Nelson Peter J, Shankland Stuart J
Division of Nephrology, New York University School of Medicine, New York, NY 10016, USA.
Nephron Exp Nephrol. 2006;103(1):e6-15. doi: 10.1159/000090138. Epub 2005 Dec 7.
Discovery into the molecular basis of renal disease is occurring at an unprecedented rate. With the advent of the NIH Roadmap, there is a greater expectation of translating this knowledge into new treatments. Here, we review the therapeutic strategy to preserve renal function in proliferative renal diseases by directly inhibiting the mitogenic pathways within renal parenchymal cells that promote G0 to G1/S cell-cycle phase progression. Reductionist methodologies have identified several antiproliferative molecular targets, and promising preclinical testing of leading small-molecule drugs to modulate these targets has now led to landmark clinical trials. Yet, this advancement into targeted therapy highlights important differences between the therapeutic goals of molecular nephrology versus molecular oncology and, by extension, the poorly understood role of alternative target activity in drug efficacy. Systems research to clarify these issues should accelerate the development of this promising therapeutic strategy.
对肾脏疾病分子基础的发现正以前所未有的速度进行着。随着美国国立卫生研究院路线图的出现,人们对将这些知识转化为新疗法抱有更高期望。在此,我们回顾通过直接抑制肾实质细胞内促进G0期到G1/S期细胞周期进展的有丝分裂途径来保护增殖性肾脏疾病肾功能的治疗策略。还原论方法已经确定了几个抗增殖分子靶点,对用于调节这些靶点的领先小分子药物进行的有前景的临床前测试现已促成了具有里程碑意义的临床试验。然而,这种向靶向治疗的进展凸显了分子肾脏病学与分子肿瘤学治疗目标之间的重要差异,进而凸显了替代靶点活性在药物疗效中尚未得到充分理解的作用。阐明这些问题的系统研究应能加速这一有前景的治疗策略的发展。