Paweletz C P, Liotta L A, Petricoin E F
Tissue Proteomics Unit, Division of Therapeutic Proteins, Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, Maryland 20892, USA.
Urology. 2001 Apr;57(4 Suppl 1):160-3. doi: 10.1016/s0090-4295(00)00964-x.
The widespread use of serum markers during cancer screenings has led to the belief that there may be tumor markers yet to be discovered that offer better specificity and sensitivity than prostate-specific antigen (PSA). Proteomics, the analysis and characterization of global protein modifications, will add to our understanding of gene function and aid in biomarker and/or therapeutic target discovery. In the past, most proteomic studies were either performed using tumor cell lines or homogenized bulk tissue. Unfortunately, these approaches may not accurately reflect molecular events that take place in the actual ductal epithelium that change as a consequence of the malignant process. This report describes alternative proteomic-based approaches aimed at the identification of protein markers in the actual premalignant and frankly malignant epithelium.
血清标志物在癌症筛查中的广泛应用,使得人们相信可能存在尚未被发现的肿瘤标志物,其特异性和敏感性优于前列腺特异性抗原(PSA)。蛋白质组学,即对整体蛋白质修饰进行分析和表征,将增进我们对基因功能的理解,并有助于生物标志物和/或治疗靶点的发现。过去,大多数蛋白质组学研究要么使用肿瘤细胞系,要么使用匀浆的大块组织。不幸的是,这些方法可能无法准确反映在实际导管上皮中因恶性过程而发生变化的分子事件。本报告描述了基于蛋白质组学的替代方法,旨在鉴定实际癌前和明显恶性上皮中的蛋白质标志物。