Literature DB >> 12369850

Rationale for Ras and raf-kinase as a target for cancer therapeutics.

Michelle Nottage1, Lillian L Siu.   

Abstract

Improvements in our understanding of the intrinsic aberrancies in cancer cells have enabled the design and development of novel therapeutics that specifically target these changes. Among the many complex cellular pathways and mechanisms which have been unveiled by new molecular techniques, RAS-mediated signal transduction is one met with tremendous research interests. Activation of RAS initiates several signaling cascades, of which the RAS-RAF-MEK-ERK pathway is among the better delineated, and is the main focus of this review. Other cellular consequences of RAS activation including interactions with the RHO-family proteins, the PI3-kinase pathway, and other mitogen activated protein kinase cascades, will be discussed. The intricate balance and coordination of multiple RAS-mediated signals lead to ultimate effects on cell growth, differentiation, cycling and survival. Pharmacological strategies such as analog development, synthesis of small molecule inhibitors, antisense technology, and vaccine therapy have been utilized to intervene with key RAS-signaling proteins, in an attempt to provide rational therapeutic solutions in malignant diseases.

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Year:  2002        PMID: 12369850     DOI: 10.2174/1381612023393107

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  11 in total

1.  Reduction of Raf kinase inhibitor protein expression by Bcr-Abl contributes to chronic myelogenous leukemia proliferation.

Authors:  Tomonari Takemura; Satoki Nakamura; Daisuke Yokota; Isao Hirano; Takaaki Ono; Kazuyuki Shigeno; Shinya Fujisawa; Kazunori Ohnishi
Journal:  J Biol Chem       Date:  2009-12-22       Impact factor: 5.157

2.  Loss of Raf kinase inhibitor protein promotes cell proliferation and migration of human hepatoma cells.

Authors:  Han Chu Lee; Bo Tian; John M Sedivy; Jack R Wands; Miran Kim
Journal:  Gastroenterology       Date:  2006-10       Impact factor: 22.682

3.  Mechanisms of disease: epithelial-mesenchymal transition--does cellular plasticity fuel neoplastic progression?

Authors:  Eva A Turley; Mandana Veiseh; Derek C Radisky; Mina J Bissell
Journal:  Nat Clin Pract Oncol       Date:  2008-03-18

4.  The effects of a novel MEK inhibitor PD184161 on MEK-ERK signaling and growth in human liver cancer.

Authors:  Patrick J Klein; C Max Schmidt; Chad A Wiesenauer; Jennifer N Choi; Earl A Gage; Michele T Yip-Schneider; Eric A Wiebke; Yufang Wang; Charles Omer; Judith S Sebolt-Leopold
Journal:  Neoplasia       Date:  2006-01       Impact factor: 5.715

5.  Effect of the DEF motif on phosphorylation of peptide substrates by ERK.

Authors:  Neychelle Fernandes; Nancy L Allbritton
Journal:  Biochem Biophys Res Commun       Date:  2009-07-15       Impact factor: 3.575

6.  Upregulation of the Catalytic Telomerase Subunit by the Transcription Factor ER81 and Oncogenic HER2/Neu, Ras, or Raf.

Authors:  Basem S Goueli; Ralf Janknecht
Journal:  Mol Cell Biol       Date:  2004-01       Impact factor: 4.272

7.  Use of docking peptides to design modular substrates with high efficiency for mitogen-activated protein kinase extracellular signal-regulated kinase.

Authors:  Neychelle Fernandes; Denise E Bailey; David L Vanvranken; Nancy L Allbritton
Journal:  ACS Chem Biol       Date:  2007-10-06       Impact factor: 5.100

Review 8.  MicroRNAs as Mediators of Resistance Mechanisms to Small-Molecule Tyrosine Kinase Inhibitors in Solid Tumours.

Authors:  Michele Ghidini; Jens C Hahne; Melissa Frizziero; Gianluca Tomasello; Francesco Trevisani; Andrea Lampis; Rodolfo Passalacqua; Nicola Valeri
Journal:  Target Oncol       Date:  2018-08       Impact factor: 4.493

9.  Absence of mutations in the coding sequence of the potential tumor suppressor 3pK in metastatic melanoma.

Authors:  Roland Houben; Jürgen C Becker; Ulf R Rapp
Journal:  J Carcinog       Date:  2005-12-20

10.  Overexpression of tumor necrosis factor receptor-associated protein 1 (TRAP1), leads to mitochondrial aberrations in mouse fibroblast NIH/3T3 cells.

Authors:  Chang-Nim Im; Jeong-Sun Seo
Journal:  BMB Rep       Date:  2014-05       Impact factor: 4.778

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