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EDRN Biomarker Reference and Resource Center with the Department of Energy


EMSL Project ID
43796

Abstract

The purpose of the Early Detection Research Network (EDRN) Biomarker Reference and Resource Center (BRRC) is to develop a multiplex quantitative MS-based method, based on LC-SRM-MS for simultaneous detection of ~50 prostate cancer biomarkers in tissue and body fluids; to conduct analytical and clinical validation studies, in collaboration with EDRN investigators; to estimate the utility of the developed assay(s) for early detection and diagnosis of prostate cancer; and to develop identical multiplex quantitative detection of biomarkers in additional cancers, pancreas and breast.

Project Details

Start Date
2011-04-18
End Date
2014-04-27
Status
Closed

Team

Principal Investigator

Tao Liu
Institution
Pacific Northwest National Laboratory

Team Members

Thomas Fillmore
Institution
Environmental Molecular Sciences Laboratory

Tujin Shi
Institution
Pacific Northwest National Laboratory

Fang Xie
Institution
Pacific Northwest National Laboratory

Mahmud Hossain
Institution
Pacific Northwest National Laboratory

Weijun Qian
Institution
Pacific Northwest National Laboratory

David Camp
Institution
Pacific Northwest National Laboratory

Karin Rodland
Institution
Pacific Northwest National Laboratory

Related Publications

Antibody-independent targeted quantification of TMPRSS2-ERG fusion protein products in prostate cancer

He J, X Sun, T Shi, AA Schepmoes, TL Fillmore, VA Petyuk, F Xie, R Zhao, MA Gritsenko, F Yang, N Kitabayashi, SS Chae, M Rubin, J Siddiqui, J Wei, AM Chinnaiyan, W Qian, RD Smith, J Kagan, S Srivastava, KD Rodland, T Liu, and DG Camp, II. 2014. "Antibody-independent Targeted Quantification of TMPRSS2-ERG Fusion Protein Products in Prostate Cancer." Molecular Oncology. doi:10.1016/j.molonc.2014.02.004

Long-Gradient Separations Coupled with Selected Reaction Monitoring for Highly Sensitive, Large Scale Targeted Protein Quantification in a Single Analysis

Shi T, TL Fillmore, Y Gao, R Zhao, J He, AA Schepmoes, CD Nicora, C Wu, JL Chambers, RJ Moore, J Kagan, S Srivastava, KD Rodland, T Liu, DG Camp, II, RD Smith, and W Qian. 2013. "Long-Gradient Separations Coupled with Selected Reaction Monitoring for Highly Sensitive, Large Scale Targeted Protein Quantification in a Single Analysis." Analytical Chemistry 85(19):9196-9203. doi:10.1021/ac402105s

Targeted Quantification of Low ng/mL Level Proteins in Human Serum without Immunoaffinity Depletion

Targeted quantification of low ng/mL level proteins in human serum without immunoaffinity depletion.
Shi T, Sun X, Gao Y, Fillmore TL, Schepmoes AA, Zhao R, He J, Moore RJ, Kagan J, Rodland KD, Liu T, Liu AY, Smith RD, Tang K, Camp DG 2nd, Qian WJ.
J Proteome Res. 2013 Jul 5;12(7):3353-61. doi: 10.1021/pr400178v. Epub 2013 Jun 13.
PMID: 23763644

Root protein profile changes induced by Al exposure in two rice cultivars differing in Al tolerance

Liu T, M Hossain, AA Schepmoes, TL Fillmore, LJ Sokoll, SR Kronewitter, G Izmirlian, T Shi, W Qian, R Leach, IM Thompson, DW Chan, RD Smith, J Kagan, S Srinivastava, KD Rodland, and DG Camp, II. 2012. "Analysis of Serum Total and Free PSA Using Immunoaffinity Depletion Coupled to SRM: Correlation with Clinical Immunoassay Tests." Journal of Proteomics. doi:doi: 10.1016/j.jprot.2012.09.035 [In Press]