The Proteomic Landscape of Triple-Negative Breast Cancer

被引:146
|
作者
Lawrence, Robert T. [1 ]
Perez, Elizabeth M. [1 ]
Hernandez, Daniel [1 ]
Miller, Chris P. [2 ,3 ]
Haas, Kelsey M. [1 ]
Irie, Hanna Y. [4 ]
Lee, Su-In [1 ,5 ]
Blau, C. Anthony [2 ,3 ]
Villen, Judit [1 ]
机构
[1] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
[2] Univ Washington, Ctr Canc Innovat, Seattle, WA 98109 USA
[3] Univ Washington, Div Hematol, Dept Med, Seattle, WA 98195 USA
[4] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
[5] Univ Washington, Dept Comp Sci & Engn, Seattle, WA 98195 USA
来源
CELL REPORTS | 2015年 / 11卷 / 04期
基金
美国国家科学基金会;
关键词
NF-KAPPA-B; DRUG-SENSITIVITY; TUMOR-GROWTH; CELL-LINES; PROTEIN; PROGRESSION; INHIBITION; MUTATIONS; GENOMICS; THERAPY;
D O I
10.1016/j.celrep.2015.03.050
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Triple-negative breast cancer is a heterogeneous disease characterized by poor clinical outcomes and a shortage of targeted treatment options. To discover molecular features of triple-negative breast cancer, we performed quantitative proteomics analysis of twenty human-derived breast cell lines and four primary breast tumors to a depth of more than 12,000 distinct proteins. We used this data to identify breast cancer subtypes at the protein level and demonstrate the precise quantification of biomarkers, signaling proteins, and biological pathways by mass spectrometry. We integrated proteomics data with exome sequence resources to identify genomic aberrations that affect protein expression. We performed a high-throughput drug screen to identify protein markers of drug sensitivity and understand the mechanisms of drug resistance. The genome and proteome provide complementary information that, when combined, yield a powerful engine for therapeutic discovery. This resource is available to the cancer research community to catalyze further analysis and investigation.
引用
收藏
页码:630 / 644
页数:15
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