乳腺癌特异性蛋白相互作用网络的模式发现。

Xiaogang Wu, Scott H Harrison, Jake Yue Chen
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引用次数: 0

摘要

近年来,人们对早期乳腺癌(BRCA)检测的新生物标志物的兴趣日益浓厚。从网络生物学的角度来看,当今新兴的主题之一是重新表征蛋白质在其分子网络中的生物学功能。尽管已经提出了许多方法,包括用于发现分子生物标志物的基于网络的基因排序,以及用于发现功能模块的图聚类,但仍然很难发现隐藏在疾病特定分子网络中的系统级特性。我们以brca相关基因/蛋白为种子,重构了brca相关蛋白相互作用网络,并将其扩展到蛋白质相互作用数据库中。我们进一步开发了一个基于蚁群优化的计算框架来对网络节点进行排序。排序节点的任务被表示为在网络的所有节点上找到“蚁群”的最优密度分布的问题。我们的研究结果揭示了brca相关蛋白相互作用网络中一些有趣的系统水平模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pattern discovery in breast cancer specific protein interaction network.

Pattern discovery in breast cancer specific protein interaction network.

Pattern discovery in breast cancer specific protein interaction network.

Pattern discovery in breast cancer specific protein interaction network.

The interest in indentifying novel biomarkers for early stage breast cancer (BRCA) detection has become grown significantly in recent years. From a view of network biology, one of the emerging themes today is to re-characterize a protein's biological functions in its molecular network. Although many methods have been presented, including network-based gene ranking for molecular biomarker discovery, and graph clustering for functional module discovery, it is still hard to find systems-level properties hidden in disease specific molecular networks. We reconstructed BRCA-related protein interaction network by using BRCA-associated genes/proteins as seeds, and expanding them in an integrated protein interaction database. We further developed a computational framework based on Ant Colony Optimization to rank network nodes. The task of ranking nodes is represented as the problem of finding optimal density distributions of "ant colonies" on all nodes of the network. Our results revealed some interesting systems-level pattern in BRCA-related protein interaction network.

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