Nguyen Nguyen T, Zhang Xiaolin, Wu Cathy, Lange Richard A, Chilton Robert J, Lindsey Merry L, Jin Yu-Fang
Department of Electrical and Computer Engineering, University of Texas at San Antonio, San Antonio, Texas, United States of America; San Antonio Cardiovascular Proteomics Center, University of Texas Health Science Center at San Antonio, San Antonio, Texas, United States of America.
Department of Electrical and Computer Engineering, University of Texas at San Antonio, San Antonio, Texas, United States of America.
PLoS Comput Biol. 2014 Mar 20;10(3):e1003472. doi: 10.1371/journal.pcbi.1003472. eCollection 2014 Mar.
Vast research efforts have been devoted to providing clinical diagnostic markers of myocardial infarction (MI), leading to over one million abstracts associated with "MI" and "Cardiovascular Diseases" in PubMed. Accumulation of the research results imposed a challenge to integrate and interpret these results. To address this problem and better understand how the left ventricle (LV) remodels post-MI at both the molecular and cellular levels, we propose here an integrative framework that couples computational methods and experimental data. We selected an initial set of MI-related proteins from published human studies and constructed an MI-specific protein-protein-interaction network (MIPIN). Structural and functional analysis of the MIPIN showed that the post-MI LV exhibited increased representation of proteins involved in transcriptional activity, inflammatory response, and extracellular matrix (ECM) remodeling. Known plasma or serum expression changes of the MIPIN proteins in patients with MI were acquired by data mining of the PubMed and UniProt knowledgebase, and served as a training set to predict unlabeled MIPIN protein changes post-MI. The predictions were validated with published results in PubMed, suggesting prognosticative capability of the MIPIN. Further, we established the first knowledge map related to the post-MI response, providing a major step towards enhancing our understanding of molecular interactions specific to MI and linking the molecular interaction, cellular responses, and biological processes to quantify LV remodeling.
大量的研究工作致力于提供心肌梗死(MI)的临床诊断标志物,这使得在PubMed上出现了超过100万篇与“MI”和“心血管疾病”相关的摘要。研究结果的积累给整合和解读这些结果带来了挑战。为了解决这个问题并更好地理解心肌梗死后左心室(LV)在分子和细胞水平上的重塑过程,我们在此提出一个将计算方法与实验数据相结合的综合框架。我们从已发表的人体研究中选择了一组初始的MI相关蛋白,并构建了一个MI特异性蛋白质-蛋白质相互作用网络(MIPIN)。对MIPIN的结构和功能分析表明,心肌梗死后的左心室在参与转录活性、炎症反应和细胞外基质(ECM)重塑的蛋白质方面表现出增加的代表性。通过对PubMed和UniProt知识库的数据挖掘,获取了MI患者中MIPIN蛋白已知的血浆或血清表达变化,并将其作为训练集来预测心肌梗死后未标记的MIPIN蛋白变化。这些预测通过PubMed上已发表的结果进行了验证,表明MIPIN具有预后能力。此外,我们建立了第一个与心肌梗死后反应相关的知识图谱,这朝着增强我们对MI特异性分子相互作用的理解以及将分子相互作用、细胞反应和生物过程联系起来以量化左心室重塑迈出了重要一步。