal Medicine, University of Cologne, Cologne; Institute for Cell Biology (Tumor Research), University of Duisburg-Essen Medical School, Essen, Germany; and the Burnham Institute, La Jolla, CA
Address reprint requests to Daniel Re, MD, The Burnham Institute, John Reed Laboratory, 10901 N. Torrey Pines Rd., La Jolla, CA 92037; e-mail: dre{at}burnham.org.
According to the WHO classification, Hodgkin's lymphoma (HL) is subdivided into a classical variant and a nodular lymphocyte predominant variant which are characterized by the presence of Hodgkin's and Reed-Sternberg (H-RS) cells or lymphocytic and histiocytic (L&H) cells, respectively. This article reviews genetic characteristics and transcriptional changes of H-RS and L&H cells, including recent knowledge about transforming mechanisms and signaling pathways that contribute to the antiapoptotic phenotype displayed by H-RS and L&H cells. We also discuss major cellular and molecular mediators contributing to the establishment and maintenance of a reactive background in HL-affected tissues. We believe that an in-depth understanding of the pathogenesis of HL will eventually lead to the development of novel biologically based therapeutic strategies in the near future.
Supported by the Friedrich and Maria Sophie Morit sche Stiftung, the Deutsche Krebshilfe, and the Deutsche Forschungsgemeinschaft.
Authors' disclosures of potential conflicts of interest are found at the end of this article.
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