Department of Physiology & Cellular Biophysics, The Clyde & Helen Wu Center for Molecular Cardiology, Columbia University Medical Center, New York, NY 10032, USA.
Pharmacogenomics. 2013 Sep;14(12):1517-26. doi: 10.2217/pgs.13.143.
The mTOR signaling pathway integrates inputs from a variety of upstream stimuli to regulate diverse cellular processes including proliferation, growth, survival, motility, autophagy, protein synthesis and metabolism. The mTOR pathway is dysregulated in a number of human pathologies including cancer, diabetes, obesity, autoimmune disorders, neurological disease and aging. Ongoing clinical trials testing mTOR-targeted treatments number in the hundreds and underscore its therapeutic potential. To date mTOR inhibitors are clinically approved to prevent organ rejection, to inhibit restenosis after angioplasty, and to treat several advanced cancers. In this review we discuss the continuously evolving field of mTOR pharmacogenomics, as well as highlight the emerging efforts in identifying diagnostic and prognostic markers, including miRNAs, in order to assess successful therapeutic responses.
mTOR 信号通路整合了来自多种上游刺激的输入,以调节多种细胞过程,包括增殖、生长、存活、运动、自噬、蛋白质合成和代谢。mTOR 通路在许多人类疾病中失调,包括癌症、糖尿病、肥胖、自身免疫性疾病、神经退行性疾病和衰老。目前正在进行的数百项临床试验测试 mTOR 靶向治疗方法,突显了其治疗潜力。迄今为止,mTOR 抑制剂已被临床批准用于预防器官排斥、抑制血管成形术后再狭窄以及治疗几种晚期癌症。在这篇综述中,我们讨论了 mTOR 药物基因组学不断发展的领域,并强调了在确定诊断和预后标志物(包括 miRNA)方面的新努力,以评估成功的治疗反应。