Literature DB >> 11706400

Farnesyltransferase inhibitors.

S M Hahn1, E Bernhard, W G McKenna.   

Abstract

The targeting of molecular abnormalities in neoplasms may provide an opportunity to improve the selectivity of cancer therapy. Ras mutations are a common genetic event in human cancers. Other genetic changes in tumors can signal through ras-dependent pathways as well. The targeting of ras through the inhibition of Ras protein farnesylation is one new cancer treatment strategy under clinical evaluation. Several farnesyltransferase inhibitors (FTIs) have been evaluated in phase I trials. The toxicity and maximally tolerated doses of several FTIs have been determined, and clinical trials are underway to evaluate FTIs in combination with conventional cytotoxic chemotherapy agents. Also underway are attempts to develop assays to measure the biological effects of the FTI in patients. Inhibition of farnesylation of a number of surrogate markers are currently being investigated. These efforts may provide insight into the mechanism of action of these compounds and lead to improved patient selection for clinical trials. Copyright 2001 by W.B. Saunders Company.

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Year:  2001        PMID: 11706400     DOI: 10.1016/s0093-7754(01)90286-6

Source DB:  PubMed          Journal:  Semin Oncol        ISSN: 0093-7754            Impact factor:   4.929


  2 in total

1.  Use of inhibitors in the study of MAP kinases.

Authors:  Kimberly Burkhard; Paul Shapiro
Journal:  Methods Mol Biol       Date:  2010

2.  The synergistic combination of the farnesyl transferase inhibitor lonafarnib and paclitaxel enhances tubulin acetylation and requires a functional tubulin deacetylase.

Authors:  Adam I Marcus; Jun Zhou; Aurora O'Brate; Ernest Hamel; Jason Wong; Michael Nivens; Adel El-Naggar; Tso-Pang Yao; Fadlo R Khuri; Paraskevi Giannakakou
Journal:  Cancer Res       Date:  2005-05-01       Impact factor: 12.701

  2 in total

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