Moran Michael F, Tong Jiefei, Taylor Paul, Ewing Robert M
Cancer Program, Hospital For Sick Children, and McLaughlin Centre for Molecular Medicine, and Banting and Best Department of Medical Research, University of Toronto, Ontario, Canada.
Biochim Biophys Acta. 2006 Dec;1766(2):230-41. doi: 10.1016/j.bbcan.2006.06.002. Epub 2006 Jun 23.
Protein phosphorylation is a key mechanism of cell regulation in normal and cancer cells. Various new cancer drugs and drug candidates are aimed at protein kinase targets. However, selecting patients likely to respond to these treatments, even among individuals with tumors expressing validated kinase targets remains a major challenge. There exists a need for biomarkers to facilitate the monitoring of modulation of drug-targeted kinase pathways. Phospho-proteomics involves the enrichment of phosphorylated proteins from tissue, and the application of technologies such as mass spectrometry (MS) for the identification and quantification of protein phosphorylation sites. It has potential to provide pharmacodynamic readouts of disease states and cellular drug responses in tumor samples, but technical hurdles and bioinformatics challenges will need to be addressed.
蛋白质磷酸化是正常细胞和癌细胞中细胞调节的关键机制。各种新型抗癌药物和候选药物都以蛋白激酶为靶点。然而,即使在表达已验证激酶靶点的肿瘤患者中,选择可能对这些治疗有反应的患者仍然是一项重大挑战。需要生物标志物来促进对药物靶向激酶途径调节的监测。磷酸化蛋白质组学涉及从组织中富集磷酸化蛋白质,并应用质谱(MS)等技术来鉴定和定量蛋白质磷酸化位点。它有潜力提供肿瘤样本中疾病状态和细胞药物反应的药效学读数,但技术障碍和生物信息学挑战仍需解决。