Wang Songyan, Li Bing, Li Chunguang, Cui Wenpeng, Miao Lining
Department of Nephrology, Second Hospital of Jilin University, Changchun 130041, China ; Department of Nephrology, Jilin Province People's Hospital, Changchun 130021, China.
Department of Nephrology, Jilin Province People's Hospital, Changchun 130021, China.
J Diabetes Res. 2015;2015:962383. doi: 10.1155/2015/962383. Epub 2015 Sep 2.
Diabetic nephropathy (DN) is the leading cause of end-stage renal disease (ESRD). The development and progression of DN might involve multiple factors. Connective tissue growth factor (CCN2, originally known as CTGF) is the one which plays a pivotal role. Therefore, increasing attention is being paid to CCN2 as a potential therapeutic target for DN. Up to date, there are also many drugs or agents which have been shown for their protective effects against DN via different mechanisms. In this review, we only focus on the potential renoprotective therapeutic agents which can specifically abolish CCN2 expression or nonspecifically inhibit CCN2 expression for retarding the development and progression of DN.
糖尿病肾病(DN)是终末期肾病(ESRD)的主要病因。DN的发生和发展可能涉及多种因素。结缔组织生长因子(CCN2,最初称为CTGF)在其中起着关键作用。因此,CCN2作为DN的潜在治疗靶点正受到越来越多的关注。迄今为止,也有许多药物或制剂已被证明可通过不同机制对DN具有保护作用。在本综述中,我们仅关注能够特异性消除CCN2表达或非特异性抑制CCN2表达以延缓DN发生和发展的潜在肾脏保护治疗药物。