Literature DB >> 11927284

Unraveling the complexities of the Raf/MAP kinase pathway for pharmacological intervention.

Roman Herrera1, Judith S Sebolt-Leopold.   

Abstract

The Ras-MAP kinase pathway has attracted much attention from academic and pharmaceutical laboratories because of its central role in regulating tumor cell growth and survival, differentiation and angiogenesis. Although the central players in this pathway -Ras, Raf, and MEK - have been well studied, how best to exploit them for therapeutic gain has eluded oncology researchers in the past. Several small-molecule inhibitors that target specific steps of the MAP kinase cascade have recently entered the clinical arena. While we await answers on their ultimate therapeutic use, the availability of translational assays for monitoring target suppression will no doubt play a significant role in optimizing our chances of success.

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Year:  2002        PMID: 11927284     DOI: 10.1016/s1471-4914(02)02307-9

Source DB:  PubMed          Journal:  Trends Mol Med        ISSN: 1471-4914            Impact factor:   11.951


  16 in total

Review 1.  Mitogen activated protein (MAP) kinase signal transduction pathways and novel anti-inflammatory targets.

Authors:  D W Hommes; M P Peppelenbosch; S J H van Deventer
Journal:  Gut       Date:  2003-01       Impact factor: 23.059

Review 2.  Molecular genesis of non-muscle-invasive urothelial carcinoma (NMIUC).

Authors:  Courtney Pollard; Steven C Smith; Dan Theodorescu
Journal:  Expert Rev Mol Med       Date:  2010-03-25       Impact factor: 5.600

3.  A role for K-ras in conferring resistance to the MEK inhibitor, CI-1040.

Authors:  Yuli Wang; Keri Van Becelaere; Ping Jiang; Sally Przybranowski; Charles Omer; Judith Sebolt-Leopold
Journal:  Neoplasia       Date:  2005-04       Impact factor: 5.715

4.  Identification of Raf-1 S471 as a novel phosphorylation site critical for Raf-1 and B-Raf kinase activities and for MEK binding.

Authors:  Jun Zhu; Vitaly Balan; Agnieszka Bronisz; Karina Balan; Hengrui Sun; Deborah T Leicht; Zhijun Luo; Jun Qin; Joseph Avruch; Guri Tzivion
Journal:  Mol Biol Cell       Date:  2005-08-10       Impact factor: 4.138

5.  Mogrol represents a novel leukemia therapeutic, via ERK and STAT3 inhibition.

Authors:  Can Liu; Yan Zeng; Long-Hai Dai; Tian-Yu Cai; Yue-Ming Zhu; De-Quan Dou; Lan-Qing Ma; Yuan-Xia Sun
Journal:  Am J Cancer Res       Date:  2015-03-15       Impact factor: 6.166

6.  Characterization of an ERK-binding domain in microphthalmia-associated transcription factor and differential inhibition of ERK2-mediated substrate phosphorylation.

Authors:  Douglas M Molina; Seema Grewal; Lee Bardwell
Journal:  J Biol Chem       Date:  2005-10-24       Impact factor: 5.157

Review 7.  Overcoming resistance to molecularly targeted anticancer therapies: Rational drug combinations based on EGFR and MAPK inhibition for solid tumours and haematologic malignancies.

Authors:  Giampaolo Tortora; Roberto Bianco; Gennaro Daniele; Fortunato Ciardiello; James A McCubrey; Maria Rosaria Ricciardi; Ludovica Ciuffreda; Francesco Cognetti; Agostino Tafuri; Michele Milella
Journal:  Drug Resist Updat       Date:  2007-05-07       Impact factor: 18.500

8.  The transcriptional response to Raf activation is almost completely dependent on Mitogen-activated Protein Kinase Kinase activity and shows a major autocrine component.

Authors:  Almut Schulze; Barbara Nicke; Patricia H Warne; Simon Tomlinson; Julian Downward
Journal:  Mol Biol Cell       Date:  2004-04-16       Impact factor: 4.138

Review 9.  Raf kinases: function, regulation and role in human cancer.

Authors:  Deborah T Leicht; Vitaly Balan; Alexander Kaplun; Vinita Singh-Gupta; Ludmila Kaplun; Melissa Dobson; Guri Tzivion
Journal:  Biochim Biophys Acta       Date:  2007-05-22

10.  Protein and lipid kinase inhibitors as targeted anticancer agents of the Ras/Raf/MEK and PI3K/PKB pathways.

Authors:  Carlos García-Echeverría
Journal:  Purinergic Signal       Date:  2008-06-04       Impact factor: 3.765

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