Literature DB >> 18020980

Selective Raf inhibition in cancer therapy.

Vladimir Khazak1, Igor Astsaturov, Ilya G Serebriiskii, Erica A Golemis.   

Abstract

Over the past 5 years, the Raf kinase family has emerged as a promising target for protein-directed cancer therapy development. The goal of this review is to first provide a concise summary of the data validating Raf proteins as high-interest therapeutic targets. The authors then outline the mode of action of Raf kinases, emphasizing how Raf activities and protein interactions suggest specific approaches to inhibiting Raf. The authors then summarize the set of drugs, antisense reagents and antibodies available or in development for therapeutically targeting Raf or Raf-related proteins, as well as existing strategies combining these and other therapeutic agents. Finally, the authors discuss recent results from systems biology analyses that have the potential to increasingly guide the intelligent selection of combination therapies involving Raf-targeting agents and other therapeutics.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 18020980      PMCID: PMC2720036          DOI: 10.1517/14728222.11.12.1587

Source DB:  PubMed          Journal:  Expert Opin Ther Targets        ISSN: 1472-8222            Impact factor:   6.902


  202 in total

1.  A phase II trial of 17-(Allylamino)-17-demethoxygeldanamycin in patients with papillary and clear cell renal cell carcinoma.

Authors:  Ellen A Ronnen; G Varuni Kondagunta; Nicole Ishill; Suzanne M Sweeney; John K Deluca; Lawrence Schwartz; Jennifer Bacik; Robert J Motzer
Journal:  Invest New Drugs       Date:  2006-11       Impact factor: 3.850

Review 2.  [BRAF initiating mutations in the papillary thyroid carcinoma].

Authors:  Dagmara Rusinek; Elzbieta Gubała
Journal:  Endokrynol Pol       Date:  2006 Jul-Aug       Impact factor: 1.582

3.  Mutation analysis of the BRAF, ARAF and RAF-1 genes in human colorectal adenocarcinomas.

Authors:  Karin Fransén; Maria Klintenäs; Anna Osterström; Jan Dimberg; Hans-Jürg Monstein; Peter Söderkvist
Journal:  Carcinogenesis       Date:  2003-12-19       Impact factor: 4.944

Review 4.  Targeting the function of the HER2 oncogene in human cancer therapeutics.

Authors:  M M Moasser
Journal:  Oncogene       Date:  2007-05-07       Impact factor: 9.867

5.  Sorafenib with interferon alfa-2b as first-line treatment of advanced renal carcinoma: a phase II study of the Southwest Oncology Group.

Authors:  Christopher W Ryan; Bryan H Goldman; Primo N Lara; Philip C Mack; Tomasz M Beer; Catherine M Tangen; Dianne Lemmon; Chong-Xian Pan; Harry A Drabkin; E David Crawford
Journal:  J Clin Oncol       Date:  2007-08-01       Impact factor: 44.544

6.  Targeting BRAFV600E in thyroid carcinoma: therapeutic implications.

Authors:  Constantine S Mitsiades; Joseph Negri; Ciaran McMullan; Douglas W McMillin; Elias Sozopoulos; Galinos Fanourakis; Gerassimos Voutsinas; Sophia Tseleni-Balafouta; Vassiliki Poulaki; David Batt; Nicholas Mitsiades
Journal:  Mol Cancer Ther       Date:  2007-03       Impact factor: 6.261

Review 7.  Her signaling in pancreatic cancer.

Authors:  Barbara Burtness
Journal:  Expert Opin Biol Ther       Date:  2007-06       Impact factor: 4.388

8.  BAY 43-9006 exhibits broad spectrum oral antitumor activity and targets the RAF/MEK/ERK pathway and receptor tyrosine kinases involved in tumor progression and angiogenesis.

Authors:  Scott M Wilhelm; Christopher Carter; Liya Tang; Dean Wilkie; Angela McNabola; Hong Rong; Charles Chen; Xiaomei Zhang; Patrick Vincent; Mark McHugh; Yichen Cao; Jaleel Shujath; Susan Gawlak; Deepa Eveleigh; Bruce Rowley; Li Liu; Lila Adnane; Mark Lynch; Daniel Auclair; Ian Taylor; Rich Gedrich; Andrei Voznesensky; Bernd Riedl; Leonard E Post; Gideon Bollag; Pamela A Trail
Journal:  Cancer Res       Date:  2004-10-01       Impact factor: 13.312

