Department of Biological and Medical Physics, Moscow Institute of Physics and Technology Dolgoprudny, Russia ; First Oncology Research and Advisory Center Moscow, Russia ; The Biogerontology Research Foundation London, UK ; Department of Experimental and Molecular Medicine, D. Rogachyov Federal Research Center of Pediatric Hematology, Oncology and Immunology Moscow, Russia.
Department of Biological and Medical Physics, Moscow Institute of Physics and Technology Dolgoprudny, Russia ; First Oncology Research and Advisory Center Moscow, Russia ; Department of Experimental and Molecular Medicine, D. Rogachyov Federal Research Center of Pediatric Hematology, Oncology and Immunology Moscow, Russia ; Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences Moscow, Russia.
Front Genet. 2014 Mar 3;5:49. doi: 10.3389/fgene.2014.00049. eCollection 2014.
The major challenges of aging research include absence of the comprehensive set of aging biomarkers, the time it takes to evaluate the effects of various interventions on longevity in humans and the difficulty extrapolating the results from model organisms to humans. To address these challenges we propose the in silico method for screening and ranking the possible geroprotectors followed by the high-throughput in vivo and in vitro validation. The proposed method evaluates the changes in the collection of activated or suppressed signaling pathways involved in aging and longevity, termed signaling pathway cloud, constructed using the gene expression data and epigenetic profiles of young and old patients' tissues. The possible interventions are selected and rated according to their ability to regulate age-related changes and minimize differences in the signaling pathway cloud. While many algorithmic solutions to simulating the induction of the old into young metabolic profiles in silico are possible, this flexible and scalable approach may potentially be used to predict the efficacy of the many drugs that may extend human longevity before conducting pre-clinical work and expensive clinical trials.
衰老研究的主要挑战包括缺乏全面的衰老生物标志物集、评估各种干预措施对人类寿命影响所需的时间,以及将模型生物的结果外推到人类的困难。为了应对这些挑战,我们提出了一种计算机筛选和排名可能的抗衰老药物的方法,然后进行高通量的体内和体外验证。该方法评估了参与衰老和长寿的激活或抑制信号通路的集合的变化,称为信号通路云,使用年轻和老年患者组织的基因表达数据和表观遗传谱构建。根据它们调节与年龄相关的变化的能力和最小化信号通路云中的差异来选择和评价可能的干预措施。虽然有许多算法解决方案可以在计算机上模拟诱导衰老进入年轻的代谢特征,但这种灵活和可扩展的方法可能可用于预测许多可能延长人类寿命的药物的疗效,然后再进行临床前工作和昂贵的临床试验。