Protein network construction using reverse phase protein array data

被引:4
|
作者
Varghese, Rency S. [1 ]
Zuo, Yiming [1 ,2 ]
Zhao, Yi [1 ,3 ]
Zhang, Yong-Wei [1 ]
Jablonski, Sandra A. [1 ]
Pierobon, Mariaelena [4 ]
Petricoin, Emanuel F. [4 ]
Ressom, Habtom W. [1 ]
Weiner, Louis M. [1 ]
机构
[1] Georgetown Univ, Lombardi Comprehens Canc Ctr, Dept Oncol, Washington, DC 20057 USA
[2] Virginia Polytech Inst & State Univ, Dept Elect & Comp Engn, Arlington, VA USA
[3] Brown Univ, Sch Publ Hlth, Dept Biostat, Providence, RI 02912 USA
[4] George Mason Univ, Ctr Appl Prote & Mol Med, Manassas, VA USA
关键词
RPPA; MANOVA; Network construction; Topology analysis; Breast cancer; PROGRESSION;
D O I
10.1016/j.ymeth.2017.06.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this paper, we introduce a novel computational method for constructing protein networks based on reverse phase protein array (RPPA) data to identify complex patterns in protein signaling. The method is applied to phosphoproteomic profiles of basal expression and activation/phosphorylation of 76 key signaling proteins in three breast cancer cell lines (MCF7, LCC1, and LCC9). Temporal RPPA data are acquired at 48 h, 96 h, and 144 h after knocking down four genes in separate experiments. These genes are selected from a previous study as important determinants for breast cancer survival. Interaction networks are constructed by analyzing the expression levels of protein pairs using a multivariate analysis of variance model. A new scoring criterion is introduced to determine relevant protein pairs. Through a network topology based analysis, we search for wiring patterns to identify key proteins that are associated with significant changes in expression levels across various experimental conditions. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:89 / 99
页数:11
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