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Farnesyltransferase Inhibitors and Rapamycin in the Treatment of Multiple Myeloma

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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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Keywords: CAAX binding site; CCI-779; STAT3 tyrosine phosphorylation; Tipifarnib; haematological malignancies; mTOR Kinase pathway

Document Type: Research Article

Affiliations: Myeloma Institute for Research and Therapy University of Arkansas for Medical Sciences, Little Rock, AR, USA.

Publication date: 2006-12-01

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  • Current Pharmaceutical Biotechnology aims to cover all the latest and outstanding developments in Pharmaceutical Biotechnology. Each issue of the journal contains a series of timely in-depth reviews written by leaders in the field covering a range of current topics in both pre-clinical and clinical areas of Pharmaceutical Biotechnology. Current Pharmaceutical Biotechnology is an essential journal for academic, clinical, government and pharmaceutical scientists who wish to be kept informed and up-to-date with the latest and most important developments.
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