Chignard Nicolas, Beretta Laura
Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.
Gastroenterology. 2004 Nov;127(5 Suppl 1):S120-5. doi: 10.1053/j.gastro.2004.09.025.
Refinements of serological markers and screening of patients at high risk for developing hepatocellular carcinoma (HCC) may lead to better HCC detection, earlier intervention, and successful treatment, improving long-term outcomes. Proteomics promises the discovery of biomarkers for early HCC detection and diagnosis. Proteomic-based profiling uniquely allows delineation of global changes in expression patterns resulting from transcriptional and posttranscriptional control, posttranslational modifications, and shifts in proteins between cellular compartments. Approaches to that effect include direct serum protein profiling and comparative analysis of protein expression in normal, precancerous, and early-stage tumor tissues. Identification of panels of tumor antigens that elicit a humoral response also may contribute to the discovery of new markers for HCC screening and diagnosis. Today, 2-dimensional polyacrylamide gel electrophoresis, multidimensional liquid chromatography, mass spectrometry, and protein microarrays are among the proteomic tools available for biomarker and drug target discovery. We review these technologies and their application to the study of HCC. Our objective is to provide a framework for appreciating the promise, while at the same time understanding the challenges behind translating proteomics discovery into novel diagnostic tests.
血清学标志物的改进以及对肝细胞癌(HCC)高危患者的筛查可能会带来更好的HCC检测、更早的干预和成功的治疗,从而改善长期预后。蛋白质组学有望发现用于早期HCC检测和诊断的生物标志物。基于蛋白质组学的分析能够独特地描绘出由转录和转录后控制、翻译后修饰以及细胞区室间蛋白质转移所导致的表达模式的整体变化。实现这一目标的方法包括直接血清蛋白质分析以及对正常、癌前和早期肿瘤组织中的蛋白质表达进行比较分析。识别引发体液反应的肿瘤抗原组也可能有助于发现用于HCC筛查和诊断的新标志物。如今,二维聚丙烯酰胺凝胶电泳、多维液相色谱、质谱分析和蛋白质微阵列是可用于生物标志物和药物靶点发现的蛋白质组学工具。我们综述了这些技术及其在HCC研究中的应用。我们的目标是提供一个框架,以便既能认识到其前景,同时又能理解将蛋白质组学发现转化为新型诊断测试背后的挑战。