This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Metastasis and subsequent resistance to tamoxifen therapy is a major cause of death in patients with breast cancer. Approximately 50% of patients with recurrent disease appear non-responsive to tamoxifen, resulting in progressive disease, while the other half shows objective response. Therapy-resistance is not fully understood and available predictors work only in ~50% of the cases. Clearly, new markers are needed to better predict therapy efficacy, and develop targets for new therapies. The ultimate goal of this study is to identify proteins that associate with therapy-resistance using high-resolution liquid chromatography coupled with high performance mass spectrometry (nanoLC-FTMS) and validate candidate biomarkers using targeted LC-MS approaches and immunohistochemistry.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR018522-08
Application #
8170707
Study Section
Special Emphasis Panel (ZRG1-BCMB-H (40))
Project Start
2010-07-01
Project End
2011-06-30
Budget Start
2010-07-01
Budget End
2011-06-30
Support Year
8
Fiscal Year
2010
Total Cost
$32,124
Indirect Cost
Name
Battelle Pacific Northwest Laboratories
Department
Type
DUNS #
032987476
City
Richland
State
WA
Country
United States
Zip Code
99352
Smallwood, Heather S; Duan, Susu; Morfouace, Marie et al. (2017) Targeting Metabolic Reprogramming by Influenza Infection for Therapeutic Intervention. Cell Rep 19:1640-1653
Wang, Hui; Barbieri, Christopher E; He, Jintang et al. (2017) Quantification of mutant SPOP proteins in prostate cancer using mass spectrometry-based targeted proteomics. J Transl Med 15:175
Sigdel, Tara K; Gao, Yuqian; He, Jintang et al. (2016) Mining the human urine proteome for monitoring renal transplant injury. Kidney Int 89:1244-52
Webb-Robertson, Bobbie-Jo M; Wiberg, Holli K; Matzke, Melissa M et al. (2015) Review, evaluation, and discussion of the challenges of missing value imputation for mass spectrometry-based label-free global proteomics. J Proteome Res 14:1993-2001
Ibrahim, Yehia M; Baker, Erin S; Danielson 3rd, William F et al. (2015) Development of a New Ion Mobility (Quadrupole) Time-of-Flight Mass Spectrometer. Int J Mass Spectrom 377:655-662
Ream, Thomas S; Haag, Jeremy R; Pontvianne, Frederic et al. (2015) Subunit compositions of Arabidopsis RNA polymerases I and III reveal Pol I- and Pol III-specific forms of the AC40 subunit and alternative forms of the C53 subunit. Nucleic Acids Res 43:4163-78
Depuydt, Geert; Xie, Fang; Petyuk, Vladislav A et al. (2014) LC-MS proteomics analysis of the insulin/IGF-1-deficient Caenorhabditis elegans daf-2(e1370) mutant reveals extensive restructuring of intermediary metabolism. J Proteome Res 13:1938-56
Merkley, Eric D; Metz, Thomas O; Smith, Richard D et al. (2014) The succinated proteome. Mass Spectrom Rev 33:98-109
He, Jintang; Sun, Xuefei; Shi, Tujin et al. (2014) Antibody-independent targeted quantification of TMPRSS2-ERG fusion protein products in prostate cancer. Mol Oncol 8:1169-80
Zhang, Qibin; Matzke, Melissa; Schepmoes, Athena A et al. (2014) High and low doses of ionizing radiation induce different secretome profiles in a human skin model. PLoS One 9:e92332

Showing the most recent 10 out of 350 publications