Histone deacetylase (HDAC) inhibitors attenuate cardiac hypertrophy by suppressing autophagy (Q24603793)

2

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Pavan K Battiprolu

3

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Nan Jiang

4

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Cyndi R Morales

5

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Yongli Kong

6

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Beverly A Rothermel

7

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Thomas G Gillette

8

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Joseph A Hill

Proceedings of the National Academy of Sciences of the United States of America

9

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language of work or name

English

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publication date

8 March 2011

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published in

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volume

108

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issue

10

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page(s)

4123-8

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cites work

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Hdac2 regulates the cardiac hypertrophic response by modulating Gsk3 beta activity

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7 April 2017

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Histone deacetylases 5 and 9 govern responsiveness of the heart to a subset of stress signals and play redundant roles in heart development

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Autophagy inhibition enhances therapy-induced apoptosis in a Myc-induced model of lymphoma

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The clinical development of histone deacetylase inhibitors as targeted anticancer drugs

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Autophagy in hypertensive heart disease

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FoxO transcription factors promote autophagy in cardiomyocytes

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27 September 2017

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Cardiac autophagy is a maladaptive response to hemodynamic stress

27 September 2017

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Targeting autophagy augments the anticancer activity of the histone deacetylase inhibitor SAHA to overcome Bcr-Abl-mediated drug resistance

27 September 2017

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Suppression of class I and II histone deacetylases blunts pressure-overload cardiac hypertrophy

27 September 2017

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27 September 2017

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Apoptotic and autophagic cell death induced by histone deacetylase inhibitors

27 September 2017

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Essential function of histone deacetylase 1 in proliferation control and CDK inhibitor repression

27 September 2017

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Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease).

27 September 2017

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Molecular pathways underlying cardiac remodeling during pathophysiological stimulation

27 September 2017

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Inhibition of histone deacetylation blocks cardiac hypertrophy induced by angiotensin II infusion and aortic banding

30 May 2018

1 reference

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Reduced body size and decreased intestinal tumor rates in HDAC2-mutant mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1015081108

Suppression of cardiomyocyte hypertrophy by inhibition of the ubiquitin-proteasome system

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1015081108

Proteasome inhibition promotes regression of left ventricular hypertrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1015081108

Autophagy is required to maintain muscle mass.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.1015081108

Cardiac hypertrophy is not a required compensatory response to short-term pressure overload

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21367693

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Activation of the cardiac proteasome during pressure overload promotes ventricular hypertrophy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21367693

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Histone deacetylase inhibition in the treatment of heart disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21367693

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.1015081108

1 reference

ADS bibcode

2011PNAS..108.4123C

0 references

1 reference

1 reference

PubMed publication ID

21367693

1 reference