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The nuclear and mitochondrial sirtuins, Sirt6 and Sirt3, regulate each other's activity and protect the heart from developing obesity‐mediated diabetic cardiomyopathy

The FASEB journal, 2019-10, Vol.33 (10), p.10872-10888

2019

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Honokiol blocks and reverses cardiac hypertrophy in mice by activating mitochondrial Sirt3

Nature communications, 2015-04, Vol.6 (1), p.6656-6656, Article 6656

2015

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SIRT3 Deacetylates and Activates OPA1 To Regulate Mitochondrial Dynamics during Stress

Molecular and Cellular Biology, 2014-03, Vol.34 (5), p.807-819

2014

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The sirtuin SIRT6 blocks IGF-Akt signaling and development of cardiac hypertrophy by targeting c-Jun

Nature medicine, 2012-11, Vol.18 (11), p.1643-1650

2012

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Sirt3 protects mitochondrial DNA damage and blocks the development of doxorubicin-induced cardiomyopathy in mice

American journal of physiology. Heart and circulatory physiology, 2016-04, Vol.310 (8), p.H962-H972

2016

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Exogenous NAD Blocks Cardiac Hypertrophic Response via Activation of the SIRT3-LKB1-AMP-activated Kinase Pathway

The Journal of biological chemistry, 2010-01, Vol.285 (5), p.3133-3144

2010

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Honokiol, an activator of Sirtuin-3 (SIRT3) preserves mitochondria and protects the heart from doxorubicin-induced cardiomyopathy in mice

Oncotarget, 2017-05, Vol.8 (21), p.34082-34098

2017

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SIRT3 Is a Stress-Responsive Deacetylase in Cardiomyocytes That Protects Cells from Stress-Mediated Cell Death by Deacetylation of Ku70

Molecular and Cellular Biology, 2008-10, Vol.28 (20), p.6384-6401

2008

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The deacetylase SIRT1 promotes membrane localization and activation of Akt and PDK1 during tumorigenesis and cardiac hypertrophy

Science signaling, 2011-07, Vol.4 (182), p.ra46

2011

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SIRT3 blocks myofibroblast differentiation and pulmonary fibrosis by preventing mitochondrial DNA damage

American journal of physiology. Lung cellular and molecular physiology, 2017-01, Vol.312 (1), p.L68-L78

2017

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SIRT1 Promotes Cell Survival under Stress by Deacetylation-Dependent Deactivation of Poly(ADP-Ribose) Polymerase 1

Molecular and Cellular Biology, 2009-08, Vol.29 (15), p.4116-4129

2009

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Emerging roles of SIRT1 deacetylase in regulating cardiomyocyte survival and hypertrophy

Journal of molecular and cellular cardiology, 2011-10, Vol.51 (4), p.614-618

2011

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Nampt secreted from cardiomyocytes promotes development of cardiac hypertrophy and adverse ventricular remodeling

American journal of physiology. Heart and circulatory physiology, 2013-02, Vol.304 (3), p.H415-H426

2013

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Regulation of Akt signaling by sirtuins: its implication in cardiac hypertrophy and aging

Circulation research, 2014-01, Vol.114 (2), p.368-378

2014

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Acetylation of a Conserved Lysine Residue in the ATP Binding Pocket of p38 Augments Its Kinase Activity during Hypertrophy of Cardiomyocytes

Molecular and Cellular Biology, 2011-06, Vol.31 (11), p.2349-2363

2011

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Role of Sirtuins in Regulating Pathophysiology of the Heart

Trends in endocrinology and metabolism, 2016-08, Vol.27 (8), p.563-573

2016

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Skeletal muscle‐specific over‐expression of the nuclear sirtuin SIRT6 blocks cancer‐associated cachexia by regulating multiple targets

JCSM rapid communications, 2021-01, Vol.4 (1), p.40-56

2021

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Is nuclear sirtuin SIRT6 a master regulator of immune function?

