Pharmacological Targeting of CDK9 in Cardiac Hypertrophy

被引:42
作者
Krystof, Vladimir [1 ,2 ]
Chamrad, Ivo [1 ,2 ,3 ]
Jorda, Radek [1 ,2 ]
Kohoutek, Jiri [4 ]
机构
[1] Palacky Univ, Lab Growth Regulators, Fac Sci, Olomouc 78371, Czech Republic
[2] Inst Expt Bot AS CR, Olomouc 78371, Czech Republic
[3] Palacky Univ, Fac Sci, Dept Biochem, Olomouc 78371, Czech Republic
[4] Vet Res Inst, Brno 62100, Czech Republic
关键词
P-TEFb; cardiac myocyte; cardiac hypertrophy; protein kinase; inhibitor; DEPENDENT KINASE INHIBITOR; P-TEFB COMPLEX; SPONGE KIRKPATRICKIA-VARIALOSA; CHINESE ANTILEUKEMIA MEDICINE; MUSCLE-CELL PROLIFERATION; ELONGATION-FACTOR-B; RNA-POLYMERASE; IN-VITRO; TRANSCRIPTION-ELONGATION; CRYSTAL-STRUCTURE;
D O I
10.1002/med.20172
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cardiac hypertrophy allows the heart to adapt to workload. hut persistent or unphysiological stimulus can result in pump failure Cardiac hypertrophy is characterized by an increase in the size of differentiated cardiac myocytes At the molecular level, growth (picas is linked to intensive transcription and translation Several cyclin-dependent kinases (CDKs) have been identified as principal regulators of transcription, and among these CDK9 is directly associated with cardiac hypertrophy CDK9 phosphorylates the C-terminal domain of RNA polymerase II and thus stimulates the elongation phase of transcription Chronic activation of CDK9 causes not only cardiac myocyte enlargement but also confers predisposition to heart failure Due to the long interest of molecular oncologists and medicinal chemists in CDKs as potential targets of anticancer drugs, a portfolio of small-molecule inhibitors of CDK9 is available Recent determination of CDK9's crystal structure now allows the development of selective inhibitors and their further optimization in terms of biochemical potency and selectivity CDK9 may therefore constitute a novel target for drugs against cardiac hypertrophy (c) 2009 Wiley Periodicals lire Med Res Rev. 30 No 4, 646-666 2010
引用
收藏
页码:646 / 666
页数:21
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