Literature DB >> 24756797

Trametinib.

Robert Zeiser1.   

Abstract

The mitogen-activated protein kinase (MEK MAPK/ERK kinase) signaling pathways play a critical role in regulation of diverse cellular activities, including survival, differentiation, proliferation, motility, and angiogenesis. Therefore, MEK inhibition was recognized as a promising target for antineoplastic therapy. While multiple MEK inhibitors have been tested clinically only trametinib (GSK1120212), an oral MEK inhibitor which is selective for MEK1 and MEK2 has shown promising activity in several clinical trials on melanoma and colorectal cancer and it is being evaluated by the FDA for the treatment of metastatic melanoma. Mechanistically it was shown that trametinib induces cell cycle arrest in vitro. In this overview, important preclinical and clinical data for trametinib are presented including mechanism-based in vitro studies as well as findings from different clinical studies. Future clinical trial in different solid tumor entities will define the therapeutic role of this targeted therapy approach, possibly as a combination with other targeted therapies such as BRAF inhibitors.

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Year:  2014        PMID: 24756797     DOI: 10.1007/978-3-642-54490-3_15

Source DB:  PubMed          Journal:  Recent Results Cancer Res        ISSN: 0080-0015


  9 in total

1.  Genotype-Guided Medical Treatment of an Arteriovenous Malformation in a Child.

Authors:  Ramrada Lekwuttikarn; Young H Lim; Shehla Admani; Keith A Choate; Joyce M C Teng
Journal:  JAMA Dermatol       Date:  2019-02-01       Impact factor: 10.282

2.  Resistance to Selumetinib (AZD6244) in colorectal cancer cell lines is mediated by p70S6K and RPS6 activation.

Authors:  Silvina Grasso; Elena Tristante; Miguel Saceda; Pablo Carbonell; Leticia Mayor-López; Mar Carballo-Santana; Estefanía Carrasco-García; Lourdes Rocamora-Reverte; Pilar García-Morales; Fernando Carballo; José A Ferragut; Isabel Martínez-Lacaci
Journal:  Neoplasia       Date:  2014-10-23       Impact factor: 5.715

3.  Activation of ERK1/2 Causes Pazopanib Resistance via Downregulation of DUSP6 in Synovial Sarcoma Cells.

Authors:  Nobuhiko Yokoyama; Tomoya Matsunobu; Yoshihiro Matsumoto; Jun-Ichi Fukushi; Makoto Endo; Mihoko Hatano; Akira Nabeshima; Suguru Fukushima; Seiji Okada; Yukihide Iwamoto
Journal:  Sci Rep       Date:  2017-03-28       Impact factor: 4.379

Review 4.  Mechanisms shaping the role of ERK1/2 in cellular senescence (Review).

Authors:  Junrong Zou; Tingting Lei; Pei Guo; Jason Yu; Qichao Xu; Yunfei Luo; Rong Ke; Deqiang Huang
Journal:  Mol Med Rep       Date:  2018-11-29       Impact factor: 2.952

Review 5.  Role of the Transcription Factor FOSL1 in Organ Development and Tumorigenesis.

Authors:  Vladimir V Sobolev; Asiat Z Khashukoeva; Olga E Evina; Natalia A Geppe; Svetlana N Chebysheva; Irina M Korsunskaya; Ekaterina Tchepourina; Alexandre Mezentsev
Journal:  Int J Mol Sci       Date:  2022-01-28       Impact factor: 5.923

Review 6.  KRAS as a Key Oncogene in the Clinical Precision Diagnosis and Treatment of Pancreatic Cancer.

Authors:  Manxiong Dai; Shaofeng Chen; Xiong Teng; Kang Chen; Wei Cheng
Journal:  J Cancer       Date:  2022-08-31       Impact factor: 4.478

7.  High EMT Signature Score of Invasive Non-Small Cell Lung Cancer (NSCLC) Cells Correlates with NFκB Driven Colony-Stimulating Factor 2 (CSF2/GM-CSF) Secretion by Neighboring Stromal Fibroblasts.

Authors:  Albin Rudisch; Matthew Richard Dewhurst; Luminita Gabriela Horga; Nina Kramer; Nathalie Harrer; Meng Dong; Heiko van der Kuip; Andreas Wernitznig; Andreas Bernthaler; Helmut Dolznig; Wolfgang Sommergruber
Journal:  PLoS One       Date:  2015-04-28       Impact factor: 3.240

8.  A phase I dose-escalation study of TAK-733, an investigational oral MEK inhibitor, in patients with advanced solid tumors.

Authors:  Alex A Adjei; Patricia LoRusso; Antoni Ribas; Jeffrey A Sosman; Anna Pavlick; Grace K Dy; Xiaofei Zhou; Esha Gangolli; Michelle Kneissl; Stephanie Faucette; Rachel Neuwirth; Viviana Bózon
Journal:  Invest New Drugs       Date:  2016-09-21       Impact factor: 3.850

9.  The newly identified MEK1 tyrosine phosphorylation target MACC1 is druggable by approved MEK1 inhibitors to restrict colorectal cancer metastasis.

Authors:  Dennis Kobelt; Daniel Perez-Hernandez; Claudia Fleuter; Mathias Dahlmann; Fabian Zincke; Janice Smith; Rebekka Migotti; Oliver Popp; Susen Burock; Wolfgang Walther; Gunnar Dittmar; Philipp Mertins; Ulrike Stein
Journal:  Oncogene       Date:  2021-07-10       Impact factor: 9.867

  9 in total

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