Centre for Infection and Immunity, Queen's University Belfast, Belfast BT9 7BL, Northern Ireland, UK.
Genome Med. 2010 Dec 16;2(12):88. doi: 10.1186/gm209.
Cystic fibrosis is one of the most common life-limiting inherited disorders. Its clinical impact manifests chiefly in the lung, pancreas, gastrointestinal tract and sweat glands, with lung disease typically being most detrimental to health. The median age for survival has increased dramatically over the past decades, largely thanks to advances in understanding of the mechanisms and consequences of disease, leading to the development of better therapies and treatment regimes. The discovery of dysregulated protein biomarkers linked to cystic fibrosis has contributed considerably to this end. This article outlines clinical trials targeting known protein biomarkers, and the current and future contributions of proteomic techniques to cystic fibrosis research. The treatments described range from those designed to provide functional copies of the mutant protein responsible for cystic fibrosis, to others addressing the associated symptoms of chronic inflammation. Preclinical research has employed proteomics to help elucidate pathways and processes implicated in disease that might present opportunities for therapy or prognosis. Global analyses of cystic fibrosis have detected the differential expression of proteins involved in inflammation, proteolytic activity and oxidative stress, which are recognized symptoms of the cystic fibrosis phenotype. The dysregulation of other processes, such as the complement and mitochondrial systems, has also been implicated. A number of studies have focused specifically on proteins that interact with the cystic fibrosis protein, with the goal of restoring its normal proteostasis. Consequently, proteins involved in synthesis, folding, degradation, translocation and localization of the protein have been identified as potential therapeutic targets. Cystic fibrosis patients are prone to lung infections that are thought to contribute to chronic inflammation, and thus proteomic studies have also searched for microbiological biomarkers to use in early infection diagnosis or as indicators of virulence. The review concludes by proposing a future role for proteomics in the high-throughput validation of protein biomarkers under consideration as outcome measures for use in clinical trials and routine disease monitoring.
囊性纤维化是最常见的致死性遗传疾病之一。其临床表现主要涉及肺部、胰腺、胃肠道和汗腺,肺部疾病通常对健康的危害最大。在过去几十年中,由于对疾病机制和后果的认识不断提高,导致更好的治疗方法和治疗方案的发展,生存中位数年龄大幅提高。与囊性纤维化相关的失调蛋白生物标志物的发现为此做出了重要贡献。本文概述了针对已知蛋白生物标志物的临床试验,以及蛋白质组学技术对囊性纤维化研究的当前和未来贡献。所描述的治疗方法包括旨在提供负责囊性纤维化的突变蛋白的功能性副本的治疗方法,以及针对慢性炎症相关症状的其他治疗方法。临床前研究已经使用蛋白质组学来帮助阐明可能为治疗或预后提供机会的疾病相关途径和过程。对囊性纤维化的全球分析检测到涉及炎症、蛋白水解活性和氧化应激的蛋白质的差异表达,这些是囊性纤维化表型的公认症状。其他过程的失调,如补体和线粒体系统的失调,也被牵连进来。许多研究都专门针对与囊性纤维化蛋白相互作用的蛋白质,目的是恢复其正常的蛋白稳态。因此,参与蛋白质合成、折叠、降解、易位和定位的蛋白质已被确定为潜在的治疗靶点。囊性纤维化患者易患肺部感染,据认为这些感染会导致慢性炎症,因此蛋白质组学研究还寻找了微生物生物标志物,以用于早期感染诊断或作为毒力的指标。该综述最后提出了蛋白质组学在作为临床试验和常规疾病监测中使用的结果测量的候选蛋白生物标志物的高通量验证中的未来作用。