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US 2003/0148296 A1Published application
Differential gene expression in cardiac hypertrophy
OwnerHarlan Roger Brown, Traci Ann Mansfieldinventors
Life of this patent
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Abstract
Gene expression in normal unexercised hearts; chronically exercised, minimimally hypertrophied hearts; and hearts with hypertrophy due to renovascular hypertension is described. Methods of screening compounds for potential hypertrophic effects on cardiac muscle are provided.
Claims7
A method of screening a compound for effects on cardiac muscle, comprising:
- (a) administering a test compound to a test animal;
- (b) obtaining a sample of heart tissue from said animal;
- and
- (c) determining the level of expression of a gene selected from the group consisting of uncoupling protein 1 (UCP1), cytosolic malic enzyme, and atrial natriuretic factor (ANP);
- where increased expression of said gene in the test animal, compared to expression that would occur in a control animal, indicates said compound induces cardiac hypertrophy.
2 more elements
A method of screening a compound for effects on cardiac muscle, comprising:
- (a) administering a test compound to a test animal;
- (b) obtaining a sample of heart tissue from said animal;
- and
- (c) determining the level of expression of a gene selected from the group consisting of cofilin, cyclin-dependent kinase inhibitor p27 (p27kip1), smooth muscle 20 (SM-20), alpha cardiac myosin heavy chain (MYH6), mitochondrial long-chain 3-ketoacyl-CoA thiolase, medium chain acyl-CoA dehydrogenase, sarco/endoplasmic reticulum Ca2+ATPase (SERCA-2), and cyclin G;
- where decreased expression of said gene in the test animal, compared to expression that would occur in a control animal, indicates said compound induces cardiac hypertrophy.
2 more elements
A method of diagnosing cardiac hypertrophy in an animal, comprising:
- (a) obtaining a sample of heart tissue from said animal;
- and
- (b) determining at least one of the following:
- (i) whether the level of expression of a gene selected from the group consisting of cofilin, cyclin-dependent kinase inhibitor p27 (p27kip1), smooth muscle 20 (SM-20), alpha cardiac myosin heavy chain (MYH6), mitochondrial long-chain 3-ketoacyl-CoA thiolase, medium chain acyl-CoA dehydrogenase, sarco/endoplasmic reticulum Ca2+ATPase (SERCA-2), and cyclin G is decreased compared to normal levels of expression;
- (ii) whether the level of expression of a gene selected from the group consisting of uncoupling protein 1 (UCP1), cytosolic malic enzyme, and atrial natriuretic factor (ANP) is increased compared to normal levels of expression;
- (iii) whether the level of expression of a gene selected from the group consisting of nerve growth factor-induced-B (NGFI-B), D-binding protein, Thyrotroph Embryonic Factor (TEF), beta beta enolase, nocturnin, and deubiquitinating enzyme (UBP45) is increased compared to normal levels of expression;
- where increased expression of a gene of (I) or decreased expression of a gene of (ii) indicate that the hypertrophy is pathologic, and increased expression of a gene of (iii) indicate that the hypertrophy is physiologic.
4 more elements
Dependencies are inferred from the claim text.