Park Kyunghyun, Kim Docyong, Ha Suhyun, Lee Doheon
Department of Bio and Brain Engineering, KAIST, 291 Daehak-ro, Yuseong-gu, Daejeon 305-701, Republic of Korea.
Department of Bio and Brain Engineering, KAIST, 291 Daehak-ro, Yuseong-gu, Daejeon 305-701, Republic of Korea; Bio-Synergy Research Center, KAIST, 291 Daehak-ro, Yuseong-gu, Daejeon 305-701, Republic of Korea.
PLoS One. 2015 Oct 15;10(10):e0140816. doi: 10.1371/journal.pone.0140816. eCollection 2015.
As pharmacodynamic drug-drug interactions (PD DDIs) could lead to severe adverse effects in patients, it is important to identify potential PD DDIs in drug development. The signaling starting from drug targets is propagated through protein-protein interaction (PPI) networks. PD DDIs could occur by close interference on the same targets or within the same pathways as well as distant interference through cross-talking pathways. However, most of the previous approaches have considered only close interference by measuring distances between drug targets or comparing target neighbors. We have applied a random walk with restart algorithm to simulate signaling propagation from drug targets in order to capture the possibility of their distant interference. Cross validation with DrugBank and Kyoto Encyclopedia of Genes and Genomes DRUG shows that the proposed method outperforms the previous methods significantly. We also provide a web service with which PD DDIs for drug pairs can be analyzed at http://biosoft.kaist.ac.kr/targetrw.
由于药效学药物相互作用(PD DDIs)可能会给患者带来严重的不良反应,因此在药物研发过程中识别潜在的PD DDIs非常重要。从药物靶点开始的信号通过蛋白质-蛋白质相互作用(PPI)网络进行传播。PD DDIs可能通过对相同靶点或同一途径的紧密干扰以及通过相互作用途径的远距离干扰而发生。然而,之前的大多数方法仅通过测量药物靶点之间的距离或比较靶点邻域来考虑紧密干扰。我们应用了带重启的随机游走算法来模拟从药物靶点开始的信号传播,以捕捉远距离干扰的可能性。与DrugBank和京都基因与基因组百科全书DRUG进行的交叉验证表明,所提出的方法明显优于之前的方法。我们还提供了一个网络服务,通过该服务可以在http://biosoft.kaist.ac.kr/targetrw上分析药物对的PD DDIs。