TY - JOUR
T1 - Small-molecule therapies for cardiac hypertrophy
T2 - Moving beneath the cell surface
AU - McKinsey, Timothy A.
AU - Kass, David A.
N1 - Funding Information:
T.A.M. thanks E. Bush for helpful discussions and L. Castonguay for assistance with the compound structures. D.A.K. is supported by NIH-PO1-HL-077180 and PO1-HL-59408 grants, and the Peter Belfer Laboratory Research Fund.
Copyright:
Copyright 2009 Elsevier B.V., All rights reserved.
PY - 2007/8
Y1 - 2007/8
N2 - Pathological stress from cardiovascular disease stimulates hypertrophy of heart cells, which increases the risk of cardiac morbidity and mortality. Recent evidence has indicated that inhibiting such hypertrophy could be beneficial, encouraging drug discovery and development efforts for agents that could achieve this goal. Most existing therapies that have antihypertrophic effects target outside-in signalling in cardiac cells, but their effectiveness seems limited, and so attention has recently turned to the potential of targeting intracellular signalling pathways. Here, we focus on new developments with small-molecule inhibitors of cardiac hypertrophy, summarizing both agents that have been in or are poised for clinical testing, and pathways that offer further promising potential therapeutic targets.
AB - Pathological stress from cardiovascular disease stimulates hypertrophy of heart cells, which increases the risk of cardiac morbidity and mortality. Recent evidence has indicated that inhibiting such hypertrophy could be beneficial, encouraging drug discovery and development efforts for agents that could achieve this goal. Most existing therapies that have antihypertrophic effects target outside-in signalling in cardiac cells, but their effectiveness seems limited, and so attention has recently turned to the potential of targeting intracellular signalling pathways. Here, we focus on new developments with small-molecule inhibitors of cardiac hypertrophy, summarizing both agents that have been in or are poised for clinical testing, and pathways that offer further promising potential therapeutic targets.
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U2 - 10.1038/nrd2193
DO - 10.1038/nrd2193
M3 - Review article
C2 - 17643091
AN - SCOPUS:34547665415
SN - 1474-1776
VL - 6
SP - 617
EP - 635
JO - Nature Reviews Drug Discovery
JF - Nature Reviews Drug Discovery
IS - 8
ER -