Literature DB >> 14763129

Raf pathway inhibitors in oncology.

Gideon Bollag1, Scott Freeman, John F Lyons, Leonard E Post.   

Abstract

Recognition of the importance of the Raf pathway in the proliferation and survival of tumor cells recently increased with the discovery of activating BRAF mutations in human tumors. Therefore, in addition to a role in controlling tumors with Ras mutations and activated growth factor receptors, inhibitors of the Raf pathway may harbor therapeutic potential in tumors carrying a BRAF oncogene. A variety of agents have been discovered that interfere with the Raf pathway, including antisense oligonucleotides and small molecules. These inhibitors block the expression of Raf protein, block Ras/Raf interaction, block its kinase activity, or block the kinase activity of the Raf target protein mitogen-activated protein kinase kinase. Raf pathway inhibitors that are currently undergoing clinical evaluation show promising signs of anticancer efficacy with a very tolerable safety profile. Indeed, the Raf inhibitor BAY-43-9006 recently entered phase III clinical trials. Here, we review the current development status of potential Raf pathway therapeutics.

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Year:  2003        PMID: 14763129

Source DB:  PubMed          Journal:  Curr Opin Investig Drugs        ISSN: 1472-4472


  15 in total

1.  Targeting mitogen-activated protein kinase/extracellular signal-regulated kinase kinase in the mutant (V600E) B-Raf signaling cascade effectively inhibits melanoma lung metastases.

Authors:  Arati Sharma; Melissa A Tran; Shile Liang; Arun K Sharma; Shantu Amin; Charles D Smith; Cheng Dong; Gavin P Robertson
Journal:  Cancer Res       Date:  2006-08-15       Impact factor: 12.701

2.  Phase 1 study of sorafenib in combination with bortezomib in patients with advanced malignancies.

Authors:  Shaji K Kumar; James Jett; Randolph Marks; Ronald Richardson; Fernando Quevedo; Timothy Moynihan; Gary Croghan; Svetomir N Markovic; Keith C Bible; Rui Qin; Angelina Tan; Julian Molina; Scott H Kaufmann; Charles Erlichman; Alex A Adjei
Journal:  Invest New Drugs       Date:  2013-07-26       Impact factor: 3.850

3.  A critical function for B-Raf at multiple stages of myelopoiesis.

Authors:  Tamihiro Kamata; Jing Kang; Tzong-Hae Lee; Leszek Wojnowski; Catrin A Pritchard; Andrew D Leavitt
Journal:  Blood       Date:  2005-03-22       Impact factor: 22.113

4.  Characterization of ATP-independent ERK inhibitors identified through in silico analysis of the active ERK2 structure.

Authors:  Fengming Chen; Chad N Hancock; Alba T Macias; Joseph Joh; Kimberly Still; Shijun Zhong; Alexander D MacKerell; Paul Shapiro
Journal:  Bioorg Med Chem Lett       Date:  2006-09-26       Impact factor: 2.823

5.  Peroxynitrite activates ERK via Raf-1 and MEK, independently from EGF receptor and p21Ras in H9C2 cardiomyocytes.

Authors:  B Pesse; S Levrand; F Feihl; B Waeber; B Gavillet; P Pacher; L Liaudet
Journal:  J Mol Cell Cardiol       Date:  2005-05       Impact factor: 5.000

Review 6.  Ras oncogenes: split personalities.

Authors:  Antoine E Karnoub; Robert A Weinberg
Journal:  Nat Rev Mol Cell Biol       Date:  2008-07       Impact factor: 94.444

Review 7.  Vemurafenib: the first drug approved for BRAF-mutant cancer.

Authors:  Gideon Bollag; James Tsai; Jiazhong Zhang; Chao Zhang; Prabha Ibrahim; Keith Nolop; Peter Hirth
Journal:  Nat Rev Drug Discov       Date:  2012-10-12       Impact factor: 84.694

8.  Ras signaling influences permissiveness of malignant peripheral nerve sheath tumor cells to oncolytic herpes.

Authors:  Faris Farassati; Weihong Pan; Farnaz Yamoutpour; Susann Henke; Mark Piedra; Silke Frahm; Said Al-Tawil; Wells I Mangrum; Luis F Parada; Samuel D Rabkin; Robert L Martuza; Andreas Kurtz
Journal:  Am J Pathol       Date:  2008-11-06       Impact factor: 4.307

9.  Anatomic site-specific patterns of gene copy number gains in skin, mucosal, and uveal melanomas detected by fluorescence in situ hybridization.

Authors:  Katharina Glatz-Krieger; Mona Pache; Coya Tapia; Alain Fuchs; Spasenija Savic; Dieter Glatz; Michael Mihatsch; Peter Meyer
Journal:  Virchows Arch       Date:  2006-03-08       Impact factor: 4.064

10.  Using Caenorhabditis elegans as a model organism for evaluating extracellular signal-regulated kinase docking domain inhibitors.

Authors:  Fengming Chen; Alexander D Mackerell; Yuan Luo; Paul Shapiro
Journal:  J Cell Commun Signal       Date:  2008-12-23       Impact factor: 5.782

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