Proteomics and biomarkers in clinical trials for drug development

被引:52
|
作者
Lee, Jung-min [1 ]
Han, Jasmine J. [1 ]
Altwerger, Gary [1 ]
Kohn, Elise C. [1 ]
机构
[1] NCI, Mol Signaling Sect, Med Oncol Branch, Ctr Canc Res,NIH, Bethesda, MD 20892 USA
关键词
Proteomics; Biomarkers; Clinical trial; Drug development; Cancer; Targeted therapy; EPIDERMAL-GROWTH-FACTOR; CELL LUNG-CANCER; SURROGATE END-POINTS; ABL TYROSINE KINASE; OVARIAN-CANCER; FACTOR RECEPTOR; BREAST-CANCER; PHASE-II; COMBINATION THERAPY; PROGNOSTIC-FACTOR;
D O I
10.1016/j.jprot.2011.04.023
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Proteomics allows characterization of protein structure and function, protein-protein interactions, and peptide modifications. It has given us insight into the perturbations of signaling pathways within tumor cells and has improved the discovery of new therapeutic targets and possible indicators of response to and duration of therapy. The discovery, verification, and validation of novel biomarkers are critical in streamlining clinical development of targeted compounds, and directing rational treatments for patients whose tumors are dependent upon select signaling pathways. Studies are now underway in many diseases to examine the immune or inflammatory proteome, vascular proteome, cancer or disease proteome, and other subsets of the specific pathology microenvironment. Successful assay verification and biological validation of such biomarkers will speed development of potential agents to targetable dominant pathways and lead to selection of individuals most likely to benefit. Reconsideration of analytical and clinical trials methods for acquisition, examination, and translation of proteomics data must occur before we march further into future of drug development. Published by Elsevier B.V.
引用
收藏
页码:2632 / 2641
页数:10
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