Literature DB >> 12769711

Sch-66336 (sarasar) and other benzocycloheptapyridyl farnesyl protein transferase inhibitors: discovery, biology and clinical observations.

Arthur G Taveras1, Paul Kirschmeier, Charles M Baum.   

Abstract

Farnesyl Protein Transferase as a target for therapeutic intervention is currently under investigation in human clinical trials. Sch-66336 (sarasar), a benzocycloheptapyridyl Farnesyl Transferase Inhibitor (FTI), has been found to be effective in cellular proliferation assays and in in vivo oncology models both as a single agent and in combination with other anti-cancer agents. Clinically, early evidence is being generated that suggests efficacy in humans, particularly in patients with leukemia. Herein, we review the biology of FPT, the discovery of Sch-66336 and other benzocycloheptapyridyl FTIs, and the clinical evaluation of Sch-66336 for the treatment of leukemia and solid tumors.

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Year:  2003        PMID: 12769711     DOI: 10.2174/1568026033452104

Source DB:  PubMed          Journal:  Curr Top Med Chem        ISSN: 1568-0266            Impact factor:   3.295


  9 in total

1.  Finding a needle in the haystack: computational modeling of Mg2+ binding in the active site of protein farnesyltransferase.

Authors:  Yue Yang; Dhruva K Chakravorty; Kenneth M Merz
Journal:  Biochemistry       Date:  2010-11-09       Impact factor: 3.162

2.  Computational studies of the farnesyltransferase ternary complex part I: substrate binding.

Authors:  Guanglei Cui; Bing Wang; Kenneth M Merz
Journal:  Biochemistry       Date:  2005-12-20       Impact factor: 3.162

3.  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

4.  Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome.

Authors:  Brian C Capell; Michael R Erdos; James P Madigan; James J Fiordalisi; Renee Varga; Karen N Conneely; Leslie B Gordon; Channing J Der; Adrienne D Cox; Francis S Collins
Journal:  Proc Natl Acad Sci U S A       Date:  2005-08-29       Impact factor: 11.205

5.  Computational studies of the farnesyltransferase ternary complex part II: the conformational activation of farnesyldiphosphate.

Authors:  Guanglei Cui; Kenneth M Merz
Journal:  Biochemistry       Date:  2007-10-06       Impact factor: 3.162

6.  A phase I safety, pharmacological, and biological study of the farnesyl protein transferase inhibitor, lonafarnib (SCH 663366), in combination with cisplatin and gemcitabine in patients with advanced solid tumors.

Authors:  Laura Q M Chow; S Gail Eckhardt; Cindy L O'Bryant; Mary Kay Schultz; Mark Morrow; Stacy Grolnic; Michele Basche; Lia Gore
Journal:  Cancer Chemother Pharmacol       Date:  2007-12-06       Impact factor: 3.333

Review 7.  Molecularly targeted therapy for pediatric brain tumors.

Authors:  Warren K E
Journal:  J Neurooncol       Date:  2005-12       Impact factor: 4.506

Review 8.  Farnesyltransferase inhibitors in myelodysplastic syndrome.

Authors:  E J Feldman
Journal:  Curr Hematol Malig Rep       Date:  2006-03       Impact factor: 4.213

9.  Immature and mature species of the human Prostacyclin Receptor are ubiquitinated and targeted to the 26S proteasomal or lysosomal degradation pathways, respectively.

Authors:  Peter D Donnellan; B Therese Kinsella
Journal:  J Mol Signal       Date:  2009-09-25
  9 in total

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