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Gene co-expression network approach for predicting prognostic microRNA biomarkers in different subtypes of breast cancer

机译:基因共表达网络方法预测乳腺癌不同亚型的预后微瘤生物标志物

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摘要

New diagnostic miRNA biomarkers for different types of cancer have been studied extensively, particularly for breast cancer (BC), which is a leading cause of death among women and has many different subtypes. In the present study, a systems biology approach was used to find remarkable and novel miRNA biomarkers for five molecular subtypes of BC: luminal A, luminal B, ERBB2, basal-like and normal-like. The mRNA expression data from the five BC subtypes was used to reconstruct co-expression networks. The important mRNA-miRNA interactions were considered when reconstructing the bipartite networks from which the five bipartite sub-networks were reconstructed for further analysis. The novel biomarkers detected for each subtype are as follows: miRNAs 26b-5p and 124-3p for basal-like, 26b-5p, 124-3p and 5011-5p for ERBB2, 26b-5p and 5011-5p for LumA, 124-3p, 26b-5p and 7-5p for LumB and 26b-5p, 124-3p and 193b-3p for normal-like. The roles of the identified miRNAs in the occurrence or development of each subtype of BC remain unclear and should be investigated in future studies. In addition, the target genes of these miRNAs may be critical to the mechanisms underlying each subtype and should be analyzed as therapeutic targets in future studies.
机译:已经广泛研究了用于不同类型癌症的新诊断miRNA生物标志物,特别是对于乳腺癌(BC),这是女性中死亡的主要原因,并且有许多不同的亚型。在本研究中,系统生物学方法用于寻找非易BC的五种分子亚型的非凡和新的miRNA生物标志物:腔A,腔B,ERBB2,基础样和正常样。来自五个BC子类型的mRNA表达数据用于重建共表达网络。当重建重建五个二分网网络的重建以进行进一步分析时,考虑了重要的mRNA-miRNA相互作用。对每个亚型检测的新型生物标志物如下:用于基础样,26b-5p,124-3p和5011-5p的MiRNA 26b-5p和124-3p用于ruma,26b-5p和5011-5p的5011-5p,124-用于螺母和26b-5p,124-3p和193b-3p的3p,26b-5p和7-5p用于正常样。所识别的miRNA在BC每个亚型的发生或开发中的作用仍然不清楚,应在未来的研究中调查。此外,这些miRNA的靶基因对于每个亚型的机制可能是至关重要的,并且应在未来的研究中被分析为治疗目标。

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