Clustering protein-protein interaction network of TP53 tumor suppressor protein using Markov clustering algorithm

Thia Sabel Permata, A. Bustamam
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引用次数: 15

Abstract

The formation and proliferation of tumor cells occurs if a special protein that regulates cell division experience any changing on their function, gene expression or both of them. One of the tumor suppressor proteins that plays a significant role in controlling the cell cycle is the TP53 protein. In most of the genetic changes in the tumor, it found that mutant of TP53 is a high risk factor for cancer. Therefore, it is important to conduct studies on clustering protein-protein interactions (PPI) network of TP53. PPI networks are generally presented in the graph network with proteins as vertices and interactions as edges. Markov clustering (MCL) algorithm is a graph clustering method which based on a simulation of stochastic flow on a graph. In implementation, we applied MCL process using the Python programming language. The clustering datasets are the PPI of TP53 obtained from the STRING database. MCL algorithm consists of three main operations such as expansion, inflation, and prune. We conduct the clustering simulation using different parameter of expansion, inflation and the multiplier factor of identity matrix. As the results we found the MCL algorithm is proven to produce robust cluster with TP53 protein as a centroid for each clustering results.
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基于马尔可夫聚类算法的TP53肿瘤抑制蛋白聚类蛋白相互作用网络
如果调节细胞分裂的一种特殊蛋白质的功能、基因表达或两者发生变化,就会发生肿瘤细胞的形成和增殖。在控制细胞周期中起重要作用的肿瘤抑制蛋白之一是TP53蛋白。在大多数肿瘤的遗传变化中,发现TP53突变是癌症的高危因素。因此,对TP53的聚类蛋白-蛋白相互作用(PPI)网络进行研究具有重要意义。PPI网络通常在图网络中以蛋白质为顶点,相互作用为边。马尔可夫聚类(MCL)算法是一种基于在图上模拟随机流的图聚类方法。在实现中,我们使用Python编程语言应用MCL进程。聚类数据集为从STRING数据库中获得的TP53的PPI。MCL算法主要包括展开、膨胀和剪枝三种操作。采用不同的膨胀、膨胀参数和单位矩阵乘数因子进行聚类仿真。结果发现,MCL算法被证明可以产生以TP53蛋白为中心的鲁棒聚类。
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