Literature DB >> 11566614

Farnesyl transferase inhibitors--a novel therapy for breast cancer.

S R Johnston1, L R Kelland.   

Abstract

Inhibitors of the enzyme farnesyl protein transferase prevent a key step in the post-translational processing of the Ras protein, and were developed initially as a therapeutic strategy to inhibit cell signalling in ras-transformed cells. As more has been learnt about the biological effects of farnesyl transferase inhibitors (FTIs) on cancer cells, it is clear that tumours without oncogenic ras mutations such as breast cancer may also be targets for FTI therapy. This article reviews the rationale for the development of FTIs, focussing on early preclinical data in breast cancer models together with preliminary results from the first phase II study of an FTI in advanced breast cancer.

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Year:  2001        PMID: 11566614     DOI: 10.1677/erc.0.0080227

Source DB:  PubMed          Journal:  Endocr Relat Cancer        ISSN: 1351-0088            Impact factor:   5.678


  9 in total

Review 1.  Preclinical and clinical evaluation of farnesyltransferase inhibitors.

Authors:  Charles Baum; Paul Kirschmeier
Journal:  Curr Oncol Rep       Date:  2003-03       Impact factor: 5.075

2.  Design and synthesis of non-hydrolyzable homoisoprenoid α-monofluorophosphonate inhibitors of PPAPDC family integral membrane lipid phosphatases.

Authors:  Thangaiah Subramanian; Hongmei Ren; Karunai Leela Subramanian; Manjula Sunkara; Fredrick O Onono; Andrew J Morris; H Peter Spielmann
Journal:  Bioorg Med Chem Lett       Date:  2014-08-12       Impact factor: 2.823

3.  Amide-substituted farnesylcysteine analogs as inhibitors of human isoprenylcysteine carboxyl methyltransferase.

Authors:  James L Donelson; Heather B Hodges; Daniel D Macdougall; Brian S Henriksen; Christine A Hrycyna; Richard A Gibbs
Journal:  Bioorg Med Chem Lett       Date:  2006-06-13       Impact factor: 2.823

4.  Tipifarnib-induced apoptosis in acute myeloid leukemia and multiple myeloma cells depends on Ca2+ influx through plasma membrane Ca2+ channels.

Authors:  Niranjan Yanamandra; Robert W Buzzeo; Mark Gabriel; Lori A Hazlehurst; Yelenis Mari; Darrin M Beaupre; Javier Cuevas
Journal:  J Pharmacol Exp Ther       Date:  2011-03-04       Impact factor: 4.030

5.  Lysyl oxidase inhibits ras-mediated transformation by preventing activation of NF-kappa B.

Authors:  Sébastien Jeay; Stefania Pianetti; Herbert M Kagan; Gail E Sonenshein
Journal:  Mol Cell Biol       Date:  2003-04       Impact factor: 4.272

Review 6.  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

Review 7.  Novel agents for the prevention of breast cancer: targeting transcription factors and signal transduction pathways.

Authors:  Qiang Shen; Powel H Brown
Journal:  J Mammary Gland Biol Neoplasia       Date:  2003-01       Impact factor: 2.673

8.  The bisphosphonate zoledronic acid impairs Ras membrane [correction of impairs membrane] localisation and induces cytochrome c release in breast cancer cells.

Authors:  S G Senaratne; J L Mansi; K W Colston
Journal:  Br J Cancer       Date:  2002-05-06       Impact factor: 7.640

Review 9.  The future of cytotoxic therapy: selective cytotoxicity based on biology is the key.

Authors:  Johann S de Bono; Anthony W Tolcher; Eric K Rowinsky
Journal:  Breast Cancer Res       Date:  2003-03-27       Impact factor: 6.466

  9 in total

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