American journal of physiology: endocrinology and metabolism, 2021-03, Vol.320 (3), p.E399-E414

2021

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SIRT3 Blocks Aging-Associated Tissue Fibrosis in Mice by Deacetylating and Activating Glycogen Synthase Kinase 3β

Molecular and cellular biology, 2016-03, Vol.36 (5), p.678-692

2016

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The nuclear sirtuin SIRT6 protects the heart from developing aging-associated myocyte senescence and cardiac hypertrophy

Aging (Albany, NY.), 2021-05, Vol.13 (9), p.12334-12358

2021

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The histone deacetylase SIRT6 blocks myostatin expression and development of muscle atrophy

Scientific reports, 2017-09, Vol.7 (1), p.11877-18, Article 11877

2017

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Mitochondrial SIRT3 and heart disease

Cardiovascular research, 2010-11, Vol.88 (2), p.250-256

2010

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Histone Deacetylase 3 (HDAC3)-dependent Reversible Lysine Acetylation of Cardiac Myosin Heavy Chain Isoforms Modulates Their Enzymatic and Motor Activity

The Journal of biological chemistry, 2015-06, Vol.290 (25), p.15559-15569

2015

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HDAC3-dependent Reversible Lysine Acetylation of Cardiac Myosin Heavy Chain Isoforms Modulates Their Enzymatic and Motor Activity

The Journal of biological chemistry, 2011-02, Vol.286 (7), p.5567-5577

2011

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Activation of SIRT1, a class III histone deacetylase, contributes to fructose feeding-mediated induction of the alpha-myosin heavy chain expression

American journal of physiology. Heart and circulatory physiology, 2008-03, Vol.294 (3), p.H1388-H1397

2008

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The nuclear and mitochondrial sirtuins, Sirt6 and Sirt3, regulate each other's activity and protect the heart from developing obesity‐mediated diabetic cardiomyopathy

Honokiol blocks and reverses cardiac hypertrophy in mice by activating mitochondrial Sirt3

SIRT3 Deacetylates and Activates OPA1 To Regulate Mitochondrial Dynamics during Stress

The sirtuin SIRT6 blocks IGF-Akt signaling and development of cardiac hypertrophy by targeting c-Jun

Sirt3 protects mitochondrial DNA damage and blocks the development of doxorubicin-induced cardiomyopathy in mice

Exogenous NAD Blocks Cardiac Hypertrophic Response via Activation of the SIRT3-LKB1-AMP-activated Kinase Pathway

Honokiol, an activator of Sirtuin-3 (SIRT3) preserves mitochondria and protects the heart from doxorubicin-induced cardiomyopathy in mice

SIRT3 Is a Stress-Responsive Deacetylase in Cardiomyocytes That Protects Cells from Stress-Mediated Cell Death by Deacetylation of Ku70

The deacetylase SIRT1 promotes membrane localization and activation of Akt and PDK1 during tumorigenesis and cardiac hypertrophy

SIRT3 blocks myofibroblast differentiation and pulmonary fibrosis by preventing mitochondrial DNA damage

SIRT1 Promotes Cell Survival under Stress by Deacetylation-Dependent Deactivation of Poly(ADP-Ribose) Polymerase 1

Emerging roles of SIRT1 deacetylase in regulating cardiomyocyte survival and hypertrophy

Nampt secreted from cardiomyocytes promotes development of cardiac hypertrophy and adverse ventricular remodeling

Regulation of Akt signaling by sirtuins: its implication in cardiac hypertrophy and aging

Acetylation of a Conserved Lysine Residue in the ATP Binding Pocket of p38 Augments Its Kinase Activity during Hypertrophy of Cardiomyocytes

Role of Sirtuins in Regulating Pathophysiology of the Heart

Skeletal muscle‐specific over‐expression of the nuclear sirtuin SIRT6 blocks cancer‐associated cachexia by regulating multiple targets

Is nuclear sirtuin SIRT6 a master regulator of immune function?

SIRT3 Blocks Aging-Associated Tissue Fibrosis in Mice by Deacetylating and Activating Glycogen Synthase Kinase 3β

The nuclear sirtuin SIRT6 protects the heart from developing aging-associated myocyte senescence and cardiac hypertrophy

The histone deacetylase SIRT6 blocks myostatin expression and development of muscle atrophy

Mitochondrial SIRT3 and heart disease

Histone Deacetylase 3 (HDAC3)-dependent Reversible Lysine Acetylation of Cardiac Myosin Heavy Chain Isoforms Modulates Their Enzymatic and Motor Activity

HDAC3-dependent Reversible Lysine Acetylation of Cardiac Myosin Heavy Chain Isoforms Modulates Their Enzymatic and Motor Activity

Activation of SIRT1, a class III histone deacetylase, contributes to fructose feeding-mediated induction of the alpha-myosin heavy chain expression

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