9.  Raf-1 activation disrupts its binding to keratins during cell stress.

Authors:  Nam-On Ku; Haian Fu; M Bishr Omary
Journal:  J Cell Biol       Date:  2004-08-16       Impact factor: 10.539

10.  Amplification of both c-myc and c-raf-1 oncogenes in a human osteosarcoma.

Authors:  S Ikeda; H Sumii; K Akiyama; S Watanabe; S Ito; H Inoue; H Takechi; G Tanabe; T Oda
Journal:  Jpn J Cancer Res       Date:  1989-01
View more
  23 in total

1.  A brain-penetrant RAF dimer antagonist for the noncanonical BRAF oncoprotein of pediatric low-grade astrocytomas.

Authors:  Yu Sun; John A Alberta; Catherine Pilarz; David Calligaris; Emily J Chadwick; Shakti H Ramkissoon; Lori A Ramkissoon; Veronica Matia Garcia; Emanuele Mazzola; Liliana Goumnerova; Michael Kane; Zhan Yao; Mark W Kieran; Keith L Ligon; William C Hahn; Levi A Garraway; Neal Rosen; Nathanael S Gray; Nathalie Y Agar; Sara J Buhrlage; Rosalind A Segal; Charles D Stiles
Journal:  Neuro Oncol       Date:  2017-06-01       Impact factor: 12.300

2.  Analyses of the oncogenic BRAFD594G variant reveal a kinase-independent function of BRAF in activating MAPK signaling.

Authors:  Nicholas J Cope; Borna Novak; Zhiwei Liu; Maria Cavallo; Amber Y Gunderwala; Matthew Connolly; Zhihong Wang
Journal:  J Biol Chem       Date:  2020-01-12       Impact factor: 5.157

3.  Reactivation of mitogen-activated protein kinase (MAPK) pathway by FGF receptor 3 (FGFR3)/Ras mediates resistance to vemurafenib in human B-RAF V600E mutant melanoma.

Authors:  Vipin Yadav; Xiaoyi Zhang; Jiangang Liu; Shawn Estrem; Shuyu Li; Xue-Qian Gong; Sean Buchanan; James R Henry; James J Starling; Sheng-Bin Peng
Journal:  J Biol Chem       Date:  2012-06-22       Impact factor: 5.157

Review 4.  Practical guidelines for therapeutic drug monitoring of anticancer tyrosine kinase inhibitors: focus on the pharmacokinetic targets.

Authors:  Huixin Yu; Neeltje Steeghs; Cynthia M Nijenhuis; Jan H M Schellens; Jos H Beijnen; Alwin D R Huitema
Journal:  Clin Pharmacokinet       Date:  2014-04       Impact factor: 6.447

5.  RAF translocations expand cancer targets.

Authors:  Martin McMahon
Journal:  Nat Med       Date:  2010-07       Impact factor: 53.440

6.  Raf family kinases: old dogs have learned new tricks.

Authors:  David Matallanas; Marc Birtwistle; David Romano; Armin Zebisch; Jens Rauch; Alexander von Kriegsheim; Walter Kolch
Journal:  Genes Cancer       Date:  2011-03

7.  Coordinate direct input of both KRAS and IGF1 receptor to activation of PI3 kinase in KRAS-mutant lung cancer.

Authors:  Miriam Molina-Arcas; David C Hancock; Clare Sheridan; Madhu S Kumar; Julian Downward
Journal:  Cancer Discov       Date:  2013-03-01       Impact factor: 39.397

8.  Genetic and functional characterization of putative Ras/Raf interaction inhibitors in C. elegans and mammalian cells.

Authors:  Vanessa González-Pérez; David J Reiner; Jamie K Alan; Cicely Mitchell; Lloyd J Edwards; Vladimir Khazak; Channing J Der; Adrienne D Cox
Journal:  J Mol Signal       Date:  2010-02-23

Review 9.  Stamping out RAF and MEK1/2 to inhibit the ERK1/2 pathway: an emerging threat to anticancer therapy.

Authors:  R Mandal; S Becker; K Strebhardt
Journal:  Oncogene       Date:  2015-09-14       Impact factor: 9.867

Review 10.  Newly developed strategies for improving sensitivity to radiation by targeting signal pathways in cancer therapy.

Authors:  Miao Ding; Erlong Zhang; Rong He; Xingyong Wang
Journal:  Cancer Sci       Date:  2013-09-23       Impact factor: 6.716

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.