Hudler Petra, Kocevar Nina, Komel Radovan
Medical Centre for Molecular Biology, Institute of Biochemistry, Faculty of Medicine, University of Ljubljana, Vrazov trg 2, 1000 Ljubljana, Slovenia.
ScientificWorldJournal. 2014 Jan 14;2014:260348. doi: 10.1155/2014/260348. eCollection 2014.
Despite remarkable progress in proteomic methods, including improved detection limits and sensitivity, these methods have not yet been established in routine clinical practice. The main limitations, which prevent their integration into clinics, are high cost of equipment, the need for highly trained personnel, and last, but not least, the establishment of reliable and accurate protein biomarkers or panels of protein biomarkers for detection of neoplasms. Furthermore, the complexity and heterogeneity of most solid tumours present obstacles in the discovery of specific protein signatures, which could be used for early detection of cancers, for prediction of disease outcome, and for determining the response to specific therapies. However, cancer proteome, as the end-point of pathological processes that underlie cancer development and progression, could represent an important source for the discovery of new biomarkers and molecular targets for tailored therapies.
尽管蛋白质组学方法取得了显著进展,包括检测限和灵敏度的提高,但这些方法尚未在常规临床实践中得到应用。阻碍其融入临床的主要限制因素包括设备成本高昂、需要训练有素的人员,以及最后但同样重要的是,建立用于检测肿瘤的可靠且准确的蛋白质生物标志物或蛋白质生物标志物组合。此外,大多数实体瘤的复杂性和异质性给发现可用于癌症早期检测、疾病预后预测以及确定对特定疗法反应的特定蛋白质特征带来了障碍。然而,癌症蛋白质组作为癌症发生和发展基础病理过程的终点,可能是发现新生物标志物和定制疗法分子靶点的重要来源。