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2000
Volume 7, Issue 6
  • ISSN: 1389-2010
  • E-ISSN: 1873-4316

Abstract

Multiple myeloma (MM) is a B-cell malignancy characterized by an accumulation of long-lived neoplastic plasma cells (PC) within the bone marrow (BM). Novel treatments are not only targeting myeloma cells but also directly interfere with myeloma-stromal cell interactions, interrupting signal transduction pathways. Farnesyltransferase inhibitors (FTIs) and rapamycin represent novel classes of signal transduction inhibitors targeting principally Ras/MAPK and PI3K/Akt pathway. Pre-clinical and early clinical reports are presented in this study.

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/content/journals/cpb/10.2174/138920106779116838
2006-12-01
2025-04-09
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