Literature DB >> 28011205

Macrocyclic MEK1/2 inhibitor with efficacy in a mouse model of cardiomyopathy caused by lamin A/C gene mutation.

Wei Wu1, Mahendra D Chordia2, Barry P Hart3, E Sathyajith Kumarasinghe2, Min K Ji2, Ajay Bhargava4, Michael W Lawlor5, Ji-Yeon Shin1, Fusako Sera6, Shunichi Homma6, Antoine Muchir1, Uday R Khire7, Howard J Worman8.   

Abstract

Signaling mediated by extracellular signal-regulated kinases 1 and 2 (ERK1/2) is involved in numerous cellular processes. Mitogen-activated protein kinase kinases (MEK1/2) catalyze the phosphorylation of ERK1/2, converting it into an active kinase that regulates the expression of numerous genes and cellular processes. Inhibitors of MEK1/2 have demonstrated preclinical and clinical efficacy in certain cancers and types of cardiomyopathy. We report the synthesis of a novel, allosteric, macrocyclic MEK1/2 inhibitor that potently inhibits ERK1/2 activity in cultured cells and tissues of mice after systemic administration. Mice with dilated cardiomyopathy caused by a lamin A/C gene mutation have abnormally increased cardiac ERK1/2 activity. In these mice, this novel MEK1/2 inhibitor is well tolerated, improves left ventricular systolic function, decreases left ventricular fibrosis, has beneficial effects on skeletal muscle structure and pathology and prolongs survival. The novel MEK1/2 inhibitor described herein may therefore find clinical utility in the treatment of this rare cardiomyopathy, other types of cardiomyopathy and cancers in humans.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Cardiomyopathy; Emery-Dreifuss muscular dystrophy; Extracellular signal-regulated kinase; Lamin; MEK inhibitor; Mitogen-activated protein kinase

Mesh:

Substances:

Year:  2016        PMID: 28011205      PMCID: PMC5291759          DOI: 10.1016/j.bmc.2016.12.014

Source DB:  PubMed          Journal:  Bioorg Med Chem        ISSN: 0968-0896            Impact factor:   3.641


  43 in total

1.  EMBOLIC COMPLICATIONS OF CARDIOMYOPATHY.

Authors:  J E COSNETT; D J PUDIFIN
Journal:  Br Heart J       Date:  1964-07

Review 2.  Laminopathies and the long strange trip from basic cell biology to therapy.

Authors:  Howard J Worman; Loren G Fong; Antoine Muchir; Stephen G Young
Journal:  J Clin Invest       Date:  2009-07-01       Impact factor: 14.808

3.  Design and synthesis of novel allosteric MEK inhibitor CH4987655 as an orally available anticancer agent.

Authors:  Yoshiaki Isshiki; Yasunori Kohchi; Hitoshi Iikura; Yasuaki Matsubara; Kohsuke Asoh; Takeshi Murata; Masami Kohchi; Eisaku Mizuguchi; Shinji Tsujii; Kazuo Hattori; Takaaki Miura; Yasushi Yoshimura; Satoshi Aida; Masanori Miwa; Ryoichi Saitoh; Naoaki Murao; Hisafumi Okabe; Charles Belunis; Cheryl Janson; Christine Lukacs; Verena Schück; Nobuo Shimma
Journal:  Bioorg Med Chem Lett       Date:  2011-01-21       Impact factor: 2.823

4.  Quantitative assessment of a change of hemosiderin deposition with age in splenic compartments of rats.

Authors:  T Masuda; R Satodate; K Tsuruga; T Kasai
Journal:  Tohoku J Exp Med       Date:  1993-07       Impact factor: 1.848

5.  MEK-ERK pathway modulation ameliorates disease phenotypes in a mouse model of Noonan syndrome associated with the Raf1(L613V) mutation.

Authors:  Xue Wu; Jeremy Simpson; Jenny H Hong; Kyoung-Han Kim; Nirusha K Thavarajah; Peter H Backx; Benjamin G Neel; Toshiyuki Araki
Journal:  J Clin Invest       Date:  2011-02-21       Impact factor: 14.808

6.  Effects of mechanical stress and carvedilol in lamin A/C-deficient dilated cardiomyopathy.

Authors:  Suchitra Chandar; Li Sze Yeo; Christiana Leimena; Ju-Chiat Tan; Xiao-Hui Xiao; Vesna Nikolova-Krstevski; Yoshinori Yasuoka; Margaret Gardiner-Garden; Jianxin Wu; Scott Kesteven; Lina Karlsdotter; Shweta Natarajan; Arthur Carlton; Stephen Rainer; Michael P Feneley; Diane Fatkin
Journal:  Circ Res       Date:  2009-12-17       Impact factor: 17.367

7.  Dual specificity phosphatase 4 mediates cardiomyopathy caused by lamin A/C (LMNA) gene mutation.

Authors:  Jason C Choi; Wei Wu; Antoine Muchir; Shinichi Iwata; Shunichi Homma; Howard J Worman
Journal:  J Biol Chem       Date:  2012-10-09       Impact factor: 5.157

8.  Heterozygous LmnadelK32 mice develop dilated cardiomyopathy through a combined pathomechanism of haploinsufficiency and peptide toxicity.

