Protein kinase D and keratinocyte proliferation

被引:30
作者
Bollag, WB
Dodd, ME
Shapiro, BA
机构
[1] Med Coll Georgia, IMMAG, Augusta, GA 30912 USA
[2] Med Coll Georgia, Dept Med Dermatol, Augusta, GA 30912 USA
[3] Med Coll Georgia, Dept Cell Biol & Anat, Augusta, GA 30912 USA
关键词
D O I
10.1358/dnp.2004.17.2.829045
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Keratinocytes undergo a distinct pattern of proliferation and differentiation that is essential for the function of the skin as a protective barrier. Defects in the equilibrium between proliferation and differentiation compromise the skin's barrier function and give rise to human diseases such as psoriasis and nonmelanoma skin cancer. The identification of protein kinase C (PKC) as a major cellular target for tumor-promoting phorbol esters suggested the involvement of this enzyme in the regulation of keratinocyte proliferation and tumorigenesis; however, results have demonstrated the existence in keratinocytes and other cell types of another diacylglycerol/phorbol ester-responsive protein kinase: protein kinase D (PKD) in mouse, also known as PKCmu in humans. Although numerous data suggest the importance of PKD/PKCmu in processes related to proliferation in many cell types, including keratinocytes, there are no specific inhibitors of PKD currently available. Current treatment strategies for hyperproliferative skin disorders are often suboptimal, either because of lack of efficacy or because of contraindications due to deleterious side effects or aesthetic considerations. Thus, PKD/PKCmu may represent a novel target for the development of new and more efficacious drug treatments for hyperproliferative skin disorders. C 2004 Prous Science. All rights reserved.
引用
收藏
页码:117 / 126
页数:10
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