Department of Biochemistry, Yong Loo Lin School of Medicine, Singapore, Singapore.
Proteomics Clin Appl. 2007 Aug;1(8):820-33. doi: 10.1002/prca.200700169. Epub 2007 Jul 10.
Seventy million people suffer from diseases of the gastrointestinal tract annually in US, translating to US$85.5 billion in direct healthcare costs. The debilitating effects of these gastrointestinal (GI) diseases can be circumvented with good biomarkers for early detection of these disorders, which will greatly increase the success of curative treatments. GI fluids represent a potential reservoir of biomarkers for early diagnosis of various GI and systemic diseases since these fluids are the most proximal fluid bathing diseased cells. They are anticipated to have proteomes that closely reflect the ensemble of proteins secreted from the respective GI tissues. Most importantly, the disease markers present in GI fluids should be present in higher concentrations than in sera, thus offering greater sensitivity in their detection. However, proteome analysis of GI fluids can be complex mainly due to the dynamic range of protein content and the numerous PTMs of proteins in each specialized GI compartment. This review attempts to discuss the physiology of the various GI fluids, the special technical considerations required for proteome analysis of each fluid, as well as to summarize the current state of knowledge of biomarker discoveries and clinical utility of GI fluids such as salivary, gastric, pancreatic, and biliary secretions.
每年有 7000 万人患有美国胃肠道疾病,直接医疗费用达 855 亿美元。这些胃肠道(GI)疾病的衰弱影响可以通过对这些疾病进行早期检测的良好生物标志物来避免,这将大大提高治疗的成功率。GI 液代表了用于早期诊断各种 GI 和系统性疾病的潜在生物标志物库,因为这些液体是最接近患病细胞的液体。预计它们的蛋白质组将非常接近各自 GI 组织分泌的蛋白质的组合。最重要的是,GI 液中存在的疾病标志物的浓度应该高于血清中的浓度,从而在检测时具有更高的灵敏度。然而,GI 液的蛋白质组分析可能很复杂,主要是由于蛋白质含量的动态范围以及每个特殊 GI 隔室中蛋白质的许多翻译后修饰。本文综述了各种 GI 液的生理学,每种液体进行蛋白质组分析所需的特殊技术考虑因素,以及总结了 GI 液(如唾液、胃液、胰液和胆汁分泌液)中生物标志物发现和临床应用的最新知识。