Expression of microRNA-208 is Associated With Adverse Clinical Outcomes in Human Dilated Cardiomyopathy

Journal of Cardiac Failure

Volumn 16, Issue 5, 2010, Pages 404-410

  Satoh, Mamoru ^a   Minami, Yoshitaka ^a   Takahashi, Yuji ^a   Tabuchi, Tsuyoshi ^a   Nakamura, Motoyuki ^a  

^a Department of Internal Medicine   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN; MICRORNA; MICRORNA 208; MICRORNA 208B; MICRORNA 499; MYOSIN HEAVY CHAIN ALPHA; MYOSIN HEAVY CHAIN BETA; RNA; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CONGESTIVE CARDIOMYOPATHY; CONTROLLED STUDY; DISEASE COURSE; FEMALE; GENE EXPRESSION; HEART LEFT VENTRICLE FUNCTION; HEART MUSCLE BIOPSY; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; OUTCOME ASSESSMENT; PRIORITY JOURNAL; PROGNOSIS;

CARDIOMYOPATHY, DILATED; CASE-CONTROL STUDIES; COLLAGEN; CONFIDENCE INTERVALS; DISEASE PROGRESSION; FEMALE; HUMANS; JAPAN; LOGISTIC MODELS; MALE; MICRORNAS; MIDDLE AGED; MULTIVARIATE ANALYSIS; MYOSIN HEAVY CHAINS; PROGNOSIS; RISK; RISK FACTORS; STATISTICS AS TOPIC; STROKE VOLUME; TREATMENT OUTCOME; VENTRICULAR FUNCTION, LEFT; VENTRICULAR MYOSINS;

EID: 77951627045     PISSN: 10719164     EISSN: 15328414     Source Type: Journal    
DOI: 10.1016/j.cardfail.2010.01.002     Document Type: Article

References (28)

