Literature DB >> 21235429

Novel mitogen-activated protein kinase kinase inhibitors.

Mark S Chapman1, Jeffrey N Miner.   

Abstract

INTRODUCTION: the development of new drugs over the last few decades has targeted specific proteins thought to be a key to the disease state. MAPK kinases 1 and 2 (commonly known as MEK1-2) represent such proteins as they lie downstream of important drug targets for oncology, such as EGFR, RAS and RAF. Several MEK1-2 inhibitors are currently in Phase I and II clinical trials in oncology. AREAS COVERED: this review of current literature and recent conferences provides a background on the RAS-RAF-MEK-ERK signaling pathway and a discussion of early MEK inhibitors. The potential of MEK1-2 inhibitors for the treatment of inflammation is briefly presented. Preclinical and early clinical results are discussed for MEK inhibitors currently in development. Completed clinical trials of MEK inhibitors in oncology include some disappointments as well as some promising signs of the value of these compounds and we discuss the potential for MEK inhibitors as monotherapy and their use in drug combinations. EXPERT OPINION: the utility of MEK inhibitors as anticancer agents will depend on careful patient selection based on the presence of mutations in genes such as KRAS and BRAF, the identification of additional predictive biomarkers, and an improved understanding of the benefit of drug combinations utilizing both established and emerging therapeutics.

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Year:  2011        PMID: 21235429     DOI: 10.1517/13543784.2011.548803

Source DB:  PubMed          Journal:  Expert Opin Investig Drugs        ISSN: 1354-3784            Impact factor:   6.206


  18 in total

1.  MAPK signaling cascades mediate distinct glucocorticoid resistance mechanisms in pediatric leukemia.

Authors:  Courtney L Jones; Christy M Gearheart; Susan Fosmire; Cristina Delgado-Martin; Nikki A Evensen; Karen Bride; Angela J Waanders; Faye Pais; Jinhua Wang; Teena Bhatla; Danielle S Bitterman; Simone R de Rijk; Wallace Bourgeois; Smita Dandekar; Eugene Park; Tamara M Burleson; Pillai Pallavi Madhusoodhan; David T Teachey; Elizabeth A Raetz; Michelle L Hermiston; Markus Müschen; Mignon L Loh; Stephen P Hunger; Jinghui Zhang; Michael J Garabedian; Christopher C Porter; William L Carroll
Journal:  Blood       Date:  2015-08-31       Impact factor: 22.113

Review 2.  Resolution of inflammation: a new therapeutic frontier.

Authors:  James N Fullerton; Derek W Gilroy
Journal:  Nat Rev Drug Discov       Date:  2016-03-29       Impact factor: 84.694

3.  BRAF mutation is associated with a specific cell type with features suggestive of senescence in ovarian serous borderline (atypical proliferative) tumors.

Authors:  Felix Zeppernick; Laura Ardighieri; Charlotte G Hannibal; Russell Vang; Jette Junge; Susanne K Kjaer; Rugang Zhang; Robert J Kurman; Ie-Ming Shih
Journal:  Am J Surg Pathol       Date:  2014-12       Impact factor: 6.394

Review 4.  Rational selection of biomarker driven therapies for gynecologic cancers: The more we know, the more we know we don't know.

Authors:  Joyce Liu; Shannon N Westin
Journal:  Gynecol Oncol       Date:  2016-04       Impact factor: 5.482

Review 5.  Personalized therapy in endometrial cancer: challenges and opportunities.

Authors:  Shannon N Westin; Russell R Broaddus
Journal:  Cancer Biol Ther       Date:  2012-01-01       Impact factor: 4.742

Review 6.  Mitogen-activated protein kinase phosphatase (MKP)-1 in immunology, physiology, and disease.

Authors:  Lyn M Wancket; W Joshua Frazier; Yusen Liu
Journal:  Life Sci       Date:  2011-12-13       Impact factor: 5.037

7.  Antitumor activity of the MEK inhibitor TAK-733 against melanoma cell lines and patient-derived tumor explants.

Authors:  Lindsey N Micel; John J Tentler; Aik-Choon Tan; Heather M Selby; Kelsey L Brunkow; Kelli M Robertson; S Lindsey Davis; Peter J Klauck; Todd M Pitts; Esha Gangolli; Robyn Fabrey; Shawn M O'Connell; Patrick W Vincent; S Gail Eckhardt
Journal:  Mol Cancer Ther       Date:  2014-11-05       Impact factor: 6.261

8.  Evaluation of phosphatidylinositol-3-kinase catalytic subunit (PIK3CA) and epidermal growth factor receptor (EGFR) gene mutations in pancreaticobiliary adenocarcinoma.

Authors:  Guy A Weiss; Michael R Rossi; Nikhil I Khushalani; Ken Lo; John F Gibbs; Anubha Bharthuar; John K Cowell; Renuka Iyer
Journal:  J Gastrointest Oncol       Date:  2013-03

9.  Signature of microsatellite instability, KRAS and BRAF gene mutations in German patients with locally advanced rectal adenocarcinoma before and after neoadjuvant 5-FU radiochemotherapy.

Authors:  Melanie Demes; Stefanie Scheil-Bertram; Holger Bartsch; Annette Fisseler-Eckhoff
Journal:  J Gastrointest Oncol       Date:  2013-06

10.  Mechanism of MEK inhibition determines efficacy in mutant KRAS- versus BRAF-driven cancers.

Authors:  Georgia Hatzivassiliou; Jacob R Haling; Huifen Chen; Kyung Song; Steve Price; Robert Heald; Joanne F M Hewitt; Mark Zak; Ariana Peck; Christine Orr; Mark Merchant; Klaus P Hoeflich; Jocelyn Chan; Shiuh-Ming Luoh; Daniel J Anderson; Mary J C Ludlam; Christian Wiesmann; Mark Ultsch; Lori S Friedman; Shiva Malek; Marcia Belvin
Journal:  Nature       Date:  2013-08-11       Impact factor: 49.962

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