Polycystic kidney disease and therapeutic approaches

被引:18
作者
Park, Eun Young [1 ]
Woo, Yu Mi [1 ]
Park, Jong Hoon [1 ]
机构
[1] Sookmyung Womens Univ, Dept Biol Sci, Seoul 140742, South Korea
基金
新加坡国家研究基金会;
关键词
Drug development; Epigenetic; HDAC inhibitor; miRNA; Polycystic kidney disease; HISTONE DEACETYLASE INHIBITORS; EPITHELIAL-MESENCHYMAL TRANSITION; TUMOR-NECROSIS-FACTOR; RENAL CYST FORMATION; IN-VIVO; SIGNALING PATHWAYS; CELL-CYCLE; MICRORNA BIOGENESIS; SYSTEMS BIOLOGY; MIR-200; FAMILY;
D O I
10.5483/BMBRep.2011.44.6.359
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polycystic kidney disease (PKD) is a common genetic disorder in which extensive epithelial-lined cysts develop in the kidneys. In previous studies, abnormalities of polycystin protein and its interacting proteins, as well as primary cilia, have been suggested to play critical roles in the development of renal cysts. However, although several therapeutic targets for PKD have been suggested, no early diagnosis or effective treatments are currently available. Current developments are active for treatment of PKD including inhibitors or antagonists of PPAR-gamma, TNF-alpha, CDK and VEGF. These drugs are potential therapeutic targets in PKD, and need to be determined about pathological functions in human PKD. It has recently been reported that the alteration of epigenetic regulation, as well as gene mutations, may affect the pathogenesis of PKD. In this review, we will discuss recent approaches to PKD therapy. It provides important information regarding potential targets for PKD. [BMB reports 2011; 44(6): 359-368]
引用
收藏
页码:359 / 368
页数:10
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