Protein kinase C inhibitors: a patent review (2010-present)

被引:7
作者
Sobhia, Masilamani Elizabeth [1 ]
Grewal, Baljinder K. [1 ]
Paul, Matam Losery Stanly [1 ]
Patel, Jigneshkumar [1 ]
Kaur, Amandeep [1 ]
Haokip, Thongtinlal [1 ]
Kokkula, Alekhya [1 ]
机构
[1] Natl Inst Pharmaceut Educ & Res, Dept Pharmacoinformat, SAS Nagar Mohali, Punjab, India
关键词
activation; diseases; patents; PKCs; CARDIOVASCULAR COMPLICATIONS; ACTIVATION; PKC; BETA; ALPHA; ISOFORM; DISEASE; CELLS; EXPRESSION; DEFICIENT;
D O I
10.1517/13543776.2013.812073
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Introduction: Protein kinase C (PKC) comprises at least 10 isoforms, pivotal in various cellular differentiation processes and in other specific cellular functions. Catalytic subunits of all PKCs are highly conserved which play a central role in the development of kinase-specific inhibitors for the treatment of a number of diseases and also in the drug resistance and immunological disorders. The authors' previous work of reviewing patents of PKC inhibitors is continued in this report. Area covered: Thorough survey on the physiological roles of PKC isoforms and patents filed for PKC inhibitors from 2010 to present representing new and potential strategy for the cure and prevention of disorders due to elevation in various PKC levels is reported. Expert opinion: The PKC isoforms are unique in terms of tissue distribution and an elevation in any isoform level results in different diseased conditions. Different PKC isoforms have high sequence identity but they are involved in different diseases. Crystal structure of few PKC isoforms viz. C1 domain of PKC delta, the C2 domains of PKC alpha and beta, kinase domain and full structure of PKC beta II are known. Identification of more crystal structures and thorough analysis of available structures and information on the PKC ligands will be helpful in the drug designing and development processes.
引用
收藏
页码:1451 / 1468
页数:18
相关论文
共 89 条
[41]   Protein kinase C θ inhibits insulin signaling by phosphorylating IRS1 at Ser1101 [J].
Li, Y ;
Soos, TJ ;
Li, XH ;
Wu, J ;
DeGennaro, M ;
Sun, XJ ;
Littman, DR ;
Birnbaum, MJ ;
Polakiewicz, RD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (44) :45304-45307
[42]   Glucose-induced TGF-β1 and TGF-β receptor-1 expression in vascular smooth muscle cells is mediated by protein kinase C-α [J].
Lindschau, C ;
Quass, P ;
Menne, J ;
Güler, F ;
Fiebeler, A ;
Leitges, M ;
Luft, FC ;
Haller, H .
HYPERTENSION, 2003, 42 (03) :335-341
[43]   PKC-ε-dependent survival signals in diabetic hearts [J].
Malhotra, A ;
Begley, R ;
Kang, BPS ;
Rana, I ;
Liu, J ;
Yang, GP ;
Mochly-Rosen, D ;
Meggs, LG .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2005, 289 (04) :H1343-H1350
[44]   Classical PKC isoforms in cancer [J].
Martiny-Baron, Georg ;
Fabbro, Doriano .
PHARMACOLOGICAL RESEARCH, 2007, 55 (06) :477-486
[45]  
Masters CL, 2012, COLD SPRING HARB PER, V2, P1
[46]  
Meier M, 2000, VASC MED, V5, P173, DOI 10.1191/135886300701568405
[47]   Targeting the protein kinase C family in the diabetic kidney: lessons from analysis of mutant mice [J].
Meier, M. ;
Menne, J. ;
Haller, H. .
DIABETOLOGIA, 2009, 52 (05) :765-775
[48]   Dual Inhibition of Classical Protein Kinase C-α and Protein Kinase C-β Isoforms Protects Against Experimental Murine Diabetic Nephropathy [J].
Menne, Jan ;
Shushakova, Nelli ;
Bartels, Janina ;
Kiyan, Yulia ;
Laudeley, Robert ;
Haller, Hermann ;
Park, Joon-Keun ;
Meier, Matthias .
DIABETES, 2013, 62 (04) :1167-1174
[49]   Inhibition of degranulation and interleukin-6 production in mast cells derived from mice deficient in protein kinase Cβ [J].
Nechushtan, H ;
Leitges, M ;
Cohen, C ;
Kay, G ;
Razin, E .
BLOOD, 2000, 95 (05) :1752-1757
[50]  
NEWTON AC, 1995, J BIOL CHEM, V270, P28495, DOI 10.1074/jbc.270.48.28495