Literature DB >> 15013521

Perspectives on farnesyl transferase inhibitors in cancer therapy.

Julien Mazieres1, Anne Pradines, Gilles Favre.   

Abstract

The discovery that the transforming activity of oncogenic Ras depends upon its post-translational farnesylation has led to the development of farnesyl transferase inhibitors (FTIs). FTIs inhibit the growth of ras-transformed cells in vitro and induce tumor regression in Ras-dependent tumors. Currently, FTIs are undergoing clinical trials in various solid or hematological malignancies. In this review, we will summarize our current knowledge on cellular effect and molecular mechanism of FTIs. We will then describe recent clinical trials and propose some clues for their interpretation. Based on pre-clinical findings, we will emphasize on the optimal use of FTIs in anti-cancer strategy and lastly, we will insist on the interest of combining FTIs with chemotherapy, radiotherapy or other targeted agents.

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Year:  2004        PMID: 15013521     DOI: 10.1016/j.canlet.2003.08.033

Source DB:  PubMed          Journal:  Cancer Lett        ISSN: 0304-3835            Impact factor:   8.679


  23 in total

Review 1.  Unraveling the mechanism of the farnesyltransferase enzyme.

Authors:  Sérgio Filipe Sousa; Pedro Alexandrino Fernandes; Maria João Ramos
Journal:  J Biol Inorg Chem       Date:  2004-12-21       Impact factor: 3.358

Review 2.  Targeted Cancer Therapies and QT Interval Prolongation: Unveiling the Mechanisms Underlying Arrhythmic Complications and the Need for Risk Stratification Strategies.

Authors:  Rezarta Cuni; Iris Parrini; Riccardo Asteggiano; Maria Rosa Conte
Journal:  Clin Drug Investig       Date:  2017-02       Impact factor: 2.859

3.  Structure-activity relationship studies on quorum sensing ComX(RO-E-2) pheromone.

Authors:  Masahiro Okada; Hisao Yamaguchi; Isao Sato; Soo Jeong Cho; David Dubnau; Youji Sakagami
Journal:  Bioorg Med Chem Lett       Date:  2006-12-23       Impact factor: 2.823

Review 4.  Statistical analysis, optimization, and prioritization of virtual screening parameters for zinc enzymes including the anthrax toxin lethal factor.

Authors:  Kimberly M Maize; Xia Zhang; Elizabeth Ambrose Amin
Journal:  Curr Top Med Chem       Date:  2014       Impact factor: 3.295

5.  Quantitative structure-activity relationship (QSAR) of indoloacetamides as inhibitors of human isoprenylcysteine carboxyl methyltransferase.

Authors:  Jo-Lene Leow; Rudi Baron; Patrick J Casey; Mei-Lin Go
Journal:  Bioorg Med Chem Lett       Date:  2006-11-15       Impact factor: 2.823

6.  Ras in cancer and developmental diseases.

Authors:  Alberto Fernández-Medarde; Eugenio Santos
Journal:  Genes Cancer       Date:  2011-03

7.  Role of isoprenylcysteine carboxylmethyltransferase-catalyzed methylation in Rho function and migration.

Authors:  Ian Cushman; Patrick J Casey
Journal:  J Biol Chem       Date:  2009-08-03       Impact factor: 5.157

8.  Imidazole-containing farnesyltransferase inhibitors: 3D quantitative structure-activity relationships and molecular docking.

Authors:  Aihua Xie; Srinivas Odde; Sivaprakasam Prasanna; Robert J Doerksen
Journal:  J Comput Aided Mol Des       Date:  2009-05-29       Impact factor: 3.686

Review 9.  Neurofibromatosis type 1: new insights into neurocognitive issues.

Authors:  Maria T Acosta; Gerard A Gioia; Alcino J Silva
Journal:  Curr Neurol Neurosci Rep       Date:  2006-03       Impact factor: 5.081

Review 10.  Biochemical and docking analysis of substrate interactions with polyisoprenylated methylated protein methyl esterase.

Authors:  R Duverna; S Y Ablordeppey; N S Lamango
Journal:  Curr Cancer Drug Targets       Date:  2010-09       Impact factor: 3.428

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