发现复杂疾病治疗反应预测生物标志物的网络框架。

IF 3.4 3区 医学 Q1 PATHOLOGY
Uday S. Shanthamallu , Casey Kilpatrick , Alex Jones , Jonathan Rubin , Alif Saleh , Albert-László Barabási , Viatcheslav R. Akmaev , Susan D. Ghiassian
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引用次数: 0

摘要

与高通量多组学数据集中的分子特征数量相比,精准医疗在改变复杂的自身免疫性疾病治疗方面的潜力往往受到数据可用性有限和样本量不足的挑战。为解决这一问题,我们开发了新颖的 PRoBeNet(利用网络医学预测反应生物标志物)框架。ProBeNet 的运行假设是,药物的治疗效果会通过蛋白质-蛋白质相互作用网络传播,从而逆转疾病状态。ProBeNet 通过考虑以下因素来确定生物标志物的优先级:(1)治疗靶向蛋白;(2)疾病特异性分子特征;(3)细胞成分间相互作用的基本网络(人类相互作用组)。利用 ProBeNet 发现的生物标志物可预测患者对一种成熟的自身免疫疗法(英夫利昔单抗)和一种研究化合物(MAPK3/1 抑制剂)的反应。利用溃疡性结肠炎和类风湿性关节炎患者的回顾性基因表达数据以及溃疡性结肠炎和克罗恩病患者衍生组织的前瞻性数据验证了 ProBeNet 生物标记物的预测能力。使用 ProBeNet 生物标记物的机器学习模型明显优于使用所有基因或随机选择基因的模型,尤其是在数据有限(少于 20 个样本)的情况下。这些结果说明了 ProBeNet 在减少特征和在数据有限的情况下构建稳健的机器学习模型方面的价值。ProBeNet可用于为复杂的自身免疫性疾病疗法开发辅助和补充诊断测定,这有助于在临床试验中对合适的患者亚组进行分层,批准新药并改善患者预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Network-Based Framework to Discover Treatment-Response–Predicting Biomarkers for Complex Diseases

The potential of precision medicine to transform complex autoimmune disease treatment is often challenged by limited data availability and inadequate sample size when compared with the number of molecular features found in high-throughput multi-omics data sets. To address this issue, the novel framework PRoBeNet (Predictive Response Biomarkers using Network medicine) was developed. PRoBeNet operates under the hypothesis that the therapeutic effect of a drug propagates through a protein-protein interaction network to reverse disease states. PRoBeNet prioritizes biomarkers by considering i) therapy-targeted proteins, ii) disease-specific molecular signatures, and iii) an underlying network of interactions among cellular components (the human interactome). PRoBeNet helped discover biomarkers predicting patient responses to both an established autoimmune therapy (infliximab) and an investigational compound (a mitogen-activated protein kinase 3/1 inhibitor). The predictive power of PRoBeNet biomarkers was validated with retrospective gene-expression data from patients with ulcerative colitis and rheumatoid arthritis and prospective data from tissues from patients with ulcerative colitis and Crohn disease. Machine-learning models using PRoBeNet biomarkers significantly outperformed models using either all genes or randomly selected genes, especially when data were limited. These results illustrate the value of PRoBeNet in reducing features and for constructing robust machine-learning models when data are limited. PRoBeNet may be used to develop companion and complementary diagnostic assays, which may help stratify suitable patient subgroups in clinical trials and improve patient outcomes.

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来源期刊
CiteScore
8.10
自引率
2.40%
发文量
143
审稿时长
43 days
期刊介绍: The Journal of Molecular Diagnostics, the official publication of the Association for Molecular Pathology (AMP), co-owned by the American Society for Investigative Pathology (ASIP), seeks to publish high quality original papers on scientific advances in the translation and validation of molecular discoveries in medicine into the clinical diagnostic setting, and the description and application of technological advances in the field of molecular diagnostic medicine. The editors welcome for review articles that contain: novel discoveries or clinicopathologic correlations including studies in oncology, infectious diseases, inherited diseases, predisposition to disease, clinical informatics, or the description of polymorphisms linked to disease states or normal variations; the application of diagnostic methodologies in clinical trials; or the development of new or improved molecular methods which may be applied to diagnosis or monitoring of disease or disease predisposition.
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