区分耐多药肺结核和对药物敏感肺结核的分子指标以及潜在的治疗药物。

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shulin Song, Donghui Gan, Di Wu, Ting Li, Shiqian Zhang, Yibo Lu, Guanqiao Jin
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引用次数: 0

摘要

耐多药结核病(MDR-TB)问题给全球公共卫生带来了巨大挑战。令人遗憾的是,耐药结核病(DR-TB)的诊断往往需要较长的时间或较多的实验室资源。迅速识别耐药结核病尤其具有挑战性。为了确定表明多重耐药性的生物标志物,我们对 GSE147689 数据集进行了差异表达基因(DEG)筛选,并随后进行了基因富集分析。我们的分析共发现了 117 个 DEGs,它们集中在与免疫反应相关的通路中。我们采用了三种机器学习方法,即随机森林、决策树和支持向量机递归特征消除(SVM-RFE),根据特征重要性得分确定了前 10 个基因。在这三种方法中,A4GALT 和 S1PR1 被确定为共同基因,并被选为区分 MDR-TB 和药物敏感性结核病(DS-TB)的潜在分子标记。随后利用 GSE147690 数据集对这些标记进行了验证。研究结果表明,在训练数据集和测试数据集中,A4GALT 区分 MDR-TB 和 DS-TB 的曲线下面积(AUC)值分别为 0.8571 和 0.7121。在训练数据集和测试数据集中,S1PR1 的 AUC 值分别为 0.8163 和 0.5404。当把 A4GALT 和 S1PR1 结合在一起时,训练数据集和测试数据集的 AUC 值分别为 0.881 和 0.7551。利用单样本基因富集分析(ssGSEA)研究了中枢基因与浸润 MDR-TB 的 28 个免疫细胞之间的关系。研究结果表明,与 DS-TB 样本相比,MDR-TB 样本中 1 型 T 辅助细胞的比例较高,而活化树突状细胞的比例较低。A4GALT 与 1 型 T 辅助细胞呈负相关,而与活化树突状细胞呈正相关。S1PR1 与 1 型 T 辅助细胞呈正相关,而与活化树突状细胞呈负相关。此外,我们的研究利用连接图分析确定了包括维拉帕米在内的九种治疗 MDR-TB 的潜在药物。总之,我们的研究确定了区分 MDR-TB 和 DS-TB 的两个分子指标,并确定了治疗 MDR-TB 的九种潜在药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular Indicator for Distinguishing Multi-drug-Resistant Tuberculosis from Drug Sensitivity Tuberculosis and Potential Medications for Treatment.

The issue of multi-drug-resistant tuberculosis (MDR-TB) presents a substantial challenge to global public health. Regrettably, the diagnosis of drug-resistant tuberculosis (DR-TB) frequently necessitates an extended period or more extensive laboratory resources. The swift identification of MDR-TB poses a particularly challenging endeavor. To identify the biomarkers indicative of multi-drug resistance, we conducted a screening of the GSE147689 dataset for differentially expressed genes (DEGs) and subsequently conducted a gene enrichment analysis. Our analysis identified a total of 117 DEGs, concentrated in pathways related to the immune response. Three machine learning methods, namely random forest, decision tree, and support vector machine recursive feature elimination (SVM-RFE), were implemented to identify the top 10 genes according to their feature importance scores. A4GALT and S1PR1, which were identified as common genes among the three methods, were selected as potential molecular markers for distinguishing between MDR-TB and drug-susceptible tuberculosis (DS-TB). These markers were subsequently validated using the GSE147690 dataset. The findings suggested that A4GALT exhibited area under the curve (AUC) values of 0.8571 and 0.7121 in the training and test datasets, respectively, for distinguishing between MDR-TB and DS-TB. S1PR1 demonstrated AUC values of 0.8163 and 0.5404 in the training and test datasets, respectively. When A4GALT and S1PR1 were combined, the AUC values in the training and test datasets were 0.881 and 0.7551, respectively. The relationship between hub genes and 28 immune cells infiltrating MDR-TB was investigated using single sample gene enrichment analysis (ssGSEA). The findings indicated that MDR-TB samples exhibited a higher proportion of type 1 T helper cells and a lower proportion of activated dendritic cells in contrast to DS-TB samples. A negative correlation was observed between A4GALT and type 1 T helper cells, whereas a positive correlation was found with activated dendritic cells. S1PR1 exhibited a positive correlation with type 1 T helper cells and a negative correlation with activated dendritic cells. Furthermore, our study utilized connectivity map analysis to identify nine potential medications, including verapamil, for treating MDR-TB. In conclusion, our research identified two molecular indicators for the differentiation between MDR-TB and DS-TB and identified a total of nine potential medications for MDR-TB.

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来源期刊
Molecular Biotechnology
Molecular Biotechnology 医学-生化与分子生物学
CiteScore
4.10
自引率
3.80%
发文量
165
审稿时长
6 months
期刊介绍: Molecular Biotechnology publishes original research papers on the application of molecular biology to both basic and applied research in the field of biotechnology. Particular areas of interest include the following: stability and expression of cloned gene products, cell transformation, gene cloning systems and the production of recombinant proteins, protein purification and analysis, transgenic species, developmental biology, mutation analysis, the applications of DNA fingerprinting, RNA interference, and PCR technology, microarray technology, proteomics, mass spectrometry, bioinformatics, plant molecular biology, microbial genetics, gene probes and the diagnosis of disease, pharmaceutical and health care products, therapeutic agents, vaccines, gene targeting, gene therapy, stem cell technology and tissue engineering, antisense technology, protein engineering and enzyme technology, monoclonal antibodies, glycobiology and glycomics, and agricultural biotechnology.
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