Abstract
Multiple myeloma (MM) is a neoplasm of mature plasma cells [1], characterized by the accumulation of malignant cells in the bone marrow that are dedicated to the production of a monoclonal immunoglobulin [1]. It is also char acterized by osteolytic lesions [2], anemia, hyper calcemia and renal failure [3]. MM is responsible for approximately 10% of all hematological can cers [4] and its incidence is increasing, in part because of an aging trend in the world popula tion. Approximately half of all MM patients are older than 70 years and 20% of them are older than 80 years at diagnosis [5]. A major change in the treatment of MM occurred in the last decade, with the discovery of new therapeutic agents, such as immuno modulatory drugs (thalidomide and lenalido mide) and proteasome inhibitors (bortezomib) [6]. The use of these drugs, in different combi nations, improved the complete response rate in patients eligible for autologous hematopoietic stem cell transplantation, and has contributed to prolong progressionfree survival and to improve the quality of life of MM patients [7]. However, after more than 30 years of autologous hematopoietic stem cell transplantation use in MM treatment, this procedure is not consid ered curative [2]. Even with multiple approaches and promising therapeutic agents, MM remains an incurable disease [3,8]. Thus, a better under standing of the molecular pathogenesis of MM is essential for the development of novel drugs capable of overcoming relapses and improving survival in MM.
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