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蛋白质组学在理解脓毒症的生物学机制中的作用。

The role of proteomics in understanding biological mechanisms of sepsis.

机构信息

Department of Chemistry, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

Proteomics Clin Appl. 2014 Feb;8(1-2):35-52. doi: 10.1002/prca.201300101.

Abstract

Sepsis is a systemic inflammatory state caused by infection. Complications of this infection with multiple organ failure lead to more lethal conditions, such as severe sepsis and septic shock. Sepsis is one of the leading causes of US deaths. Novel biomarkers with high sensitivity and specificity may be helpful for early diagnosis of sepsis and for improvement of patient outcomes through the development of new therapies. Mass spectrometry-based proteomics offers powerful tools to identify such biomarkers and furthermore to give insight to fundamental mechanisms of this clinical condition. In this review, we summarize findings from proteomics studies of sepsis and how their applications have provided more understanding into the pathogenesis of septic infection. Literatures related to "proteomics", "sepsis", "systemic inflammatory response syndrome", "severe sepsis", "septic infection", and "multiple organ dysfunction syndrome" were searched using PubMed. Findings about neonatal and adult sepsis are discussed separately. Within the adult sepsis studies, results are grouped based on the models (e.g., human or animal). Across investigations in clinical populations and in rodent and mammalian animal models, biological pathways, such as inflammatory and acute phase response, coagulation, complement, mitochondrial energy metabolism, chaperones, and oxidative stress, are altered at the protein level. These proteomics studies have discovered many novel biomarker candidates of septic infection. Validation the clinical use of these biomarker candidates may significantly impact the diagnosis and prognosis of sepsis. In addition, the molecular mechanisms revealed by these studies may also guide the development of more effective treatments.

摘要

脓毒症是由感染引起的全身性炎症状态。这种感染引起的多器官衰竭并发症导致更致命的情况,如严重脓毒症和脓毒性休克。脓毒症是美国死亡的主要原因之一。具有高灵敏度和特异性的新型生物标志物可能有助于脓毒症的早期诊断,并通过开发新疗法改善患者的预后。基于质谱的蛋白质组学为识别这些生物标志物提供了强大的工具,并进一步深入了解这种临床情况的基本机制。在这篇综述中,我们总结了脓毒症蛋白质组学研究的发现,以及它们的应用如何为脓毒症感染的发病机制提供了更多的认识。使用 PubMed 搜索了与“蛋白质组学”、“脓毒症”、“全身炎症反应综合征”、“严重脓毒症”、“脓毒症感染”和“多器官功能障碍综合征”相关的文献。分别讨论了新生儿和成人脓毒症的发现。在成人脓毒症研究中,结果根据模型(例如,人类或动物)进行分组。在临床人群以及啮齿动物和哺乳动物动物模型中的研究中,蛋白质水平改变了炎症和急性期反应、凝血、补体、线粒体能量代谢、伴侣蛋白和氧化应激等生物学途径。这些蛋白质组学研究发现了许多脓毒症感染的新型生物标志物候选物。这些生物标志物候选物的临床应用验证可能会显著影响脓毒症的诊断和预后。此外,这些研究揭示的分子机制也可能指导更有效的治疗方法的开发。

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