| Literature DB >> 33389597 |
Bin Chen1,2, Mingjian Liu2, Zhenghong Chen2, Xiaorong Gao2, Yijun Cheng2, Yongxu Wei2, Zhebao Wu2, Hanbing Shang3.
Abstract
Intracerebral hemorrhage is a complicated disorder with limited proven prognostic and therapeutic targets and elusive mechanisms. With proteomic methods, we aimed to explore the global protein expression profile of perihematomal tissue from ICH patients and identify potential pathophysiological pathways and protein markers. Using iTRAQ-labeling quantitative proteomics technology, four ICH brain sample and four non-ICH brain samples were analyzed. Among the 3740 quantifiable proteins, 884 were dysregulated in the patients compared to those in the controls (p < 0.05). After bioinformatics analysis, the differentially expressed proteins were found to be mostly involved in hemostatic processes, nutrient metabolism signaling pathways, and antioxidation pathways. Moreover, fibronectin 1 was revealed to be at the center of the protein-protein interaction networks. In summary, the potential pathways and brain protein markers that could potentially be used to predict the prognosis of ICH were obtained from the altered proteomic profile of perihematomal tissue. Thus, these data may yield novel insights into the mechanisms of ICH-induced secondary brain injury.Entities:
Keywords: Brain proteomics; Fibronectin 1; Intracerebral hemorrhage; Mass spectrometry; iTRAQ
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Year: 2021 PMID: 33389597 DOI: 10.1007/s12017-020-08637-9
Source DB: PubMed Journal: Neuromolecular Med ISSN: 1535-1084 Impact factor: 3.843