1. Nadal-Ginard B., and Mahdavi V. Molecular basis of cardiac performance. Plasticity of the myocardium generated through protein isoform switches. J Clin Invest 84 (1989) 1693-1700
2. Pope B., Hoh J.F., and Weeds A. The ATPase activities of rat cardiac myosin isoenzymes. FEBS Lett 118 (1980) 205-208
3. Bouvagnet P., Mairhofer H., Leger J.O., Puech P., and Leger J.J. Distribution pattern of alpha and beta myosin in normal and diseased human ventricular myocardium. Basic Res Cardiol 84 (1989) 91-102
4. Nakao K., Minobe W., Roden R., Bristow M.R., and Leinwand L.A. Myosin heavy chain gene expression in human heart failure. J Clin Invest 100 (1997) 2362-2370
5. Abraham W.T., Gilbert E.M., Lowes B.D., Minobe W.A., Larrabee P., Roden R.L., et al. Coordinate changes in myosin heavy chain isoform gene expression are selectively associated with alterations in dilated cardiomyopathy phenotype. Mol Med 8 (2002) 750-760
6. Bartel D.P. MicroRNAs: genomics, biogenesis, mechanism, and function. Cell 116 (2004) 281-297
7. Kim V.N. Small RNAs: classification, biogenesis, and function. Mol Cells 19 (2005) 1-15
8. Petersen C.P., Bordeleau M.E., Pelletier J., and Sharp P.A. Short RNAs repress translation after initiation in mammalian cells. Mol Cells 21 (2006) 533-542
9. Van Rooij E., Sutherland L.B., Qi X., Richardson J.A., Hill J., and Olson E.N. Control of stress-dependent cardiac growth and gene expression by a microRNA. Science 316 (2007) 575-579
10. van Rooij E., Quiat D., Johnson B.A., Sutherland L.B., Qi X., Richardson J.A., et al. A family of microRNAs encoded by myosin genes governs myosin expression and muscle performance. Dev Cell 17 (2009) 662-673
11. Richardson P., McKenna W., Bristow M., Maisch B., Mautner B., O'Connell J., et al. Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies. Circulation 93 (1996) 841-842
12. Schmittgen T.D., Lee E.J., Jiang J., Sarkar A., Yang L., Elton T.S., et al. Real-time PCR quantification of precursor and mature microRNA. Methods 44 (2008) 31-38
13. Livak K.J., and Schmittgen T.D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods 25 (2001) 402-408
14. Miyata S., Minobe W., Bristow M.R., and Leinwand L.A. Myosin heavy chain isoform expression in the failing and nonfailing human heart. Circ Res 86 (2000) 386-390
15. Krenz M., and Robbins J. Impact of beta-myosin heavy chain expression on cardiac function during stress. J Am Coll Cardiol 44 (2004) 2390-2397
16. Alpert N.R., and Mulieri L.A. Increased myothermal economy of isometric force generation in compensated cardiac hypertrophy induced by pulmonary artery constriction in the rabbit. A characterization of heat liberation in normal and hypertrophied right ventricular papillary muscles. Circ Res 50 (1982) 491-500
17. Holubarsch C., Goulette R.P., Litten R.Z., Martin B.J., Mulieri L.A., and Alpert N.R. The economy of isometric force development, myosin isoenzyme pattern and myofibrillar ATPase activity in normal and hypothyroid rat myocardium. Circ Res 56 (1985) 78-86
18. Cheng Y., Ji R., Yue J., Yang J., Liu X., Chen H., et al. MicroRNAs are aberrantly expressed in hypertrophic heart: do they play a role in cardiac hypertrophy?. Am J Pathol 170 (2007) 1831-1840
19. Carè A., Catalucci D., Felicetti F., Bonci D., Addario A., Gallo P., et al. MicroRNA-133 controls cardiac hypertrophy. Nat Med 13 (2007) 613-618
20. Van Rooij E., Sutherland L.B., Liu N., Williams A.H., McAnally J., Gerard R.D., et al. A signature pattern of stress-responsive microRNAs that can evoke cardiac hypertrophy and heart failure. Proc Natl Acad Sci USA 103 (2006) 18255-18260
21. Ambros V., Lee R.C., Lavanway A., Williams P.T., and Jewell D. MicroRNAs and other tiny endogenous RNAs in C. elegans. Curr Biol 13 (2003) 807-818
22. Reiser P.J., and Kline W.O. Electrophoretic separation and quantitation of cardiac myosin heavy chain isoforms in eight mammalian species. Am J Physiol 274 (1998) H1048-H1053
23. Chien K.R. Genomic circuits and the integrative biology of cardiac diseases. Nature 407 (2000) 227-2
24. Callis T.E., Pandya K., Seok H.Y., Tang R.H., Tatsuguchi M., Huang Z.P., et al. MicroRNA-208a is a regulator of cardiac hypertrophy and conduction in mice. J Clin Invest 119 (2009) 2772-2786
25. Pandya K., Kim H.S., and Smithies O. Fibrosis, not cell size, delineates beta-myosin heavy chain reexpression during cardiac hypertrophy and normal aging in vivo. Proc Natl Acad Sci USA 103 (2006) 16864-16869
26. Lowes B.D., Minobe W., Abraham W.T., Rizeq M.N., Bohlmeyer T.J., Quaife R.A., et al. Changes in gene expression in the intact human heart. Downregulation of alpha-myosin heavy chain in hypertrophied, failing ventricular myocardium. J Clin Invest 100 (1997) 2315-2324
27. Chen J.F., Mandel E.M., Thomson J.M., Wu Q., Callis T.E., Hammond S.M., et al. The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation. Nat Genet 38 (2006) 228-233
28. Liu N., Williams A.H., Kim Y., McAnally J., Bezprozvannaya S., Sutherland L.B., et al. An intragenic MEF2-dependent enhancer directs muscle-specific expression of microRNAs 1 and 133. Proc Natl Acad Sci USA 104 (2007) 20844-20849