Office of Cancer Clinical Proteomics Research, Center for Strategic Scientific Initiative, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Proteomics Clin Appl. 2010 Dec;4(12):904-14. doi: 10.1002/prca.201000057. Epub 2010 Nov 22.
Proteomics holds great promise in personalized medicine for cancer in the post-genomic era. In the past decade, clinical proteomics has significantly evolved in terms of technology development, optimization and standardization, as well as in advanced bioinformatics data integration and analysis. Great strides have been made for characterizing a large number of proteins qualitatively and quantitatively in a proteome, including the use of sample fractionation, protein microarrays and MS. It is believed that differential proteomic analysis of high-quality clinical biospecimen (tissue and biofluids) can potentially reveal protein/peptide biomarkers responsible for cancer by means of their altered levels of expression and/or PTMs. Multiple reaction monitoring, a multiplexed platform using stable isotope dilution-MS with sensitivity and reproducibility approaching that of traditional ELISAs commonly used in the clinical setting, has emerged as a potentially promising technique for next-generation high-throughput protein biomarker measurements for diagnostics and therapeutics.
蛋白质组学在后基因组时代的癌症个性化医学中具有巨大的应用前景。在过去的十年中,临床蛋白质组学在技术发展、优化和标准化方面,以及在先进的生物信息学数据集成和分析方面都取得了显著的进展。通过使用样品分馏、蛋白质微阵列和 MS 等方法,对蛋白质组中的大量蛋白质进行定性和定量的描述已经取得了很大的进展。人们相信,对高质量临床生物样本(组织和生物流体)的差异蛋白质组学分析可以通过其改变的表达水平和/或 PTM 来揭示与癌症相关的蛋白质/肽生物标志物。多重反应监测是一种使用稳定同位素稀释-MS 的多重平台,其灵敏度和重现性接近传统 ELISA,通常用于临床环境,已成为下一代高通量蛋白质生物标志物诊断和治疗的潜在有前途的技术。