Literature DB >> 26739211

Clinical impact of myocardial mTORC1 activation in nonischemic dilated cardiomyopathy.

Toshiyuki Yano1, Shinya Shimoshige1, Takayuki Miki1, Masaya Tanno1, Atsushi Mochizuki1, Takefumi Fujito1, Satoshi Yuda2, Atsuko Muranaka1, Makoto Ogasawara1, Akiyoshi Hashimoto3, Kazufumi Tsuchihashi3, Tetsuji Miura4.   

Abstract

BACKGROUND: Activity of mTOR complex 1 (mTORC1) has been shown to be up-regulated in animal models of heart failure. Here, we investigated the change and role of mTORC1 in human nonischemic dilated cardiomyopathy (NICM).
METHODS: Endomyocardial biopsy specimens were obtained from patients with NICM (n=52) and from Brugada syndrome patients with normal LVEF as controls (n=10). The specimens were stained for phospho-ribosomal protein S6 (p-Rps6) and phospho-p70S6K (p-p70S6K), and the area with p-Rps6 signal was used as an index of mTORC1 activity. Using median mTORC1 activity, patients were divided into a high mTORC1 activity (H-mTOR) group and a low mTORC1 activity (L-mTOR) group.
RESULTS: The ratio of p-Rps6-positive area in biopsy samples was 10-fold larger in patients with NICM than in controls (2.0±2.2% vs. 0.2±0.2%, p<0.01). p-p70S6K signal level was higher in the H-mTOR group than in the L-mTOR group. The proportion of patients with a family history of cardiomyopathy was higher and the proportion of patients on ACE inhibitors or angiotensin receptor blockers was lower in the H-mTOR group than in the L-mTOR group. The p-Rps6-positive area was correlated with extent of myocardial fibrosis (r=0.46, p<0.01). The cardiac event-free survival rate during a 5-year follow-up period tended to be lower in the H-mTOR group than in the L-mTOR group (52.9% vs. 81.6%, P=0.10).
CONCLUSION: Aberrant activation of mTORC1 in cardiomyocytes was associated with myocardial fibrosis and a trend for worse prognosis in patients with NICM, indicating that persistently activated mTORC1 contributes to progression of human heart failure.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Angiotensin; Dilated cardiomyopathy; Endomyocardial biopsy; Heart failure; Ribosomal protein S6; mTOR

Mesh:

Substances:

Year:  2015        PMID: 26739211     DOI: 10.1016/j.yjmcc.2015.12.022

Source DB:  PubMed          Journal:  J Mol Cell Cardiol        ISSN: 0022-2828            Impact factor:   5.000


  12 in total

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Review 2.  Role of titin in cardiomyopathy: from DNA variants to patient stratification.

Authors:  James S Ware; Stuart A Cook
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3.  De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathy.

Authors:  Michael T Zimmermann; Maengjo Kim; Pamela A Long; Jared M Evans; Xiaolei Xu; Timothy M Olson
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Review 4.  Oncometabolic Tracks in the Heart.

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6.  Titin-truncating variants affect heart function in disease cohorts and the general population.

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Review 7.  Therapeutic Potential of Oxytocin in Atherosclerotic Cardiovascular Disease: Mechanisms and Signaling Pathways.

Authors:  Ping Wang; Stephani C Wang; Haipeng Yang; Chunmei Lv; Shuwei Jia; Xiaoyu Liu; Xiaoran Wang; Dexin Meng; Danian Qin; Hui Zhu; Yu-Feng Wang
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Journal:  Nat Chem Biol       Date:  2019-07-08       Impact factor: 15.040

Review 9.  The Giant Protein Titin's Role in Cardiomyopathy: Genetic, Transcriptional, and Post-translational Modifications of TTN and Their Contribution to Cardiac Disease.

Authors:  Charles A Tharp; Mary E Haywood; Orfeo Sbaizero; Matthew R G Taylor; Luisa Mestroni
Journal:  Front Physiol       Date:  2019-11-28       Impact factor: 4.566

10.  Molecular, Cellular, and Clinical Evidence That Sodium-Glucose Cotransporter 2 Inhibitors Act as Neurohormonal Antagonists When Used for the Treatment of Chronic Heart Failure.

Authors:  Milton Packer
Journal:  J Am Heart Assoc       Date:  2020-08-01       Impact factor: 5.501

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