TY - JOUR
T1 - Chronic heart failure
T2 - Ca2+, catabolism, and catastrophic cell death
AU - Cho, Geoffrey W.
AU - Altamirano, Francisco
AU - Hill, Joseph A.
N1 - Funding Information:
This work was supported by grants from the NIH ( HL-120732 ; HL-100401 ), AHA ( 14SFRN20510023 ; 14SFRN20670003 ), Fondation Leducq ( 11CVD04 ) and CPRIT ( RP110486P3 ).
Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2016/4/1
Y1 - 2016/4/1
N2 - Robust successes have been achieved in recent years in conquering the acutely lethal manifestations of heart disease. Many patients who previously would have died now survive to enjoy happy and productive lives. Nevertheless, the devastating impact of heart disease continues unabated, as the spectrum of disease has evolved with new manifestations. In light of this ever-evolving challenge, insights that culminate in novel therapeutic targets are urgently needed. Here, we review fundamental mechanisms of heart failure, both with reduced (HFrEF) and preserved (HFpEF) ejection fraction. We discuss pathways that regulate cardiomyocyte remodeling and turnover, focusing on Ca2+ signaling, autophagy, and apoptosis. In particular, we highlight recent insights pointing to novel connections among these events. We also explore mechanisms whereby potential therapeutic approaches targeting these processes may improve morbidity and mortality in the devastating syndrome of heart failure.
AB - Robust successes have been achieved in recent years in conquering the acutely lethal manifestations of heart disease. Many patients who previously would have died now survive to enjoy happy and productive lives. Nevertheless, the devastating impact of heart disease continues unabated, as the spectrum of disease has evolved with new manifestations. In light of this ever-evolving challenge, insights that culminate in novel therapeutic targets are urgently needed. Here, we review fundamental mechanisms of heart failure, both with reduced (HFrEF) and preserved (HFpEF) ejection fraction. We discuss pathways that regulate cardiomyocyte remodeling and turnover, focusing on Ca2+ signaling, autophagy, and apoptosis. In particular, we highlight recent insights pointing to novel connections among these events. We also explore mechanisms whereby potential therapeutic approaches targeting these processes may improve morbidity and mortality in the devastating syndrome of heart failure.
KW - Apoptosis
KW - Autophagy
KW - Calcium homeostasis
KW - Heart failure
KW - Remodeling
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U2 - 10.1016/j.bbadis.2016.01.011
DO - 10.1016/j.bbadis.2016.01.011
M3 - Review article
AN - SCOPUS:84958817706
VL - 1862
SP - 763
EP - 777
JO - Biochimica et Biophysica Acta - Molecular Basis of Disease
JF - Biochimica et Biophysica Acta - Molecular Basis of Disease
SN - 0925-4439
IS - 4
ER -