Authors:  Marie-Elodie Cattin; Anne T Bertrand; Saskia Schlossarek; Marie-Catherine Le Bihan; Søren Skov Jensen; Christiane Neuber; Claudia Crocini; Sophia Maron; Jeanne Lainé; Nathalie Mougenot; Shaïda Varnous; Yves Fromes; Arne Hansen; Thomas Eschenhagen; Valérie Decostre; Lucie Carrier; Gisèle Bonne
Journal:  Hum Mol Genet       Date:  2013-04-10       Impact factor: 6.150

9.  Mouse model carrying H222P-Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies.

Authors:  Takuro Arimura; Anne Helbling-Leclerc; Catherine Massart; Shaida Varnous; Florence Niel; Emmanuelle Lacène; Yves Fromes; Marcel Toussaint; Anne-Marie Mura; Dagmar I Keller; Helge Amthor; Richard Isnard; Marie Malissen; Ketty Schwartz; Gisèle Bonne
Journal:  Hum Mol Genet       Date:  2004-11-17       Impact factor: 6.150

10.  Real-time PCR based on SYBR-Green I fluorescence: an alternative to the TaqMan assay for a relative quantification of gene rearrangements, gene amplifications and micro gene deletions.

Authors:  Frederique Ponchel; Carmel Toomes; Kieran Bransfield; Fong T Leong; Susan H Douglas; Sarah L Field; Sandra M Bell; Valerie Combaret; Alain Puisieux; Alan J Mighell; Philip A Robinson; Chris F Inglehearn; John D Isaacs; Alex F Markham
Journal:  BMC Biotechnol       Date:  2003-10-13       Impact factor: 2.563

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  11 in total

1.  Cofilin-1 phosphorylation catalyzed by ERK1/2 alters cardiac actin dynamics in dilated cardiomyopathy caused by lamin A/C gene mutation.

Authors:  Maria Chatzifrangkeskou; David Yadin; Thibaut Marais; Solenne Chardonnet; Mathilde Cohen-Tannoudji; Nathalie Mougenot; Alain Schmitt; Silvia Crasto; Elisa Di Pasquale; Coline Macquart; Yannick Tanguy; Imen Jebeniani; Michel Pucéat; Blanca Morales Rodriguez; Wolfgang H Goldmann; Matteo Dal Ferro; Maria-Grazia Biferi; Petra Knaus; Gisèle Bonne; Howard J Worman; Antoine Muchir
Journal:  Hum Mol Genet       Date:  2018-09-01       Impact factor: 6.150

Review 2.  Extracellular signal-regulated kinases 1 and 2 regulate neuromuscular junction and myofiber phenotypes in mammalian skeletal muscle.

Authors:  Mendell Rimer
Journal:  Neurosci Lett       Date:  2019-12-02       Impact factor: 3.046

3.  Elevated dual specificity protein phosphatase 4 in cardiomyopathy caused by lamin A/C gene mutation is primarily ERK1/2-dependent and its depletion improves cardiac function and survival.

Authors:  Jason C Choi; Wei Wu; Elizabeth Phillips; Robin Plevin; Fusako Sera; Shunichi Homma; Howard J Worman
Journal:  Hum Mol Genet       Date:  2018-07-01       Impact factor: 6.150

Review 4.  Lamins and Lamin-Associated Proteins in Gastrointestinal Health and Disease.

Authors:  Graham F Brady; Raymond Kwan; Juliana Bragazzi Cunha; Jared S Elenbaas; M Bishr Omary
Journal:  Gastroenterology       Date:  2018-03-13       Impact factor: 22.682

Review 5.  Cell signaling abnormalities in cardiomyopathy caused by lamin A/C gene mutations.

Authors:  Howard J Worman
Journal:  Biochem Soc Trans       Date:  2017-12-01       Impact factor: 5.407

6.  Role of Cdkn2a in the Emery-Dreifuss Muscular Dystrophy Cardiac Phenotype.

Authors:  Gloria Pegoli; Marika Milan; Pierluigi Giuseppe Manti; Andrea Bianchi; Federica Lucini; Philina Santarelli; Claudia Bearzi; Roberto Rizzi; Chiara Lanzuolo
Journal:  Biomolecules       Date:  2021-04-06

Review 7.  The Pathogenesis and Therapies of Striated Muscle Laminopathies.

Authors:  Astrid Brull; Blanca Morales Rodriguez; Gisèle Bonne; Antoine Muchir; Anne T Bertrand
Journal:  Front Physiol       Date:  2018-10-30       Impact factor: 4.566

Review 8.  Cardiolaminopathies from bench to bedside: challenges in clinical decision-making with focus on arrhythmia-related outcomes.

Authors:  Giuseppe Boriani; Elena Biagini; Matteo Ziacchi; Vincenzo Livio Malavasi; Marco Vitolo; Marisa Talarico; Erminio Mauro; Giulia Gorlato; Giovanna Lattanzi
Journal:  Nucleus       Date:  2018       Impact factor: 4.197

9.  Ryanodine receptor remodeling in cardiomyopathy and muscular dystrophy caused by lamin A/C gene mutation.

Authors:  Haikel Dridi; Wei Wu; Steven R Reiken; Rachel M Ofer; Yang Liu; Qi Yuan; Leah Sittenfeld; Jared Kushner; Antoine Muchir; Howard J Worman; Andrew R Marks
Journal:  Hum Mol Genet       Date:  2021-02-25       Impact factor: 6.150

Review 10.  Mechanotransduction, nuclear architecture and epigenetics in Emery Dreifuss Muscular Dystrophy: tous pour un, un pour tous.

Authors:  Andrea Bianchi; Pierluigi Giuseppe Manti; Federica Lucini; Chiara Lanzuolo
Journal:  Nucleus       Date:  2018-01-01       Impact factor: 4.197

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