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首页> 外文期刊>European review for medical and pharmacological sciences. >Investigating key genes associated with ovarian cancer by integrating affinity propagation clustering and mutual information network analysis
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Investigating key genes associated with ovarian cancer by integrating affinity propagation clustering and mutual information network analysis

机译:通过结合亲和力传播聚类和互信息网络分析研究与卵巢癌相关的关键基因

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OBJECTIVE: The objective of the present work was to investigate key genes in ovarian cancer based on mAP-KL method which comprised the maxT multiple hypothesis (m), Krzanowski and Lai (KL) cluster quality index, and affinity propagation (AP) clustering algorithm, and mutual information network (MIN) constructed by the context likelihood of relatedness (CLR) algorithm. MATERIALS AND METHODS: MAP-KL method was employed to identify exemplars in ovarian cancer, of which the maxT function ranked the genes of train set and test set and obtained top 200 genes; KL cluster index was utilized to determine the quantity of clusters; and then AP clustering algorithm was conducted to identify the clusters and their exemplars. Also, we assessed the classification performance of mAP-KL by support vector machines (SVM) model. Subsequently, the MIN for exemplars and cluster genes was constructed according to CLR algorithm. Finally, topological centrality properties of exemplars in MIN were assessed to investigate key genes for ovarian cancer. RESULTS: SVM model validated that the classification between normal controls and ovarian cancer patients by mAP-KL had a good performance. A total of 22 clusters and exemplars were detected by performing the mAP-KL method. Based on the topological centrality analyses for exemplars in MIN, we considered the C9orf16, COX5B and ACTB to be key genes in the progress of ovarian cancer. CONCLUSIONS: We have obtained three key genes (C9orf16, COX5B and ACTB) for ovarian cancer on the basis of mAP-KL method and MIN analysis. These genes might be potential biomarkers for treatment of ovarian cancer, and give insight for revealing the underlying mechanism of this tumor.
机译:目的:本研究的目的是基于mAP-KL方法研究卵巢癌的关键基因,该方法包括maxT多重假设(m),Krzanowski和Lai(KL)簇质量指数以及亲和力传播(AP)簇算法,以及由相关性上下文相似性(CLR)算法构建的互信息网络(MIN)。材料与方法:MAP-KL法用于鉴定卵巢癌的样本,其中maxT功能对训练集和测试集的基因进行排名,并获得前200个基因。利用KL聚类指数确定聚类数量;然后进行AP聚类算法识别聚类及其实例。此外,我们通过支持向量机(SVM)模型评估了mAP-KL的分类性能。随后,根据CLR算法构建示例和簇基因的MIN。最后,评估了MIN中示例的拓扑中心性,以研究卵巢癌的关键基因。结果:SVM模型验证了mAP-KL对正常对照组和卵巢癌患者的分类效果良好。通过执行mAP-KL方法,共检测到22个簇和示例。基于MIN中示例的拓扑中心性分析,我们认为C9orf16,COX5B和ACTB是卵巢癌进展中的关键基因。结论:根据mAP-KL法和MIN分析,我们获得了卵巢癌的三个关键基因(C9orf16,COX5B和ACTB)。这些基因可能是治疗卵巢癌的潜在生物标志物,并有助于揭示该肿瘤的潜在机制。

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